Ligand source activities (1 row/activity)





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CHEMBL427807 213385 0 None 1 2 Human 9.7 pEC50 = 9.7 Functional
Activity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assayActivity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H]1CCCN1C(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CO)C(=O)N[C@H](C(N)=O)C(C)C)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)O)[C@@H](C)O 10.1021/jm990590f
57397279 69999 0 None - 1 Human 9.5 pEC50 = 9.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC(F)F)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939594 69999 0 None - 1 Human 9.5 pEC50 = 9.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC(F)F)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
127032015 138638 0 None - 1 Mouse 9.4 pEC50 = 9.4 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL 3561 116 51 45 -9.7 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](N)Cc2ccccc2)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775924 138638 0 None - 1 Mouse 9.4 pEC50 = 9.4 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL 3561 116 51 45 -9.7 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](N)Cc2ccccc2)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127032315 138428 0 None 1 2 Mouse 9.4 pEC50 = 9.4 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL 3880 126 55 49 -10.4 CCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3774395 138428 0 None 1 2 Mouse 9.4 pEC50 = 9.4 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL 3880 126 55 49 -10.4 CCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL4299295 213562 0 None 1 2 Mouse 9.4 pEC50 = 9.4 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
57390212 70007 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 367 5 0 5 4.5 CCC(CC)c1cc(C)n2nc(-c3c(C)cc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939601 70007 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 367 5 0 5 4.5 CCC(CC)c1cc(C)n2nc(-c3c(C)cc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
127030817 138507 0 None 1 2 Mouse 9.2 pEC50 = 9.2 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL 3824 122 55 49 -12.0 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3774939 138507 0 None 1 2 Mouse 9.2 pEC50 = 9.2 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL 3824 122 55 49 -12.0 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
57395433 69988 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 387 6 0 5 5.1 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(CC)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939583 69988 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 387 6 0 5 5.1 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(CC)c(=O)c12 10.1016/j.bmc.2011.11.015
11153312 65506 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 383 6 1 6 5.5 CCC(CC)n1ccc2c(Nc3ccc(OC)cc3Cl)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
CHEMBL1830523 65506 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 383 6 1 6 5.5 CCC(CC)n1ccc2c(Nc3ccc(OC)cc3Cl)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
127033542 138622 0 None 1 2 Mouse 9.1 pEC50 = 9.1 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL 3960 128 56 50 -10.4 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775796 138622 0 None 1 2 Mouse 9.1 pEC50 = 9.1 Functional
Antagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassayAntagonist activity at CRF-R1 in mouse AtT-20 cells assessed as inhibition of human CRF induced cAMP accumulation after 30 mins by radioimmunoassay
ChEMBL 3960 128 56 50 -10.4 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
25115057 69993 0 None - 1 Human 9.0 pEC50 = 9 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 399 6 0 5 5.4 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939588 69993 0 None - 1 Human 9.0 pEC50 = 9 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 399 6 0 5 5.4 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
57393713 69998 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 354 5 0 6 3.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939593 69998 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 354 5 0 6 3.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
57400682 70002 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 359 4 0 5 4.2 CCC(C)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939597 70002 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 359 4 0 5 4.2 CCC(C)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
145958142 162058 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Antagonist activity at human CRFR1 expressed in HEK293 cells assessed as inhibition of sauvagine-induced cAMP accumulation by measuring sauvagine EC50 at 1 uM after 30 mins (Rvb = 0.203 nM)Antagonist activity at human CRFR1 expressed in HEK293 cells assessed as inhibition of sauvagine-induced cAMP accumulation by measuring sauvagine EC50 at 1 uM after 30 mins (Rvb = 0.203 nM)
ChEMBL 383 6 1 6 4.8 CCCCN(CC)c1nc(C)nc2c1sc(=N)n2-c1c(C)cc(C)cc1C 10.1016/j.ejmech.2017.07.016
CHEMBL4160471 162058 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Antagonist activity at human CRFR1 expressed in HEK293 cells assessed as inhibition of sauvagine-induced cAMP accumulation by measuring sauvagine EC50 at 1 uM after 30 mins (Rvb = 0.203 nM)Antagonist activity at human CRFR1 expressed in HEK293 cells assessed as inhibition of sauvagine-induced cAMP accumulation by measuring sauvagine EC50 at 1 uM after 30 mins (Rvb = 0.203 nM)
ChEMBL 383 6 1 6 4.8 CCCCN(CC)c1nc(C)nc2c1sc(=N)n2-c1c(C)cc(C)cc1C 10.1016/j.ejmech.2017.07.016
57397276 69976 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 373 5 0 5 4.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939571 69976 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 373 5 0 5 4.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
57392001 69987 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 367 6 0 5 4.7 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939582 69987 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 367 6 0 5 4.7 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC)c(=O)c12 10.1016/j.bmc.2011.11.015
57393711 69975 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 353 5 0 5 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939570 69975 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 353 5 0 5 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
24758072 69977 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 320 4 0 2 6.1 CCC(CC)c1cc(C)n2nc(-c3ccc(C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939572 69977 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 320 4 0 2 6.1 CCC(CC)c1cc(C)n2nc(-c3ccc(C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
24758076 69981 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 380 7 0 4 6.1 CCc1cc(OC)c(OC)cc1-c1nn2c(C)cc(C(CC)CC)c2cc1C 10.1016/j.bmc.2011.11.015
CHEMBL1939576 69981 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 380 7 0 4 6.1 CCc1cc(OC)c(OC)cc1-c1nn2c(C)cc(C(CC)CC)c2cc1C 10.1016/j.bmc.2011.11.015
56665181 64760 0 None - 1 Human 7.0 pEC50 = 7 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 386 6 1 5 5.6 CCC(CC)Nc1c(C)c(C)nc2c(-c3ccc(OC)cc3Cl)c(C)nn12 10.1016/j.bmc.2011.07.055
CHEMBL1819085 64760 0 None - 1 Human 7.0 pEC50 = 7 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 386 6 1 5 5.6 CCC(CC)Nc1c(C)c(C)nc2c(-c3ccc(OC)cc3Cl)c(C)nn12 10.1016/j.bmc.2011.07.055
24758075 69982 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 350 5 0 4 5.3 CCC(CC)c1cc(C)n2nc(-c3cnc(N(C)C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939577 69982 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 350 5 0 4 5.3 CCC(CC)c1cc(C)n2nc(-c3cnc(N(C)C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
10024020 203102 0 None - 1 Human 6.0 pEC50 = 6.0 Functional
Effective dose against human Corticotropin releasing factor receptor 1 stimulated ACTH release from primary rat anterior pituitary cell culturesEffective dose against human Corticotropin releasing factor receptor 1 stimulated ACTH release from primary rat anterior pituitary cell cultures
ChEMBL 401 9 0 5 5.2 CCCN(c1nccc(-c2c(Cl)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL63989 203102 0 None - 1 Human 6.0 pEC50 = 6.0 Functional
Effective dose against human Corticotropin releasing factor receptor 1 stimulated ACTH release from primary rat anterior pituitary cell culturesEffective dose against human Corticotropin releasing factor receptor 1 stimulated ACTH release from primary rat anterior pituitary cell cultures
ChEMBL 401 9 0 5 5.2 CCCN(c1nccc(-c2c(Cl)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
56677028 65299 0 None - 1 Human 7.0 pEC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 359 7 2 6 4.7 CCC(CC)Nc1cc(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828886 65299 0 None - 1 Human 7.0 pEC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 359 7 2 6 4.7 CCC(CC)Nc1cc(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
44290322 101170 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Antagonist potency in hCRF1 stimulated adenylate cyclase assayAntagonist potency in hCRF1 stimulated adenylate cyclase assay
ChEMBL 382 8 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1021/jm990590f
CHEMBL295563 101170 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Antagonist potency in hCRF1 stimulated adenylate cyclase assayAntagonist potency in hCRF1 stimulated adenylate cyclase assay
ChEMBL 382 8 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1021/jm990590f
10178898 64741 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 396 6 1 6 5.4 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CSC2 10.1016/j.bmc.2011.07.055
CHEMBL1819065 64741 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 396 6 1 6 5.4 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CSC2 10.1016/j.bmc.2011.07.055
10024020 203102 0 None - 1 Human 5.8 pEC50 = 5.8 Functional
Effective dose against CRF stimulated cAMP production in CHO cells expressing human Corticotropin releasing factor receptor 1Effective dose against CRF stimulated cAMP production in CHO cells expressing human Corticotropin releasing factor receptor 1
ChEMBL 401 9 0 5 5.2 CCCN(c1nccc(-c2c(Cl)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL63989 203102 0 None - 1 Human 5.8 pEC50 = 5.8 Functional
Effective dose against CRF stimulated cAMP production in CHO cells expressing human Corticotropin releasing factor receptor 1Effective dose against CRF stimulated cAMP production in CHO cells expressing human Corticotropin releasing factor receptor 1
ChEMBL 401 9 0 5 5.2 CCCN(c1nccc(-c2c(Cl)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
57400680 69996 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 354 5 0 6 3.6 CCC(CC)c1cc(C)n2nc(-c3cnc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939591 69996 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 354 5 0 6 3.6 CCC(CC)c1cc(C)n2nc(-c3cnc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
10177704 64736 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 378 6 1 5 5.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819060 64736 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 378 6 1 5 5.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
56680359 65311 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 401 9 0 6 5.2 CCCN(CCC)c1cc(N(CC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828897 65311 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 401 9 0 6 5.2 CCCN(CCC)c1cc(N(CC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
57400681 70000 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 339 4 0 5 3.8 CCC(C)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939595 70000 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 339 4 0 5 3.8 CCC(C)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
24758074 69980 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 350 4 0 4 5.6 CCC(CC)c1cc(C)n2nc(-c3cc4c(cc3C)OCO4)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939575 69980 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 350 4 0 4 5.6 CCC(CC)c1cc(C)n2nc(-c3cc4c(cc3C)OCO4)c(C)cc12 10.1016/j.bmc.2011.11.015
25114821 69997 0 None -1 2 Rat 8.6 pEC50 = 8.6 Functional
Antagonist activity at rat CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at rat CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3cnc(OC(F)F)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939592 69997 0 None -1 2 Rat 8.6 pEC50 = 8.6 Functional
Antagonist activity at rat CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at rat CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3cnc(OC(F)F)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
10222795 64757 0 None - 1 Human 6.7 pEC50 = 6.7 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 402 5 1 4 6.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(Cl)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819082 64757 0 None - 1 Human 6.7 pEC50 = 6.7 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 402 5 1 4 6.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(Cl)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
56668632 64758 0 None - 1 Human 6.7 pEC50 = 6.7 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 434 7 1 5 6.0 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC(F)F)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819083 64758 0 None - 1 Human 6.7 pEC50 = 6.7 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 434 7 1 5 6.0 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC(F)F)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
56659877 65306 0 None - 1 Human 6.6 pEC50 = 6.6 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 415 9 1 6 5.9 CCCN(CCC)c1c(C(C)C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828892 65306 0 None - 1 Human 6.6 pEC50 = 6.6 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 415 9 1 6 5.9 CCCN(CCC)c1c(C(C)C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56683765 65505 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 388 8 0 7 4.2 CCCN(CCC)c1nc(N(C)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830522 65505 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 388 8 0 7 4.2 CCCN(CCC)c1nc(N(C)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56683688 65314 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 413 10 0 6 5.3 C=CCN(c1cc(N(CCC)CCC)n2nccc2n1)c1ccc(OC)cc1Cl 10.1016/j.bmc.2011.08.055
CHEMBL1828900 65314 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 413 10 0 6 5.3 C=CCN(c1cc(N(CCC)CCC)n2nccc2n1)c1ccc(OC)cc1Cl 10.1016/j.bmc.2011.08.055
25114821 69997 0 None 1 2 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3cnc(OC(F)F)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939592 69997 0 None 1 2 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3cnc(OC(F)F)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
24758071 69978 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 334 4 0 2 6.4 CCC(CC)c1cc(C)n2nc(-c3cc(C)c(C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939573 69978 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 334 4 0 2 6.4 CCC(CC)c1cc(C)n2nc(-c3cc(C)c(C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL429560 213540 0 None -2 2 Human 8.5 pEC50 = 8.5 Functional
Activity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assayActivity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCCN1C(=O)CNC(=O)[C@@H](N)CCC(N)=O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(N)=O 10.1021/jm990590f
CHEMBL2372650 210279 0 None 3 2 Human 8.5 pEC50 = 8.5 Functional
Activity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assayActivity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCCN1C(=O)[C@@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](N)CO)[C@@H](C)CC)[C@@H](C)O)C(C)C)[C@@H](C)CC)C(N)=O 10.1021/jm990590f
57398970 69990 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 403 7 1 6 4.0 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(CCO)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939585 69990 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 403 7 1 6 4.0 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(CCO)c(=O)c12 10.1016/j.bmc.2011.11.015
57402456 70009 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 353 4 0 5 4.1 CCC(C)c1cc(C)n2nc(-c3c(C)cc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939603 70009 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 353 4 0 5 4.1 CCC(C)c1cc(C)n2nc(-c3c(C)cc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
11588927 65507 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 377 7 1 6 5.4 CCc1cc(OC)ccc1Nc1nc2ccnn2c2c1ccn2C(CC)CC 10.1016/j.bmc.2011.08.055
CHEMBL1830524 65507 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 377 7 1 6 5.4 CCc1cc(OC)ccc1Nc1nc2ccnn2c2c1ccn2C(CC)CC 10.1016/j.bmc.2011.08.055
57397278 69992 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 379 6 0 5 5.0 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939587 69992 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 379 6 0 5 5.0 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
56659949 65508 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 381 6 1 5 6.0 CCc1cc(Cl)ccc1Nc1nc2ccnn2c2c1ccn2C(CC)CC 10.1016/j.bmc.2011.08.055
CHEMBL1830525 65508 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 381 6 1 5 6.0 CCc1cc(Cl)ccc1Nc1nc2ccnn2c2c1ccn2C(CC)CC 10.1016/j.bmc.2011.08.055
56678852 64759 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 372 6 1 5 5.3 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3Cl)c(C)nn12 10.1016/j.bmc.2011.07.055
CHEMBL1819084 64759 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 372 6 1 5 5.3 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3Cl)c(C)nn12 10.1016/j.bmc.2011.07.055
56670271 65509 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 360 5 0 4 5.6 CCC(CC)n1ccc2c(Cc3c(C)cc(C)cc3C)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
CHEMBL1830526 65509 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 360 5 0 4 5.6 CCC(CC)n1ccc2c(Cc3c(C)cc(C)cc3C)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
57400683 70006 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 353 4 0 6 3.3 CCC(C)c1cc(C)n2nc(-c3ccc(N(C)C)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939600 70006 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 353 4 0 6 3.3 CCC(C)c1cc(C)n2nc(-c3ccc(N(C)C)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
56659947 65498 0 None - 1 Human 6.4 pEC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 374 7 1 7 4.2 CCC(CC)Nc1cc(N(C)c2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830516 65498 0 None - 1 Human 6.4 pEC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 374 7 1 7 4.2 CCC(CC)Nc1cc(N(C)c2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL428505 213452 0 None - 1 Human 5.4 pEC50 = 5.4 Functional
Effective concentration to stimulate the human corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assayEffective concentration to stimulate the human corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(N)=O 10.1021/jm990590f
136042278 69986 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 359 5 1 4 4.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)[nH]c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939581 69986 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 359 5 1 4 4.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)[nH]c(=O)c12 10.1016/j.bmc.2011.11.015
11383650 65302 0 None 14 2 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828889 65302 0 None 14 2 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56668633 64761 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 400 6 1 6 4.9 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)CCO2 10.1016/j.bmc.2011.07.055
CHEMBL1819086 64761 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 400 6 1 6 4.9 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)CCO2 10.1016/j.bmc.2011.07.055
11552261 65510 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 361 5 1 5 5.7 CCC(CC)n1ccc2c(Nc3c(C)cc(C)cc3C)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
CHEMBL1830527 65510 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 361 5 1 5 5.7 CCC(CC)n1ccc2c(Nc3c(C)cc(C)cc3C)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
57400679 69989 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 383 7 1 6 3.7 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CCO)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939584 69989 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 383 7 1 6 3.7 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CCO)c(=O)c12 10.1016/j.bmc.2011.11.015
54754517 65496 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 417 10 0 7 4.8 CCCN(CCC)c1cc(N(COC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830514 65496 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 417 10 0 7 4.8 CCCN(CCC)c1cc(N(COC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
57398972 70008 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 339 3 0 5 3.8 COc1cc(C)c(-c2nn3c(C)cc(C(C)C)c3c(=O)n2C)c(C)c1 10.1016/j.bmc.2011.11.015
CHEMBL1939602 70008 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 339 3 0 5 3.8 COc1cc(C)c(-c2nn3c(C)cc(C(C)C)c3c(=O)n2C)c(C)c1 10.1016/j.bmc.2011.11.015
16126888 69974 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 336 5 0 3 5.8 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939569 69974 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 336 5 0 3 5.8 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
10376 2930 4 None 1 2 Human 7.4 pEC50 = 7.4 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
9801039 2930 4 None 1 2 Human 7.4 pEC50 = 7.4 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
CHEMBL1819077 2930 4 None 1 2 Human 7.4 pEC50 = 7.4 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
10376 2930 4 None -1 2 Rat 7.4 pEC50 = 7.4 Functional
Antagonist activity at rat corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at rat corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
9801039 2930 4 None -1 2 Rat 7.4 pEC50 = 7.4 Functional
Antagonist activity at rat corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at rat corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
CHEMBL1819077 2930 4 None -1 2 Rat 7.4 pEC50 = 7.4 Functional
Antagonist activity at rat corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at rat corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
56683763 65501 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
CHEMBL1830519 65501 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
10135150 64751 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 392 6 1 5 5.4 CCC(CC)Nc1c2c(nc3c(-c4cc(C)c(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819075 64751 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 392 6 1 5 5.4 CCC(CC)Nc1c2c(nc3c(-c4cc(C)c(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
57390211 69994 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 395 7 0 5 5.3 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC(C)C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939589 69994 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 395 7 0 5 5.3 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC(C)C)c(=O)c12 10.1016/j.bmc.2011.11.015
57398971 69995 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 393 7 0 5 5.1 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939590 69995 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 393 7 0 5 5.1 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
57397277 69991 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 381 6 0 5 5.3 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C(C)C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939586 69991 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 381 6 0 5 5.3 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C(C)C)c(=O)c12 10.1016/j.bmc.2011.11.015
57393714 70003 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 367 5 0 6 3.7 CCC(CC)c1cc(C)n2nc(-c3ccc(N(C)C)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939598 70003 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 367 5 0 6 3.7 CCC(CC)c1cc(C)n2nc(-c3ccc(N(C)C)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
11703582 65511 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 378 7 0 6 5.4 CCc1ccc(Oc2nc3ccnn3c3c2ccn3C(CC)CC)c(OC)c1 10.1016/j.bmc.2011.08.055
CHEMBL1830528 65511 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 378 7 0 6 5.4 CCc1ccc(Oc2nc3ccnn3c3c2ccn3C(CC)CC)c(OC)c1 10.1016/j.bmc.2011.08.055
56673724 65301 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 373 8 1 6 4.8 CCCN(CCC)c1cc(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828888 65301 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 373 8 1 6 4.8 CCCN(CCC)c1cc(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
57393712 69984 0 None - 1 Human 6.3 pEC50 = 6.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 337 5 0 4 5.2 CCC(CC)c1nc(C)n2nc(-c3ccc(OC)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939579 69984 0 None - 1 Human 6.3 pEC50 = 6.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 337 5 0 4 5.2 CCC(CC)c1nc(C)n2nc(-c3ccc(OC)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
56670270 65497 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 374 7 2 7 4.4 CCC(CC)Nc1c(C)c(Nc2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830515 65497 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 374 7 2 7 4.4 CCC(CC)Nc1c(C)c(Nc2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL2373995 210382 0 None -4 2 Human 8.2 pEC50 = 8.2 Functional
Activity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assayActivity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCCN1C(=O)N[C@@H](CC(=O)O)C(=O)[C@H](CC(=O)O)NC(=O)[C@@H](N)CC(N)=O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(N)=O)C(C)C 10.1021/jm990590f
24758073 69979 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 364 7 0 3 6.5 CCOc1ccc(-c2nn3c(C)cc(C(CC)CC)c3cc2C)c(CC)c1 10.1016/j.bmc.2011.11.015
CHEMBL1939574 69979 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 364 7 0 3 6.5 CCOc1ccc(-c2nn3c(C)cc(C(CC)CC)c3cc2C)c(CC)c1 10.1016/j.bmc.2011.11.015
22177839 64737 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 380 6 1 6 4.6 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCO2 10.1016/j.bmc.2011.07.055
CHEMBL1819061 64737 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 380 6 1 6 4.6 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCO2 10.1016/j.bmc.2011.07.055
22177742 64762 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 400 6 1 6 5.0 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)COC2 10.1016/j.bmc.2011.07.055
CHEMBL1819087 64762 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 400 6 1 6 5.0 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)COC2 10.1016/j.bmc.2011.07.055
136042277 69985 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 339 5 1 4 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)[nH]c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939580 69985 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 339 5 1 4 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)[nH]c(=O)c12 10.1016/j.bmc.2011.11.015
57402455 70001 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 345 3 0 5 3.8 COc1ccc(-c2nn3c(C)cc(C(C)C)c3c(=O)n2C)c(Cl)c1 10.1016/j.bmc.2011.11.015
CHEMBL1939596 70001 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as CRF-stimulated cAMP accumulation by enzyme immunoassay
ChEMBL 345 3 0 5 3.8 COc1ccc(-c2nn3c(C)cc(C(C)C)c3c(=O)n2C)c(Cl)c1 10.1016/j.bmc.2011.11.015
54754515 65300 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 373 7 2 6 5.0 CCC(CC)Nc1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828887 65300 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 373 7 2 6 5.0 CCC(CC)Nc1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
9970050 64740 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 380 6 1 6 4.7 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)COC2 10.1016/j.bmc.2011.07.055
CHEMBL1819064 64740 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 380 6 1 6 4.7 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)COC2 10.1016/j.bmc.2011.07.055
56670201 65312 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 415 10 0 6 5.6 CCCN(CCC)c1cc(N(CCC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828898 65312 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 415 10 0 6 5.6 CCCN(CCC)c1cc(N(CCC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56663414 65504 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 401 9 0 6 5.2 CCCN(CCC)c1cc(N(CC)c2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
CHEMBL1830521 65504 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 401 9 0 6 5.2 CCCN(CCC)c1cc(N(CC)c2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
56668634 64763 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 400 6 1 6 4.9 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)OCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819088 64763 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 400 6 1 6 4.9 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)OCC2 10.1016/j.bmc.2011.07.055
54754516 65304 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 401 9 1 6 5.3 CCCN(CCC)c1c(CC)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828890 65304 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 401 9 1 6 5.3 CCCN(CCC)c1c(CC)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
10111139 64752 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 392 6 1 5 5.4 CCC(CC)Nc1c2c(nc3c(-c4c(C)cc(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819076 64752 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 392 6 1 5 5.4 CCC(CC)Nc1c2c(nc3c(-c4c(C)cc(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
11383650 65302 0 None -14 2 Rat 7.1 pEC50 = 7.1 Functional
Antagonist activity at rat CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at rat CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828889 65302 0 None -14 2 Rat 7.1 pEC50 = 7.1 Functional
Antagonist activity at rat CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at rat CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56663337 65313 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 427 10 0 6 5.7 C=C(C)CN(c1cc(N(CCC)CCC)n2nccc2n1)c1ccc(OC)cc1Cl 10.1016/j.bmc.2011.08.055
CHEMBL1828899 65313 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 427 10 0 6 5.7 C=C(C)CN(c1cc(N(CCC)CCC)n2nccc2n1)c1ccc(OC)cc1Cl 10.1016/j.bmc.2011.08.055
56673725 65309 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 403 9 1 7 4.8 CCCN(CCC)c1c(OC)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828895 65309 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 403 9 1 7 4.8 CCCN(CCC)c1c(OC)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56683762 65500 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 388 8 0 7 4.2 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830518 65500 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 388 8 0 7 4.2 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
56659948 65499 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 388 8 1 7 4.5 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830517 65499 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 388 8 1 7 4.5 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1077301 208491 0 None -8 3 Human 8.0 pEC50 = 8.0 Functional
Activity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assayActivity of peptidic agonists on corticotropin releasing factor receptor using agonist-stimulated adenylate cyclase assay
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CO)[C@@H](C)CC)[C@@H](C)O)C(C)C)[C@@H](C)O)C(=O)N[C@@H](C)C(N)=O 10.1021/jm990590f
22177924 64747 0 None - 1 Human 6.0 pEC50 = 6.0 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 362 5 1 4 5.4 CCC(CC)Nc1c2c(nc3c(-c4ccc(C)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819071 64747 0 None - 1 Human 6.0 pEC50 = 6.0 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 362 5 1 4 5.4 CCC(CC)Nc1c2c(nc3c(-c4ccc(C)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
56663335 65305 0 None - 1 Human 7.0 pEC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 415 10 1 6 5.7 CCCc1c(Nc2ccc(OC)cc2Cl)nc2ccnn2c1N(CCC)CCC 10.1016/j.bmc.2011.08.055
CHEMBL1828891 65305 0 None - 1 Human 7.0 pEC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 415 10 1 6 5.7 CCCc1c(Nc2ccc(OC)cc2Cl)nc2ccnn2c1N(CCC)CCC 10.1016/j.bmc.2011.08.055
56663336 65310 0 None - 1 Human 7.0 pEC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 387 8 0 6 4.8 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828896 65310 0 None - 1 Human 7.0 pEC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP accumulation after 15 mins by cAMP enzyme immunoassay
ChEMBL 387 8 0 6 4.8 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
9865575 203397 1 None - 1 Human 6.0 pEC50 = 6.0 Functional
Effective dose against human Corticotropin releasing factor receptor 1 stimulated ACTH release from primary rat anterior pituitary cell culturesEffective dose against human Corticotropin releasing factor receptor 1 stimulated ACTH release from primary rat anterior pituitary cell cultures
ChEMBL 397 10 0 6 4.6 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL65484 203397 1 None - 1 Human 6.0 pEC50 = 6.0 Functional
Effective dose against human Corticotropin releasing factor receptor 1 stimulated ACTH release from primary rat anterior pituitary cell culturesEffective dose against human Corticotropin releasing factor receptor 1 stimulated ACTH release from primary rat anterior pituitary cell cultures
ChEMBL 397 10 0 6 4.6 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
9865575 203397 1 None - 1 Human 6.0 pEC50 = 6 Functional
Effective dose against CRF stimulated cAMP production in CHO cells expressing human Corticotropin releasing factor receptor 1Effective dose against CRF stimulated cAMP production in CHO cells expressing human Corticotropin releasing factor receptor 1
ChEMBL 397 10 0 6 4.6 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL65484 203397 1 None - 1 Human 6.0 pEC50 = 6 Functional
Effective dose against CRF stimulated cAMP production in CHO cells expressing human Corticotropin releasing factor receptor 1Effective dose against CRF stimulated cAMP production in CHO cells expressing human Corticotropin releasing factor receptor 1
ChEMBL 397 10 0 6 4.6 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL2370939 209963 0 None 5 2 Human 9.6 pIC50 = 9.6 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@](C)(CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]1CCC(=O)NNC(=O)C[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@](C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](C)NC(=O)[C@@H](C)NC1=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm0202122
10408534 76210 0 None - 1 Rat 9.2 pIC50 = 9.2 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 397 5 0 5 5.1 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058338 76210 0 None - 1 Rat 9.2 pIC50 = 9.2 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 397 5 0 5 5.1 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL1794009 208935 0 None -1 2 Human 9.1 pIC50 = 9.1 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](N)Cc1ccccc1)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@H](C)CC)[C@H](C)CC)NC(=O)[C@@H](Cc2c[nH]cn2)NC(=O)[C@H](C)NC1=O 10.1021/jm0202122
9979210 76287 0 None - 1 Rat 9.1 pIC50 = 9.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 414 5 0 5 5.0 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(N(C)C)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058596 76287 0 None - 1 Rat 9.1 pIC50 = 9.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 414 5 0 5 5.0 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(N(C)C)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL439883 213849 0 None -1 5 Human 9.1 pIC50 = 9.1 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm0202122
44362115 1169 0 None 2 6 Human 9.0 pIC50 = 9 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None None 10.1021/jm0202122
6967 1169 0 None 2 6 Human 9.0 pIC50 = 9 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None None 10.1021/jm0202122
CHEMBL1201609 1169 0 None 2 6 Human 9.0 pIC50 = 9 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None None 10.1021/jm0202122
CHEMBL440057 1169 0 None 2 6 Human 9.0 pIC50 = 9 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None None 10.1021/jm0202122
44587375 193400 0 None - 1 Human 9.0 pIC50 = 9 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 393 9 0 6 4.8 CCCN(CCC)c1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL525716 193400 0 None - 1 Human 9.0 pIC50 = 9 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 393 9 0 6 4.8 CCCN(CCC)c1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
70688491 76289 0 None - 1 Rat 9.0 pIC50 = 9.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 397 5 0 5 5.1 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(Cl)cc3OC)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058598 76289 0 None - 1 Rat 9.0 pIC50 = 9.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 397 5 0 5 5.1 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(Cl)cc3OC)ccnc21 10.1016/j.bmcl.2012.06.034
44610627 139975 0 None -1 2 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production preincubated for 30 mins followed by CRF addition measured after 30 mins by HTRF assayAntagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production preincubated for 30 mins followed by CRF addition measured after 30 mins by HTRF assay
ChEMBL 519 9 2 8 5.5 Cc1cc(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccccc3)C3CC3)c2=O)c(C)nc1OC(F)F 10.1016/j.bmcl.2016.03.067
CHEMBL3799870 139975 0 None -1 2 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production preincubated for 30 mins followed by CRF addition measured after 30 mins by HTRF assayAntagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production preincubated for 30 mins followed by CRF addition measured after 30 mins by HTRF assay
ChEMBL 519 9 2 8 5.5 Cc1cc(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccccc3)C3CC3)c2=O)c(C)nc1OC(F)F 10.1016/j.bmcl.2016.03.067
70690504 76083 0 None - 1 Rat 8.8 pIC50 = 8.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 417 6 0 6 4.2 COCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2057479 76083 0 None - 1 Rat 8.8 pIC50 = 8.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 417 6 0 6 4.2 COCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
70682137 76284 0 None - 1 Rat 8.8 pIC50 = 8.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 401 5 0 5 4.9 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058593 76284 0 None - 1 Rat 8.8 pIC50 = 8.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 401 5 0 5 4.9 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
45483574 198034 0 None -2 2 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production after 30 mins by HTRF analysisAntagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production after 30 mins by HTRF analysis
ChEMBL 425 8 1 8 3.4 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C#N)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
CHEMBL573978 198034 0 None -2 2 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production after 30 mins by HTRF analysisAntagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production after 30 mins by HTRF analysis
ChEMBL 425 8 1 8 3.4 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C#N)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
44194976 195934 0 None -7 2 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production by HTRF methodAntagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production by HTRF method
ChEMBL 377 7 1 6 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL559437 195934 0 None -7 2 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production by HTRF methodAntagonist activity at CRF1 receptor in human Y79 cells assessed as inhibition of CRF-stimulated cAMP production by HTRF method
ChEMBL 377 7 1 6 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL2370938 209962 0 None -2 2 Human 8.7 pIC50 = 8.7 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@](C)(CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCNC(C)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@](C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm0202122
9884878 173025 18 None - 1 Human 8.0 pIC50 = 8 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmc.2011.07.055
CHEMBL45187 173025 18 None - 1 Human 8.0 pIC50 = 8 Functional
Antagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassayAntagonist activity at human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells assessed as inhibition of CRF-induced cAMP production after 15 mins by enzyme immunoassay
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmc.2011.07.055
CHEMBL2369741 209665 0 None -2 2 Human 8.0 pIC50 = 8.0 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](N)Cc1ccccc1)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC)NC(=O)[C@@H](C)NC(=O)[C@H](CCC(N)=O)NC1=O 10.1021/jm0202122
21984762 77542 0 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 409 8 0 4 5.9 CCc1nn2c(-c3ccc(OC)cc3Cl)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087550 77542 0 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 409 8 0 4 5.9 CCc1nn2c(-c3ccc(OC)cc3Cl)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
21984648 77544 0 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 389 8 0 4 5.5 CCc1nn2c(-c3ccc(C)cc3OC)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087552 77544 0 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 389 8 0 4 5.5 CCc1nn2c(-c3ccc(C)cc3OC)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
10378 3985 37 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 10.1016/j.bmcl.2010.10.095
11596613 3985 37 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 10.1016/j.bmcl.2010.10.095
CHEMBL1287935 3985 37 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 10.1016/j.bmcl.2010.10.095
DB12512 3985 37 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 10.1016/j.bmcl.2010.10.095
11509708 18992 3 None - 1 Human 6.0 pIC50 = 6 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 CC[C@@H](Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
CHEMBL1287905 18992 3 None - 1 Human 6.0 pIC50 = 6 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 CC[C@@H](Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
58317452 126486 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 424 5 2 2 6.1 CC(Nc1ccccc1)[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3652065 126486 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 424 5 2 2 6.1 CC(Nc1ccccc1)[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
10044263 76291 0 None - 1 Rat 8.0 pIC50 = 8.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 363 5 0 5 4.4 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058600 76291 0 None - 1 Rat 8.0 pIC50 = 8.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 363 5 0 5 4.4 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
9820671 188818 0 None -6 2 Rat 7.0 pIC50 = 7.0 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 369 6 1 7 3.9 CC[C@@H](C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL506214 188818 0 None -6 2 Rat 7.0 pIC50 = 7.0 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 369 6 1 7 3.9 CC[C@@H](C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
58801661 77565 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 495 11 0 8 4.8 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(OC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087573 77565 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 495 11 0 8 4.8 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(OC)nn23)c(OC)c1 10.1021/jm300259r
53357662 126532 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 447 4 1 3 5.8 Cc1nn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c(C)c1Cl nan
CHEMBL3652110 126532 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 447 4 1 3 5.8 Cc1nn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c(C)c1Cl nan
58317263 126528 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 435 4 1 3 5.7 O=C(N[C@H]1CC[C@H](Cn2ncc3ccccc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652106 126528 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 435 4 1 3 5.7 O=C(N[C@H]1CC[C@H](Cn2ncc3ccccc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
58398961 136333 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 431 4 1 4 4.6 Cn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)ccc3Cl)CC2)c2ccccc21 nan
CHEMBL3731086 136333 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 431 4 1 4 4.6 Cn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)ccc3Cl)CC2)c2ccccc21 nan
CHEMBL3734018 136333 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 431 4 1 4 4.6 Cn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)ccc3Cl)CC2)c2ccccc21 nan
58317281 126521 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 415 5 3 4 4.2 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CNc2cc(C(F)(F)F)n[nH]2)CC1 nan
CHEMBL3652099 126521 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 415 5 3 4 4.2 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CNc2cc(C(F)(F)F)n[nH]2)CC1 nan
CHEMBL2369693 209647 0 None -1 2 Human 6.9 pIC50 = 6.9 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](N)Cc1ccccc1)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@H](C)NC1=O 10.1021/jm0202122
53308745 135574 0 None 67 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 441 4 1 3 4.6 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C3(CC3)c3cc(F)ccc32)CC1 nan
CHEMBL3729075 135574 0 None 67 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 441 4 1 3 4.6 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C3(CC3)c3cc(F)ccc32)CC1 nan
44446725 168953 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2008.07.063
CHEMBL438888 168953 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2008.07.063
CHEMBL2370930 209959 0 None -1 2 Human 7.9 pIC50 = 7.9 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](N)Cc1ccccc1)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC1=O 10.1021/jm0202122
60155991 77579 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 515 12 0 9 4.8 COCCN(CC1CCOCC1)c1c(SC)nn2c(-c3c(OC)cc(COC)cc3OC)cccc12 10.1021/jm300259r
CHEMBL2087801 77579 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 515 12 0 9 4.8 COCCN(CC1CCOCC1)c1c(SC)nn2c(-c3c(OC)cc(COC)cc3OC)cccc12 10.1021/jm300259r
59186840 126461 0 None - 1 Human 5.9 pIC50 = 5.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 468 7 2 4 5.2 CN(C)Cc1ccc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)nc1 nan
CHEMBL3652040 126461 0 None - 1 Human 5.9 pIC50 = 5.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 468 7 2 4 5.2 CN(C)Cc1ccc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)nc1 nan
53341220 135576 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 444 4 1 2 5.6 CC1(C)C(=O)N(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)ccc3Cl)CC2)c2ccccc21 nan
CHEMBL3729078 135576 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 444 4 1 2 5.6 CC1(C)C(=O)N(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)ccc3Cl)CC2)c2ccccc21 nan
10379 3059 39 None -1 3 Rat 6.9 pIC50 = 6.9 Functional
Antagonist activity at CRF1 receptor in rat pituitary cells assessed as inhibition of CRF-mediated ACTH productionAntagonist activity at CRF1 receptor in rat pituitary cells assessed as inhibition of CRF-mediated ACTH production
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
9884366 3059 39 None -1 3 Rat 6.9 pIC50 = 6.9 Functional
Antagonist activity at CRF1 receptor in rat pituitary cells assessed as inhibition of CRF-mediated ACTH productionAntagonist activity at CRF1 receptor in rat pituitary cells assessed as inhibition of CRF-mediated ACTH production
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
CHEMBL482950 3059 39 None -1 3 Rat 6.9 pIC50 = 6.9 Functional
Antagonist activity at CRF1 receptor in rat pituitary cells assessed as inhibition of CRF-mediated ACTH productionAntagonist activity at CRF1 receptor in rat pituitary cells assessed as inhibition of CRF-mediated ACTH production
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
DB12572 3059 39 None -1 3 Rat 6.9 pIC50 = 6.9 Functional
Antagonist activity at CRF1 receptor in rat pituitary cells assessed as inhibition of CRF-mediated ACTH productionAntagonist activity at CRF1 receptor in rat pituitary cells assessed as inhibition of CRF-mediated ACTH production
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
44621879 126491 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 443 5 2 3 5.6 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)ncc1F nan
CHEMBL3652070 126491 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 443 5 2 3 5.6 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)ncc1F nan
70694747 76293 0 None - 1 Rat 6.9 pIC50 = 6.9 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 377 5 0 5 4.8 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(OC)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058602 76293 0 None - 1 Rat 6.9 pIC50 = 6.9 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 377 5 0 5 4.8 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(OC)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
70686533 76618 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2063381 76618 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmc.2012.09.028
70686533 76618 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063381 76618 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmcl.2012.07.047
44814766 126482 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 342 5 2 2 4.7 O=C(N[C@H]1CC[C@H](CNc2ccccc2)CC1)c1cccc(Cl)c1 nan
CHEMBL3652061 126482 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 342 5 2 2 4.7 O=C(N[C@H]1CC[C@H](CNc2ccccc2)CC1)c1cccc(Cl)c1 nan
53341553 136020 0 None 331 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 459 4 1 3 5.3 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3ccc(Cl)cc32)CC1 nan
CHEMBL3731783 136020 0 None 331 2 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 459 4 1 3 5.3 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3ccc(Cl)cc32)CC1 nan
44341743 110583 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 418 8 0 4 5.6 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL325430 110583 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 418 8 0 4 5.6 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
44342075 167873 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 360 6 0 2 6.8 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL431076 167873 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 360 6 0 2 6.8 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL2370931 209960 0 None -2 2 Human 7.9 pIC50 = 7.9 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](N)Cc1ccccc1)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)NC1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](CCC(N)=O)NC1=O 10.1021/jm0202122
60155887 77573 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 465 9 0 7 5.0 COc1cc(C)cc(OC)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(OC)nn12 10.1021/jm300259r
CHEMBL2087795 77573 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 465 9 0 7 5.0 COc1cc(C)cc(OC)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(OC)nn12 10.1021/jm300259r
58317445 124413 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 490 6 3 3 6.5 Cc1n[nH]c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1-c1ccccc1 nan
CHEMBL3639509 124413 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 490 6 3 3 6.5 Cc1n[nH]c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1-c1ccccc1 nan
58317390 126533 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 427 4 1 3 5.5 Cc1nn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c(C)c1C nan
CHEMBL3652111 126533 0 None - 1 Human 6.9 pIC50 = 6.9 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 427 4 1 3 5.5 Cc1nn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c(C)c1C nan
59186797 126495 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 401 5 3 4 4.0 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CNc2n[nH]c3c2CCCC3)CC1 nan
CHEMBL3652074 126495 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 401 5 3 4 4.0 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CNc2n[nH]c3c2CCCC3)CC1 nan
58398959 135897 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 466 4 1 5 4.4 Cn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ncccc21 nan
CHEMBL3731041 135897 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 466 4 1 5 4.4 Cn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ncccc21 nan
53341428 136219 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 520 4 1 2 6.4 O=C(N[C@H]1CC[C@H](CN2C(=O)C(F)(F)c3ccc(Cl)cc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3732979 136219 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 520 4 1 2 6.4 O=C(N[C@H]1CC[C@H](CN2C(=O)C(F)(F)c3ccc(Cl)cc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
70696789 76281 0 None - 1 Rat 7.8 pIC50 = 7.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 425 6 0 5 5.9 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(OC(C)C)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058590 76281 0 None - 1 Rat 7.8 pIC50 = 7.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 425 6 0 5 5.9 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(OC(C)C)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
70686397 76294 0 None - 1 Rat 7.8 pIC50 = 7.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 378 5 0 6 4.1 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(OC)nc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058603 76294 0 None - 1 Rat 7.8 pIC50 = 7.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 378 5 0 6 4.1 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(OC)nc3C)ccnc21 10.1016/j.bmcl.2012.06.034
59186799 126511 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 510 6 3 3 6.8 O=C(N[C@H]1CC[C@H](CNc2n[nH]cc2-c2ccc(Cl)cc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652089 126511 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 510 6 3 3 6.8 O=C(N[C@H]1CC[C@H](CNc2n[nH]cc2-c2ccc(Cl)cc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
44342014 9543 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 392 6 0 5 4.7 CCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112290 9543 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 392 6 0 5 4.7 CCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9909978 10038 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Compound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP productionCompound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP production
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
CHEMBL115142 10038 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Compound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP productionCompound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP production
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
21984613 77543 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 389 8 0 4 5.5 CCc1nn2c(-c3ccc(OC)cc3C)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087551 77543 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 389 8 0 4 5.5 CCc1nn2c(-c3ccc(OC)cc3C)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
10385822 76080 0 None - 1 Rat 6.8 pIC50 = 6.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 391 5 0 5 4.7 CC[C@H](COC)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)nccc21 10.1016/j.bmcl.2012.06.034
CHEMBL2057476 76080 0 None - 1 Rat 6.8 pIC50 = 6.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 391 5 0 5 4.7 CC[C@H](COC)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)nccc21 10.1016/j.bmcl.2012.06.034
58317503 126524 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 475 6 2 4 5.8 COc1ncc(Cl)cc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3652102 126524 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 475 6 2 4 5.8 COc1ncc(Cl)cc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
53341600 135369 0 None 30 2 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 439 4 1 3 5.0 Cc1cccc2c1C(C)(C)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(Cl)cnc2C)CC1 nan
CHEMBL3727810 135369 0 None 30 2 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 439 4 1 3 5.0 Cc1cccc2c1C(C)(C)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(Cl)cnc2C)CC1 nan
53341554 135732 0 None 19 2 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 467 4 1 3 5.1 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(F)(F)c3ccc(Cl)cc32)CC1 nan
CHEMBL3730045 135732 0 None 19 2 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 467 4 1 3 5.1 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(F)(F)c3ccc(Cl)cc32)CC1 nan
67185290 126531 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 483 5 2 4 4.4 Cc1cc(N2CCNC2=O)nn1C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3652109 126531 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 483 5 2 4 4.4 Cc1cc(N2CCNC2=O)nn1C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
53341474 136016 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 482 4 1 2 5.9 C[C@]1(F)C(=O)N(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccccc21 nan
CHEMBL3731745 136016 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 482 4 1 2 5.9 C[C@]1(F)C(=O)N(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccccc21 nan
62705998 76077 0 None - 1 Rat 7.8 pIC50 = 7.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 406 6 0 7 3.6 CCC(COC)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ncnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2057473 76077 0 None - 1 Rat 7.8 pIC50 = 7.8 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 406 6 0 7 3.6 CCC(COC)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ncnc21 10.1016/j.bmcl.2012.06.034
44341832 9418 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Compound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP productionCompound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP production
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
CHEMBL111665 9418 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Compound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP productionCompound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP production
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
9952997 170603 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of (Corticotropin-Releasing Factor Receptor) CRF-stimulated cAMP productionInhibition of (Corticotropin-Releasing Factor Receptor) CRF-stimulated cAMP production
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL445075 170603 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of (Corticotropin-Releasing Factor Receptor) CRF-stimulated cAMP productionInhibition of (Corticotropin-Releasing Factor Receptor) CRF-stimulated cAMP production
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
44341832 9418 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL111665 9418 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9908879 10080 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 398 6 0 2 7.1 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL115389 10080 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 398 6 0 2 7.1 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
70696576 75583 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 438 11 0 6 6.1 CCCN(CCC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2046526 75583 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 438 11 0 6 6.1 CCCN(CCC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
70696576 75583 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 438 11 0 6 6.1 CCCN(CCC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2046526 75583 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 438 11 0 6 6.1 CCCN(CCC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
53341472 135391 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 508 5 1 3 6.0 COc1ccc2c(c1)C(C)(C)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3727976 135391 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 508 5 1 3 6.0 COc1ccc2c(c1)C(C)(C)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
60141295 75588 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 410 9 0 6 5.3 CCN(CC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2046534 75588 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 410 9 0 6 5.3 CCN(CC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
58398963 136181 0 None 54 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 459 4 1 3 5.3 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3cccc(Cl)c32)CC1 nan
CHEMBL3732730 136181 0 None 54 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 459 4 1 3 5.3 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3cccc(Cl)c32)CC1 nan
59186812 126500 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 468 5 3 3 5.8 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3cccc(F)c23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652079 126500 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 468 5 3 3 5.8 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3cccc(F)c23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
9821586 168103 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL432800 168103 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
70684375 76613 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 424 9 0 6 4.8 COCCN(C)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063374 76613 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 424 9 0 6 4.8 COCCN(C)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
44816479 126481 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 470 7 2 3 5.8 CN(Cc1cc(-c2ccccc2)n[nH]1)C[C@H]1CC[C@H](NC(=O)c2cc(Cl)ccc2Cl)CC1 nan
CHEMBL3652060 126481 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 470 7 2 3 5.8 CN(Cc1cc(-c2ccccc2)n[nH]1)C[C@H]1CC[C@H](NC(=O)c2cc(Cl)ccc2Cl)CC1 nan
58398949 135319 0 None 109 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 479 5 1 4 5.5 CCn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccccc21 nan
CHEMBL3727515 135319 0 None 109 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 479 5 1 4 5.5 CCn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccccc21 nan
53341019 136240 0 None 16 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 454 6 1 5 4.8 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2c(=O)n(CC(C)C)c3ccccc32)CC1 nan
CHEMBL3733118 136240 0 None 16 2 Human 7.8 pIC50 = 7.8 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 454 6 1 5 4.8 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2c(=O)n(CC(C)C)c3ccccc32)CC1 nan
44341739 113501 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 392 6 1 5 4.5 CCCN(CCO)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL332040 113501 0 None - 1 Human 7.8 pIC50 = 7.8 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 392 6 1 5 4.5 CCCN(CCO)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL2368116 209587 0 None -43 2 Human 7.7 pIC50 = 7.7 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@](C)(CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@](C)(CC(C)C)C(=O)N[C@@H](C(N)=O)[C@H](C)CC)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm0202122
60155989 77577 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 513 11 0 9 4.5 COCc1cc(OC)c(-c2cccc3c(N(CC4CC4)CC4COCCO4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087799 77577 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 513 11 0 9 4.5 COCc1cc(OC)c(-c2cccc3c(N(CC4CC4)CC4COCCO4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
145968888 165158 0 None - 1 Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assay
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc([C@H](OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4228089 165158 0 None - 1 Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assay
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc([C@H](OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
58317267 126535 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 414 4 1 4 4.6 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(C(F)(F)F)cc2C)CC1 nan
CHEMBL3652113 126535 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 414 4 1 4 4.6 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(C(F)(F)F)cc2C)CC1 nan
44587456 188048 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 344 7 0 5 4.7 CCC(CC)Oc1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL497652 188048 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 344 7 0 5 4.7 CCC(CC)Oc1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
44816314 126458 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1ncccc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3652037 126458 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1ncccc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
58317442 126507 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 459 5 2 3 6.1 Cc1ncc(Cl)cc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3652085 126507 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 459 5 2 3 6.1 Cc1ncc(Cl)cc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
59186841 126462 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 508 6 3 3 6.5 C[C@@H]1C[C@@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC[C@@H]1CNc1cc(-c2ccc(F)cc2)[nH]n1 nan
CHEMBL3652041 126462 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 508 6 3 3 6.5 C[C@@H]1C[C@@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC[C@@H]1CNc1cc(-c2ccc(F)cc2)[nH]n1 nan
70696788 76279 0 None - 1 Rat 8.7 pIC50 = 8.7 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 411 6 0 5 5.5 CCOc1cc(Cl)c(-c2ccnc3c2nc(C)c(=O)n3C(CC)C2CC2)cc1C 10.1016/j.bmcl.2012.06.034
CHEMBL2058589 76279 0 None - 1 Rat 8.7 pIC50 = 8.7 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 411 6 0 5 5.5 CCOc1cc(Cl)c(-c2ccnc3c2nc(C)c(=O)n3C(CC)C2CC2)cc1C 10.1016/j.bmcl.2012.06.034
10069877 76082 0 None - 1 Rat 8.7 pIC50 = 8.7 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 405 6 0 6 4.2 CCC(COC)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2057478 76082 0 None - 1 Rat 8.7 pIC50 = 8.7 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 405 6 0 6 4.2 CCC(COC)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
60155709 77554 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 463 9 0 6 5.5 CCc1nn2c(-c3c(OC)cc(C)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087562 77554 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 463 9 0 6 5.5 CCc1nn2c(-c3c(OC)cc(C)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
10200135 77547 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 385 8 0 4 5.9 CCCN(CCC)c1c(CC)nn2c(-c3ccc(OC)cc3Cl)cccc12 10.1021/jm300259r
CHEMBL2087555 77547 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 385 8 0 4 5.9 CCCN(CCC)c1c(CC)nn2c(-c3ccc(OC)cc3Cl)cccc12 10.1021/jm300259r
127035055 135655 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 516 4 1 2 6.5 C[C@@]1(F)C(=O)N(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2cc(Cl)ccc21 nan
CHEMBL3729578 135655 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 516 4 1 2 6.5 C[C@@]1(F)C(=O)N(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2cc(Cl)ccc21 nan
53341116 135809 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 484 4 1 2 5.9 O=C(N[C@H]1CC[C@H](CN2C(=O)Cc3cc(Cl)ccc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3730505 135809 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 484 4 1 2 5.9 O=C(N[C@H]1CC[C@H](CN2C(=O)Cc3cc(Cl)ccc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
10454889 76206 0 None - 1 Rat 7.7 pIC50 = 7.7 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 421 4 0 4 5.8 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(C(F)(F)F)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058334 76206 0 None - 1 Rat 7.7 pIC50 = 7.7 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 421 4 0 4 5.8 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(C(F)(F)F)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
44129684 165030 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assay
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4226158 165030 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assay
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
44815438 126464 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 439 5 2 3 5.8 Cc1cc(C)nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1 nan
CHEMBL3652043 126464 0 None - 1 Human 6.7 pIC50 = 6.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 439 5 2 3 5.8 Cc1cc(C)nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1 nan
71449705 81508 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(OC)c2nc(-c3c(Cl)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160157 81508 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(OC)c2nc(-c3c(Cl)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
58317483 126477 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 413 4 1 3 5.2 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
CHEMBL3652056 126477 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 413 4 1 3 5.2 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
58317373 126505 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 459 5 2 3 6.1 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)ncc1Cl nan
CHEMBL3652083 126505 0 None - 1 Human 7.7 pIC50 = 7.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 459 5 2 3 6.1 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)ncc1Cl nan
44816481 126485 0 None - 1 Human 5.7 pIC50 = 5.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1ccncc1NC[C@H]1CC[C@@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3652064 126485 0 None - 1 Human 5.7 pIC50 = 5.7 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1ccncc1NC[C@H]1CC[C@@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
70690704 76614 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 438 10 0 6 5.2 CCN(CCOC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2063375 76614 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 438 10 0 6 5.2 CCN(CCOC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
10255153 77559 8 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087549 77559 8 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087567 77559 8 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
70690704 76614 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 438 10 0 6 5.2 CCN(CCOC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063375 76614 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 438 10 0 6 5.2 CCN(CCOC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
44816989 126490 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 429 5 2 3 5.3 O=C(N[C@H]1CC[C@H](CNc2ccc(F)cn2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652069 126490 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 429 5 2 3 5.3 O=C(N[C@H]1CC[C@H](CNc2ccc(F)cn2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
58317471 126534 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 461 5 1 3 6.2 O=C(N[C@H]1CC[C@H](Cn2ccc(-c3ccccc3)n2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652112 126534 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 461 5 1 3 6.2 O=C(N[C@H]1CC[C@H](Cn2ccc(-c3ccccc3)n2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
70686532 76611 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 408 8 0 5 5.5 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063372 76611 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 408 8 0 5 5.5 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
62705994 76295 0 None - 1 Rat 7.6 pIC50 = 7.6 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 388 4 0 5 4.8 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ncnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058604 76295 0 None - 1 Rat 7.6 pIC50 = 7.6 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 388 4 0 5 4.8 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ncnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2369694 209648 0 None -4 2 Human 7.6 pIC50 = 7.6 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](N)Cc1ccccc1)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC)NC(=O)[C@@H](C)NC(=O)[C@H](CC(C)C)NC1=O 10.1021/jm0202122
53341430 136232 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 426 4 1 4 4.1 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3cccnc32)CC1 nan
CHEMBL3733081 136232 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 426 4 1 4 4.1 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3cccnc32)CC1 nan
70690481 75905 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 429 6 1 4 6.6 Cc1cc(C)c(Nc2nc3cccc(N(CC4CC4)C4CCOCC4)c3cc2C)c(C)c1 10.1016/j.bmcl.2012.05.066
CHEMBL2049196 75905 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 429 6 1 4 6.6 Cc1cc(C)c(Nc2nc3cccc(N(CC4CC4)C4CCOCC4)c3cc2C)c(C)c1 10.1016/j.bmcl.2012.05.066
71458702 81514 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 462 8 0 5 6.2 CCN(CC)c1ccc(C(F)(F)F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160163 81514 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 462 8 0 5 6.2 CCN(CC)c1ccc(C(F)(F)F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
44816824 126489 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 429 5 2 3 5.3 O=C(N[C@H]1CC[C@H](CNc2cncc(F)c2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652068 126489 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 429 5 2 3 5.3 O=C(N[C@H]1CC[C@H](CNc2cncc(F)c2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL526149 215675 10 None -8 2 Rat 6.6 pIC50 = 6.6 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL None None None CSCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(=O)O)[C@@H](C)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(N)=O 10.1021/jm9000242
53340970 136233 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 427 5 1 6 3.6 CCn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)c2ccncc21 nan
CHEMBL3733082 136233 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 427 5 1 6 3.6 CCn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)c2ccncc21 nan
53341118 135556 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 496 4 1 2 6.1 CC1(C)C(=O)N(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccc(F)cc21 nan
CHEMBL3728921 135556 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 496 4 1 2 6.1 CC1(C)C(=O)N(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccc(F)cc21 nan
71455050 81512 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(Cl)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160161 81512 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(Cl)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
58317277 126493 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 439 6 2 3 5.7 CCc1cncc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1 nan
CHEMBL3652072 126493 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 439 6 2 3 5.7 CCc1cncc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1 nan
58317419 126506 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 464 5 2 4 5.6 Cn1nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccccc21 nan
CHEMBL3652084 126506 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 464 5 2 4 5.6 Cn1nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccccc21 nan
58317366 126517 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 478 6 2 6 4.7 O=C(N[C@H]1CC[C@H](CNc2nnnn2-c2ccccc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652095 126517 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 478 6 2 6 4.7 O=C(N[C@H]1CC[C@H](CNc2nnnn2-c2ccccc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
58317417 126530 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 414 4 1 4 4.6 Cc1nc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
CHEMBL3652108 126530 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 414 4 1 4 4.6 Cc1nc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
70684210 76081 0 None - 1 Rat 8.5 pIC50 = 8.5 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 375 5 0 5 4.4 COc1ccc(-c2ccnc3c2nc(C)c(=O)n3C(C2CC2)C2CC2)c(C)c1 10.1016/j.bmcl.2012.06.034
CHEMBL2057477 76081 0 None - 1 Rat 8.5 pIC50 = 8.5 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 375 5 0 5 4.4 COc1ccc(-c2ccnc3c2nc(C)c(=O)n3C(C2CC2)C2CC2)c(C)c1 10.1016/j.bmcl.2012.06.034
44341723 168133 0 None - 1 Human 8.5 pIC50 = 8.5 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 416 7 0 4 6.3 CCCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL432976 168133 0 None - 1 Human 8.5 pIC50 = 8.5 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 416 7 0 4 6.3 CCCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
70686396 76290 0 None - 1 Rat 8.5 pIC50 = 8.5 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 413 6 0 6 4.8 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(Cl)c(OC)cc3OC)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058599 76290 0 None - 1 Rat 8.5 pIC50 = 8.5 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 413 6 0 6 4.8 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(Cl)c(OC)cc3OC)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2370929 209958 0 None -6 2 Human 8.5 pIC50 = 8.5 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@](C)(CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCNC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@](C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm0202122
10075105 77566 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 511 11 0 8 5.5 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087574 77566 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 511 11 0 8 5.5 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL1794007 208934 0 None 1 2 Human 7.5 pIC50 = 7.5 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](N)Cc1ccccc1)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@H](C)CC)[C@H](C)CC)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC1=O 10.1021/jm0202122
3663 99967 83 None - 1 Human 6.5 pIC50 = 6.5 Functional
Inhibition of recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationInhibition of recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 504 0 6 8 5.1 Cc1cc(O)c2c(=O)c3c(O)cc(O)c4c5c(O)cc(O)c6c(=O)c7c(O)cc(C)c8c1c2c(c34)c(c78)c65 10.1021/np1000329
CHEMBL286494 99967 83 None - 1 Human 6.5 pIC50 = 6.5 Functional
Inhibition of recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationInhibition of recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 504 0 6 8 5.1 Cc1cc(O)c2c(=O)c3c(O)cc(O)c4c5c(O)cc(O)c6c(=O)c7c(O)cc(C)c8c1c2c(c34)c(c78)c65 10.1021/np1000329
58317349 126459 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 412 5 2 5 4.9 Cc1nc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3Cl)CC2)sc1C nan
CHEMBL3652038 126459 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 412 5 2 5 4.9 Cc1nc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3Cl)CC2)sc1C nan
59186870 126492 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 454 5 3 3 5.4 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3c2CCCC3)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652071 126492 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 454 5 3 3 5.4 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3c2CCCC3)CC1)c1cc(C(F)(F)F)ccc1Cl nan
71458705 81521 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 438 10 0 6 5.5 CCc1cc2c(N(CC)CC)ccc(OC)c2nc1-c1c(OC)cc(COC)cc1OC 10.1016/j.bmc.2012.09.028
CHEMBL2160170 81521 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 438 10 0 6 5.5 CCc1cc2c(N(CC)CC)ccc(OC)c2nc1-c1c(OC)cc(COC)cc1OC 10.1016/j.bmc.2012.09.028
59186828 126504 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 480 6 3 4 5.6 COc1ccc2c(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)n[nH]c2c1 nan
CHEMBL3652082 126504 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 480 6 3 4 5.6 COc1ccc2c(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)n[nH]c2c1 nan
44815273 126484 0 None - 1 Human 5.5 pIC50 = 5.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 494 6 3 3 6.3 O=C(N[C@H]1CC[C@@H](CNc2cc(-c3ccc(F)cc3)n[nH]2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652063 126484 0 None - 1 Human 5.5 pIC50 = 5.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 494 6 3 3 6.3 O=C(N[C@H]1CC[C@@H](CNc2cc(-c3ccc(F)cc3)n[nH]2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
71458704 81517 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 410 9 0 6 4.9 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmc.2012.09.028
CHEMBL2160167 81517 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 410 9 0 6 4.9 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmc.2012.09.028
58317316 126529 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 435 4 1 3 5.7 O=C(N[C@H]1CC[C@H](Cn2cc3ccccc3n2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652107 126529 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 435 4 1 3 5.7 O=C(N[C@H]1CC[C@H](Cn2cc3ccccc3n2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
58317324 126525 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 448 5 3 3 5.4 Cc1n[nH]c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1Cl nan
CHEMBL3652103 126525 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 448 5 3 3 5.4 Cc1n[nH]c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1Cl nan
70692691 76205 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 375 4 0 4 5.4 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(C)c(C)c3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058333 76205 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 375 4 0 4 5.4 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(C)c(C)c3C)ccnc21 10.1016/j.bmcl.2012.06.034
44815603 126468 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 491 7 2 4 6.1 O=C(N[C@H]1CC[C@H](CNCc2cc(-c3ccccc3)on2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652047 126468 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 491 7 2 4 6.1 O=C(N[C@H]1CC[C@H](CNCc2cc(-c3ccccc3)on2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
53341473 135564 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 509 5 1 4 5.4 COc1cc2c(cn1)C(C)(C)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3729005 135564 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 509 5 1 4 5.4 COc1cc2c(cn1)C(C)(C)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
53357410 126538 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 360 4 1 4 3.8 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
CHEMBL3652116 126538 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 360 4 1 4 3.8 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
9906984 76183 0 None - 1 Rat 5.5 pIC50 = 5.5 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 361 3 0 4 4.7 Cc1nc2c(-c3ccc(Cl)cc3Cl)ccnc2n(CC(C)C)c1=O 10.1016/j.bmcl.2012.06.034
CHEMBL2058066 76183 0 None - 1 Rat 5.5 pIC50 = 5.5 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 361 3 0 4 4.7 Cc1nc2c(-c3ccc(Cl)cc3Cl)ccnc2n(CC(C)C)c1=O 10.1016/j.bmcl.2012.06.034
42618197 184306 0 None -5 2 Rat 7.4 pIC50 = 7.4 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 391 6 1 6 4.8 CCC(CC)Nc1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
CHEMBL484158 184306 0 None -5 2 Rat 7.4 pIC50 = 7.4 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 391 6 1 6 4.8 CCC(CC)Nc1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
71458703 81515 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 419 8 0 6 5.1 CCN(CC)c1ccc(C#N)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160164 81515 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 419 8 0 6 5.1 CCN(CC)c1ccc(C#N)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
44815437 126463 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 431 5 2 4 5.5 Cc1cnc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)s1 nan
CHEMBL3652042 126463 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 431 5 2 4 5.5 Cc1cnc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)s1 nan
12086065 10835 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 406 7 0 5 5.1 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL117209 10835 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 406 7 0 5 5.1 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9908466 114804 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Compound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP productionCompound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP production
ChEMBL 390 6 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL334039 114804 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Compound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP productionCompound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP production
ChEMBL 390 6 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
53341173 135307 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 465 4 1 4 5.0 Cn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccccc21 nan
CHEMBL3727446 135307 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 465 4 1 4 5.0 Cn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c2ccccc21 nan
62705997 76076 0 None - 1 Rat 7.4 pIC50 = 7.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 376 5 0 6 3.8 COc1ccc(-c2ncnc3c2nc(C)c(=O)n3C(C2CC2)C2CC2)c(C)c1 10.1016/j.bmcl.2012.06.034
CHEMBL2057472 76076 0 None - 1 Rat 7.4 pIC50 = 7.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 376 5 0 6 3.8 COc1ccc(-c2ncnc3c2nc(C)c(=O)n3C(C2CC2)C2CC2)c(C)c1 10.1016/j.bmcl.2012.06.034
59186851 126510 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 490 6 3 3 6.5 Cc1c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n[nH]c1-c1ccccc1 nan
CHEMBL3652088 126510 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 490 6 3 3 6.5 Cc1c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n[nH]c1-c1ccccc1 nan
59186801 126520 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 477 6 3 4 5.5 O=C(N[C@H]1CC[C@H](CNc2[nH]ncc2-c2cccnc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652098 126520 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 477 6 3 4 5.5 O=C(N[C@H]1CC[C@H](CNc2[nH]ncc2-c2cccnc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
70688432 75902 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 375 7 1 3 6.8 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2049193 75902 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 375 7 1 3 6.8 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)cc12 10.1016/j.bmcl.2012.05.066
70696935 76609 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 450 11 0 5 6.6 CCCN(CCC)c1ccc(CC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063370 76609 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 450 11 0 5 6.6 CCCN(CCC)c1ccc(CC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
53341596 135662 0 None 79 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 455 5 1 4 4.7 COc1ccc2c(c1)N(C[C@H]1CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC1)C(=O)C2(C)C nan
CHEMBL3729602 135662 0 None 79 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 455 5 1 4 4.7 COc1ccc2c(c1)N(C[C@H]1CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC1)C(=O)C2(C)C nan
42618195 184286 0 None 1 2 Rat 7.4 pIC50 = 7.4 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 413 9 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c(-c3cc(C)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL483993 184286 0 None 1 2 Rat 7.4 pIC50 = 7.4 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 413 9 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c(-c3cc(C)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
62705996 76297 0 None - 1 Rat 7.4 pIC50 = 7.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 434 6 0 6 5.1 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(Cl)c(OC(F)F)cc3C)ncnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058606 76297 0 None - 1 Rat 7.4 pIC50 = 7.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 434 6 0 6 5.1 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(Cl)c(OC(F)F)cc3C)ncnc21 10.1016/j.bmcl.2012.06.034
44814573 126457 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1cccnc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3652036 126457 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1cccnc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
58317295 126512 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 406 5 2 4 4.8 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)ncc1Cl nan
CHEMBL3652090 126512 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 406 5 2 4 4.8 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)ncc1Cl nan
44341814 110664 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 422 8 0 6 4.4 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL325918 110664 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 422 8 0 6 4.4 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
22052143 76184 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 375 3 0 4 5.3 Cc1nc2c(-c3ccc(Cl)cc3Cl)ccnc2n(C(C)C(C)C)c1=O 10.1016/j.bmcl.2012.06.034
CHEMBL2058067 76184 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 375 3 0 4 5.3 Cc1nc2c(-c3ccc(Cl)cc3Cl)ccnc2n(C(C)C(C)C)c1=O 10.1016/j.bmcl.2012.06.034
70682294 76617 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 394 8 0 5 5.2 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmc.2012.09.028
CHEMBL2063380 76617 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 394 8 0 5 5.2 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmc.2012.09.028
70682294 76617 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 394 8 0 5 5.2 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063380 76617 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 394 8 0 5 5.2 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmcl.2012.07.047
60155888 77574 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 481 9 0 7 5.7 COc1cc(C)cc(OC)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(SC)nn12 10.1021/jm300259r
CHEMBL2087796 77574 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 481 9 0 7 5.7 COc1cc(C)cc(OC)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(SC)nn12 10.1021/jm300259r
59186815 126466 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1cccc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
CHEMBL3652045 126466 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1cccc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
3520 3267 54 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassayAntagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassay
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm300864p
9821250 3267 54 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassayAntagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassay
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm300864p
CHEMBL309138 3267 54 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassayAntagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassay
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm300864p
9977800 76200 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 391 5 0 5 4.7 CC[C@H](COC)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058329 76200 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 391 5 0 5 4.7 CC[C@H](COC)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
10339953 76208 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 383 5 0 5 4.8 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058336 76208 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 383 5 0 5 4.8 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
22052073 76198 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 401 5 0 4 5.8 CCCC(C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058327 76198 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 401 5 0 4 5.8 CCCC(C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
57786006 164963 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assay
ChEMBL 422 4 0 4 6.4 CCN(CC)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4225254 164963 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assay
ChEMBL 422 4 0 4 6.4 CCN(CC)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
10362573 76209 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 383 5 0 5 4.8 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058337 76209 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 383 5 0 5 4.8 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
70694746 76282 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 397 5 0 5 5.1 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(Cl)c(OC)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058591 76282 0 None - 1 Rat 8.4 pIC50 = 8.4 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 397 5 0 5 5.1 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(Cl)c(OC)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
70682138 76288 0 None - 1 Rat 8.3 pIC50 = 8.3 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 392 4 0 5 5.0 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C#N)c(C)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058597 76288 0 None - 1 Rat 8.3 pIC50 = 8.3 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 392 4 0 5 5.0 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C#N)c(C)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
44194975 196310 16 None -4 2 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at CRF1 receptor in human Y-79 cells assessed as inhibition of CRF-induced cAMP production after 30 mins by HTRF analysisAntagonist activity at CRF1 receptor in human Y-79 cells assessed as inhibition of CRF-induced cAMP production after 30 mins by HTRF analysis
ChEMBL 423 6 1 5 5.5 C[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL562219 196310 16 None -4 2 Human 8.3 pIC50 = 8.3 Functional
Antagonist activity at CRF1 receptor in human Y-79 cells assessed as inhibition of CRF-induced cAMP production after 30 mins by HTRF analysisAntagonist activity at CRF1 receptor in human Y-79 cells assessed as inhibition of CRF-induced cAMP production after 30 mins by HTRF analysis
ChEMBL 423 6 1 5 5.5 C[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1021/jm900302q
44816316 126480 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1cncc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1 nan
CHEMBL3652059 126480 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1cncc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1 nan
53340971 135346 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 427 4 1 6 3.4 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2c(=O)n(C)c3nccc(C)c32)CC1 nan
CHEMBL3727694 135346 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 427 4 1 6 3.4 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2c(=O)n(C)c3nccc(C)c32)CC1 nan
71456848 81510 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 394 7 0 5 5.4 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(C)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160159 81510 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 394 7 0 5 5.4 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(C)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
59186833 126527 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 442 6 3 3 5.4 CCc1[nH]nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1C nan
CHEMBL3652105 126527 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 442 6 3 3 5.4 CCc1[nH]nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1C nan
53340926 135775 0 None 19 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 463 4 1 3 5.2 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(F)c3ccc(Cl)cc32)CC1 nan
CHEMBL3730298 135775 0 None 19 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 463 4 1 3 5.2 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(F)c3ccc(Cl)cc32)CC1 nan
53341018 135944 0 None 5 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 426 5 1 5 4.2 CCn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)c2ccccc21 nan
CHEMBL3731280 135944 0 None 5 2 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 426 5 1 5 4.2 CCn1c(=O)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)c2ccccc21 nan
11948286 156669 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulationAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation
ChEMBL 410 5 0 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4069551 156669 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulationAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation
ChEMBL 410 5 0 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
70684376 76619 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2063382 76619 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmc.2012.09.028
70684376 76619 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063382 76619 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2370917 209952 0 None -34 2 Human 7.4 pIC50 = 7.4 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@](C)(CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@](C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm0202122
70692846 76612 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 460 10 0 5 6.3 COCc1cc(OC)c(-c2nc3c(C)ccc(N(CC4CC4)CC4CC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
CHEMBL2063373 76612 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 460 10 0 5 6.3 COCc1cc(OC)c(-c2nc3c(C)ccc(N(CC4CC4)CC4CC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
70692631 75900 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 378 7 2 4 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)[nH]c12 10.1016/j.bmcl.2012.05.066
CHEMBL2049190 75900 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 378 7 2 4 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)[nH]c12 10.1016/j.bmcl.2012.05.066
53341117 136107 0 None 83 2 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 468 4 1 2 5.4 O=C(N[C@H]1CC[C@H](CN2C(=O)Cc3ccc(F)cc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3732322 136107 0 None 83 2 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 468 4 1 2 5.4 O=C(N[C@H]1CC[C@H](CN2C(=O)Cc3ccc(F)cc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
44815110 126478 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 440 6 3 3 5.4 O=C(N[C@H]1CC[C@H](CNc2cc(C3CC3)n[nH]2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652057 126478 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 440 6 3 3 5.4 O=C(N[C@H]1CC[C@H](CNc2cc(C3CC3)n[nH]2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
53341427 135344 0 None 79 2 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 425 4 1 3 4.7 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3ccccc32)CC1 nan
CHEMBL3727689 135344 0 None 79 2 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 425 4 1 3 4.7 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3ccccc32)CC1 nan
21984746 77548 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 365 8 0 4 5.5 CCCN(CCC)c1c(CC)nn2c(-c3ccc(OC)cc3C)cccc12 10.1021/jm300259r
CHEMBL2087556 77548 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 365 8 0 4 5.5 CCCN(CCC)c1c(CC)nn2c(-c3ccc(OC)cc3C)cccc12 10.1021/jm300259r
9952997 170603 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
Compound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP productionCompound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP production
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
CHEMBL445075 170603 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
Compound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP productionCompound was tested to inhibit Corticotropin releasing factor receptor 1-stimulated c-AMP production
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
9909978 10038 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL115142 10038 0 None - 1 Human 8.3 pIC50 = 8.3 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
70696779 76204 0 None - 1 Rat 8.3 pIC50 = 8.3 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 361 4 0 4 5.1 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(C)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058332 76204 0 None - 1 Rat 8.3 pIC50 = 8.3 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 361 4 0 4 5.1 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(C)c(C)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2370933 209961 0 None -9 2 Human 8.2 pIC50 = 8.2 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@](C)(CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NC(CC(=O)O)C(=O)N[C@@](C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC1=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm0202122
53341556 135595 0 None 33 2 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 508 5 1 3 6.0 COc1cccc2c1N(C[C@H]1CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC1)C(=O)C2(C)C nan
CHEMBL3729197 135595 0 None 33 2 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 508 5 1 3 6.0 COc1cccc2c1N(C[C@H]1CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC1)C(=O)C2(C)C nan
58801647 77567 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 479 10 0 7 5.1 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087575 77567 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 479 10 0 7 5.1 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 10.1021/jm300259r
59186865 126474 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 410 5 2 2 5.8 O=C(N[C@H]1CC[C@H](CNc2ccccc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652053 126474 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 410 5 2 2 5.8 O=C(N[C@H]1CC[C@H](CNc2ccccc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
44815774 126479 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 428 5 2 2 5.9 O=C(N[C@H]1CC[C@H](CNc2cccc(F)c2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652058 126479 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 428 5 2 2 5.9 O=C(N[C@H]1CC[C@H](CNc2cccc(F)c2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
3520 3267 54 None - 1 Human 7.3 pIC50 = 7.3 Functional
Inhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptorInhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm050384+
9821250 3267 54 None - 1 Human 7.3 pIC50 = 7.3 Functional
Inhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptorInhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm050384+
CHEMBL309138 3267 54 None - 1 Human 7.3 pIC50 = 7.3 Functional
Inhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptorInhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm050384+
59186804 126487 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 424 5 2 2 6.0 C[C@H]1CC(CNc2ccccc2)CCC1NC(=O)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652066 126487 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 424 5 2 2 6.0 C[C@H]1CC(CNc2ccccc2)CCC1NC(=O)c1cc(C(F)(F)F)ccc1Cl nan
44341636 9695 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 386 6 0 2 7.1 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL113097 9695 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Inhibition of Corticotropin releasing factor receptor 1-stimulated cAMP productionInhibition of Corticotropin releasing factor receptor 1-stimulated cAMP production
ChEMBL 386 6 0 2 7.1 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
60155540 77572 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 490 10 0 8 4.7 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(C#N)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087794 77572 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 490 10 0 8 4.7 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(C#N)nn23)c(OC)c1 10.1021/jm300259r
70688490 76286 0 None - 1 Rat 7.3 pIC50 = 7.3 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 385 5 0 5 4.4 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3F)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058595 76286 0 None - 1 Rat 7.3 pIC50 = 7.3 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 385 5 0 5 4.4 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3F)ccnc21 10.1016/j.bmcl.2012.06.034
58317486 126516 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 475 6 2 4 5.8 COc1ccc(Cl)c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
CHEMBL3652094 126516 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 475 6 2 4 5.8 COc1ccc(Cl)c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
59186805 126502 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 464 5 3 3 5.9 Cc1cccc2[nH]nc(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)c12 nan
CHEMBL3652080 126502 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 464 5 3 3 5.9 Cc1cccc2[nH]nc(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)c12 nan
59186875 126508 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 465 5 3 4 5.3 Cc1ccc2c(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)n[nH]c2n1 nan
CHEMBL3652086 126508 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 465 5 3 4 5.3 Cc1ccc2c(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)n[nH]c2n1 nan
58317325 126536 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 459 5 2 3 6.1 Cc1ncc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)cc1Cl nan
CHEMBL3652114 126536 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 459 5 2 3 6.1 Cc1ncc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)cc1Cl nan
145969226 164997 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assay
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc([C@@H](OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4225709 164997 0 None - 1 Human 7.3 pIC50 = 7.3 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of human CRF-stimulated cAMP accumulation after 4 hrs by luciferase reporter gene assay
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc([C@@H](OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
11740957 76079 0 None - 1 Rat 7.3 pIC50 = 7.3 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 387 4 0 4 5.4 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)nccc21 10.1016/j.bmcl.2012.06.034
CHEMBL2057475 76079 0 None - 1 Rat 7.3 pIC50 = 7.3 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 387 4 0 4 5.4 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)nccc21 10.1016/j.bmcl.2012.06.034
70692630 75898 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 376 7 1 4 6.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.bmcl.2012.05.066
CHEMBL2049188 75898 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation preincubated for 30 mins measured after 30 mins by enzyme immunoassay
ChEMBL 376 7 1 4 6.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.bmcl.2012.05.066
53341597 135296 0 None 37 2 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 492 4 1 2 6.3 Cc1cccc2c1N(C[C@H]1CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC1)C(=O)C2(C)C nan
CHEMBL3727391 135296 0 None 37 2 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 492 4 1 2 6.3 Cc1cccc2c1N(C[C@H]1CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC1)C(=O)C2(C)C nan
71453344 81519 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 444 9 0 6 5.6 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160169 81519 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 444 9 0 6 5.6 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmc.2012.09.028
59186854 126513 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 524 6 3 3 7.1 Cc1[nH]nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1-c1ccc(Cl)cc1 nan
CHEMBL3652091 126513 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 524 6 3 3 7.1 Cc1[nH]nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1-c1ccc(Cl)cc1 nan
53358726 126488 0 None - 1 Human 6.2 pIC50 = 6.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 374 4 1 4 4.2 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(C)c(C)c2C)CC1 nan
CHEMBL3652067 126488 0 None - 1 Human 6.2 pIC50 = 6.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 374 4 1 4 4.2 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(C)c(C)c2C)CC1 nan
53341068 136123 0 None 77 2 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 457 4 1 3 5.2 Cc1cc2c(cc1C)C(C)(F)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(Cl)cnc2C)CC1 nan
CHEMBL3732415 136123 0 None 77 2 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 457 4 1 3 5.2 Cc1cc2c(cc1C)C(C)(F)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(Cl)cnc2C)CC1 nan
21984771 77545 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 403 8 0 4 5.8 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087553 77545 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 403 8 0 4 5.8 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
59186844 126515 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 476 6 3 3 6.2 O=C(N[C@H]1CC[C@H](CNc2n[nH]cc2-c2ccccc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652093 126515 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 476 6 3 3 6.2 O=C(N[C@H]1CC[C@H](CNc2n[nH]cc2-c2ccccc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
58317306 126526 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 524 6 2 4 6.9 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n(-c2ccc(Cl)cc2)n1 nan
CHEMBL3652104 126526 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 524 6 2 4 6.9 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n(-c2ccc(Cl)cc2)n1 nan
53341068 136123 0 None 77 2 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 457 4 1 3 5.2 Cc1cc2c(cc1C)C(C)(F)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(Cl)cnc2C)CC1 nan
CHEMBL3732415 136123 0 None 77 2 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 457 4 1 3 5.2 Cc1cc2c(cc1C)C(C)(F)C(=O)N2C[C@H]1CC[C@H](NC(=O)c2cc(Cl)cnc2C)CC1 nan
59186847 126469 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 445 5 2 4 5.8 Cc1nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)sc1C nan
CHEMBL3652048 126469 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 445 5 2 4 5.8 Cc1nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)sc1C nan
44815273 126470 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 494 6 3 3 6.3 O=C(N[C@H]1CC[C@H](CNc2cc(-c3ccc(F)cc3)n[nH]2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652049 126470 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 494 6 3 3 6.3 O=C(N[C@H]1CC[C@H](CNc2cc(-c3ccc(F)cc3)n[nH]2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
59186813 126471 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 442 7 3 3 5.4 CCCc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n[nH]1 nan
CHEMBL3652050 126471 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 442 7 3 3 5.4 CCCc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n[nH]1 nan
53341066 135601 0 None - 1 Human 6.2 pIC50 = 6.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 459 4 1 3 5.0 Cc1ncc(C(F)(F)F)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3ccccc32)CC1 nan
CHEMBL3729224 135601 0 None - 1 Human 6.2 pIC50 = 6.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 459 4 1 3 5.0 Cc1ncc(C(F)(F)F)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)C(C)(C)c3ccccc32)CC1 nan
53341558 136115 0 None 74 2 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 429 4 1 3 4.6 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)[C@@](C)(F)c3ccccc32)CC1 nan
CHEMBL3732369 136115 0 None 74 2 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 429 4 1 3 4.6 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CN2C(=O)[C@@](C)(F)c3ccccc32)CC1 nan
22052205 76185 0 None - 1 Rat 7.2 pIC50 = 7.2 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 375 4 0 4 5.4 CCCC(C)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058068 76185 0 None - 1 Rat 7.2 pIC50 = 7.2 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 375 4 0 4 5.4 CCCC(C)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
59186819 126494 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 390 5 2 4 4.3 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)ncc1F nan
CHEMBL3652073 126494 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 390 5 2 4 4.3 Cc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)ncc1F nan
59186796 126503 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 484 5 3 3 6.3 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3ccc(Cl)cc23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652081 126503 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 484 5 3 3 6.3 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3ccc(Cl)cc23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
71451515 81509 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 405 7 0 6 5.0 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(C#N)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160158 81509 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 405 7 0 6 5.0 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(C#N)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
22052069 76199 0 None - 1 Rat 7.2 pIC50 = 7.2 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 377 4 0 5 4.3 COCC(C)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058328 76199 0 None - 1 Rat 7.2 pIC50 = 7.2 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 377 4 0 5 4.3 COCC(C)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
59186871 126467 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 444 5 2 2 6.4 O=C(N[C@H]1CC[C@H](CNc2ccccc2Cl)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652046 126467 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 444 5 2 2 6.4 O=C(N[C@H]1CC[C@H](CNc2ccccc2Cl)CC1)c1cc(C(F)(F)F)ccc1Cl nan
44815276 126472 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 442 6 3 3 5.6 CC(C)c1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n[nH]1 nan
CHEMBL3652051 126472 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 442 6 3 3 5.6 CC(C)c1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n[nH]1 nan
67238091 126460 0 None - 1 Human 5.2 pIC50 = 5.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 455 6 3 4 4.9 O=C(O)c1ccc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)nc1 nan
CHEMBL3652039 126460 0 None - 1 Human 5.2 pIC50 = 5.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 455 6 3 4 4.9 O=C(O)c1ccc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)nc1 nan
53341425 135952 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 484 4 1 2 5.9 O=C(N[C@H]1CC[C@H](CN2C(=O)Cc3ccc(Cl)cc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3731360 135952 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 484 4 1 2 5.9 O=C(N[C@H]1CC[C@H](CN2C(=O)Cc3ccc(Cl)cc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
71455053 81524 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 482 12 0 7 5.5 COCCN(CC(C)C)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160173 81524 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 482 12 0 7 5.5 COCCN(CC(C)C)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
9908904 180487 4 None -5 2 Rat 7.2 pIC50 = 7.2 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL474287 180487 4 None -5 2 Rat 7.2 pIC50 = 7.2 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL475306 180487 4 None -5 2 Rat 7.2 pIC50 = 7.2 Functional
Antagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP productionAntagonist activity at CRF1 receptor in rat brain homogenates assessed as inhibition of CRF-stimulted cAMP production
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
44815440 126465 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1ccc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)nc1 nan
CHEMBL3652044 126465 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 425 5 2 3 5.5 Cc1ccc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)nc1 nan
58317463 126475 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 392 5 2 5 4.5 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CNc2nc(C)c(C)s2)CC1 nan
CHEMBL3652054 126475 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 392 5 2 5 4.5 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CNc2nc(C)c(C)s2)CC1 nan
71453343 81511 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160160 81511 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
59186843 126514 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 451 5 3 4 5.0 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3cccnc23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652092 126514 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 451 5 3 4 5.0 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3cccnc23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
58317395 126518 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 490 6 2 4 6.2 Cn1cc(-c2ccccc2)c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
CHEMBL3652096 126518 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 490 6 2 4 6.2 Cn1cc(-c2ccccc2)c(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
24971237 188049 0 None - 1 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 380 8 0 6 4.7 CCC(CC)Oc1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL497653 188049 0 None - 1 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 380 8 0 6 4.7 CCC(CC)Oc1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
57912459 82617 5 None - 1 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassayAntagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassay
ChEMBL 503 12 0 9 5.4 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179195 82617 5 None - 1 Human 8.2 pIC50 = 8.2 Functional
Antagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassayAntagonist activity at CRF1 receptor in human IMR32 cells assessed as inhibition of CRF-induced intracellular cAMP accumulation after 30 mins by immunoassay
ChEMBL 503 12 0 9 5.4 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
69658040 76207 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 419 6 0 5 5.4 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC(F)F)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058335 76207 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 419 6 0 5 5.4 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC(F)F)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
10249650 76197 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 387 4 0 4 5.4 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058326 76197 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 387 4 0 4 5.4 CC[C@@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
62706160 76078 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 418 6 0 7 3.6 COCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ncnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2057474 76078 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 418 6 0 7 3.6 COCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3Cl)ncnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2370916 209951 0 None -13 2 Human 8.1 pIC50 = 8.1 Functional
Inhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagineInhibition of recombinant corticotropin releasing factor receptor 1 assayed using nonselective [125I]-labeled agonist [Tyr0,Glu1,Nle17]-sauvagine
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H](N)CCC(=O)O)[C@@H](C)CC)[C@@H](C)CC)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N(C)[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)O)NC(=O)[C@@H](C)NC(=O)[C@H](CCC(N)=O)NC1=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm0202122
70682293 76608 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 436 10 0 5 6.3 CCCN(CCC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2063369 76608 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 436 10 0 5 6.3 CCCN(CCC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
70682293 76608 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 436 10 0 5 6.3 CCCN(CCC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063369 76608 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 436 10 0 5 6.3 CCCN(CCC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
58317340 126483 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 427 5 2 3 5.7 O=C(N[C@H]1CC[C@H](CNc2cccc3ncccc23)CC1)c1cccc(C(F)(F)F)c1 nan
CHEMBL3652062 126483 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 427 5 2 3 5.7 O=C(N[C@H]1CC[C@H](CNc2cccc3ncccc23)CC1)c1cccc(C(F)(F)F)c1 nan
58317279 126537 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 394 4 1 4 4.5 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(C)c(Cl)c2C)CC1 nan
CHEMBL3652115 126537 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 394 4 1 4 4.5 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(C)c(Cl)c2C)CC1 nan
9843598 67776 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Inhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptorInhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptor
ChEMBL 394 7 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL190845 67776 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Inhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptorInhibition of CRF stimulated cAMP production in CHO cells expressing CRF1 receptor
ChEMBL 394 7 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
58317422 126522 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 376 5 2 4 4.0 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CNc2ccc(F)cn2)CC1 nan
CHEMBL3652100 126522 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 376 5 2 4 4.0 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](CNc2ccc(F)cn2)CC1 nan
9908904 180487 4 None -5 2 Rat 7.1 pIC50 = 7.1 Functional
Agonist activity at CRF1 receptor in rat pituitary cellsAgonist activity at CRF1 receptor in rat pituitary cells
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm900025h
CHEMBL474287 180487 4 None -5 2 Rat 7.1 pIC50 = 7.1 Functional
Agonist activity at CRF1 receptor in rat pituitary cellsAgonist activity at CRF1 receptor in rat pituitary cells
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm900025h
CHEMBL475306 180487 4 None -5 2 Rat 7.1 pIC50 = 7.1 Functional
Agonist activity at CRF1 receptor in rat pituitary cellsAgonist activity at CRF1 receptor in rat pituitary cells
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm900025h
10363079 76202 0 None - 1 Rat 7.1 pIC50 = 7.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 391 5 0 5 4.7 CC[C@@H](COC)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058330 76202 0 None - 1 Rat 7.1 pIC50 = 7.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 391 5 0 5 4.7 CC[C@@H](COC)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
71455052 81518 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 428 9 0 6 5.1 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160168 81518 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 428 9 0 6 5.1 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmc.2012.09.028
9865624 15544 12 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptorAntagonist activity at human CRF1 receptor
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmc.2022.116614
CHEMBL121896 15544 12 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptorAntagonist activity at human CRF1 receptor
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmc.2022.116614
11774042 203352 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptorAntagonist activity at human CRF1 receptor
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmc.2022.116614
CHEMBL65078 203352 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptorAntagonist activity at human CRF1 receptor
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmc.2022.116614
10338811 76292 0 None - 1 Rat 7.1 pIC50 = 7.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 364 5 0 6 3.8 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC)nc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058601 76292 0 None - 1 Rat 7.1 pIC50 = 7.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 364 5 0 6 3.8 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(OC)nc3C)ccnc21 10.1016/j.bmcl.2012.06.034
44815112 126473 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 411 5 2 3 5.2 O=C(N[C@H]1CC[C@H](CNc2cccnc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652052 126473 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 411 5 2 3 5.2 O=C(N[C@H]1CC[C@H](CNc2cccnc2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
59186853 126519 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 429 5 2 4 5.4 Cc1noc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1C nan
CHEMBL3652097 126519 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 429 5 2 4 5.4 Cc1noc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1C nan
59186802 126509 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 520 7 3 3 6.2 CCCc1[nH]nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1Br nan
CHEMBL3652087 126509 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 520 7 3 3 6.2 CCCc1[nH]nc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1Br nan
11025 2740 7 None - 1 Human 7.1 pIC50 = 7.1 Functional
In vitro inhibition of CRF-stimulated cAMP production in cell membranes expressing human CRF1 receptorIn vitro inhibition of CRF-stimulated cAMP production in cell membranes expressing human CRF1 receptor
ChEMBL 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 10.1021/jm049085v
11713007 2740 7 None - 1 Human 7.1 pIC50 = 7.1 Functional
In vitro inhibition of CRF-stimulated cAMP production in cell membranes expressing human CRF1 receptorIn vitro inhibition of CRF-stimulated cAMP production in cell membranes expressing human CRF1 receptor
ChEMBL 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 10.1021/jm049085v
CHEMBL380800 2740 7 None - 1 Human 7.1 pIC50 = 7.1 Functional
In vitro inhibition of CRF-stimulated cAMP production in cell membranes expressing human CRF1 receptorIn vitro inhibition of CRF-stimulated cAMP production in cell membranes expressing human CRF1 receptor
ChEMBL 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 10.1021/jm049085v
10407938 76186 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 387 4 0 4 5.4 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058069 76186 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 387 4 0 4 5.4 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ccnc21 10.1016/j.bmcl.2012.06.034
70692690 76203 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 347 4 0 4 4.7 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3ccc(C)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058331 76203 0 None - 1 Rat 8.1 pIC50 = 8.1 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 347 4 0 4 4.7 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3ccc(C)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
58317325 126536 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 459 5 2 3 6.1 Cc1ncc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)cc1Cl nan
CHEMBL3652114 126536 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 459 5 2 3 6.1 Cc1ncc(NC[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)cc1Cl nan
58317360 126496 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 455 6 2 4 5.5 COc1ncc(C)cc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3652075 126496 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 455 6 2 4 5.5 COc1ncc(C)cc1NC[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
53341022 136179 0 None 41 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 412 4 1 5 3.7 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2c(=O)n(C)c3ccccc32)CC1 nan
CHEMBL3732721 136179 0 None 41 2 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 412 4 1 5 3.7 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2c(=O)n(C)c3ccccc32)CC1 nan
59186825 126498 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 464 5 3 3 5.9 Cc1ccc2[nH]nc(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)c2c1 nan
CHEMBL3652077 126498 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 464 5 3 3 5.9 Cc1ccc2[nH]nc(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)c2c1 nan
70909805 139314 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-stimulated cAMP accumulation after 4 hrs by steady-glo luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-stimulated cAMP accumulation after 4 hrs by steady-glo luciferase reporter gene assay
ChEMBL 434 8 1 5 6.6 CCCN(CCC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3792517 139314 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-stimulated cAMP accumulation after 4 hrs by steady-glo luciferase reporter gene assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-stimulated cAMP accumulation after 4 hrs by steady-glo luciferase reporter gene assay
ChEMBL 434 8 1 5 6.6 CCCN(CCC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
59186817 126497 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 451 5 3 4 5.0 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3ncccc23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652076 126497 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 451 5 3 4 5.0 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3ncccc23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
53341471 135585 0 None - 1 Human 8.1 pIC50 = 8.1 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 494 4 1 2 5.9 O=C(N[C@H]1CC[C@H](CN2C(=O)C3(CC3)c3cc(F)ccc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3729128 135585 0 None - 1 Human 8.1 pIC50 = 8.1 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 494 4 1 2 5.9 O=C(N[C@H]1CC[C@H](CN2C(=O)C3(CC3)c3cc(F)ccc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
10429933 76285 0 None - 1 Rat 8.0 pIC50 = 8.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 381 5 0 5 4.6 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058594 76285 0 None - 1 Rat 8.0 pIC50 = 8.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 381 5 0 5 4.6 CC[C@H](C1CC1)n1c(=O)c(C)nc2c(-c3cc(F)c(OC)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
70692700 76283 0 None - 1 Rat 8.0 pIC50 = 8.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 433 6 0 5 5.7 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(Cl)c(OC(F)F)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058592 76283 0 None - 1 Rat 8.0 pIC50 = 8.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 433 6 0 5 5.7 CCC(C1CC1)n1c(=O)c(C)nc2c(-c3cc(Cl)c(OC(F)F)cc3C)ccnc21 10.1016/j.bmcl.2012.06.034
21984718 77546 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 403 8 0 4 5.8 CCc1nn2c(-c3c(C)cc(OC)cc3C)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087554 77546 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysisAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated cAMP accumulation after 30 mins by fluorescence analysis
ChEMBL 403 8 0 4 5.8 CCc1nn2c(-c3c(C)cc(OC)cc3C)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
44816141 126476 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 469 5 2 4 4.1 O=C(N[C@H]1CC[C@H](Cn2ccc(N3CCNC3=O)n2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652055 126476 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 469 5 2 4 4.1 O=C(N[C@H]1CC[C@H](Cn2ccc(N3CCNC3=O)n2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
59186860 126499 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 468 5 3 3 5.8 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3ccc(F)cc23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3652078 126499 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 468 5 3 3 5.8 O=C(N[C@H]1CC[C@H](CNc2n[nH]c3ccc(F)cc23)CC1)c1cc(C(F)(F)F)ccc1Cl nan
53341470 135387 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 451 4 1 3 4.6 O=C(N[C@H]1CC[C@H](CN2C(=O)Cc3cccnc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3727930 135387 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 451 4 1 3 4.6 O=C(N[C@H]1CC[C@H](CN2C(=O)Cc3cccnc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
53341172 136184 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 451 4 2 3 5.0 O=C(N[C@H]1CC[C@H](Cn2c(=O)[nH]c3ccccc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3732765 136184 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assayAntagonist activity against rat/human CRFR1 expressed in CHO cells assessed as inhibition of rat/human CRF-induced cAMP accumulation pre-incubated for 15 mins before CRF stimulation for 30 mins by FRET based HTRF assay
ChEMBL 451 4 2 3 5.0 O=C(N[C@H]1CC[C@H](Cn2c(=O)[nH]c3ccccc32)CC1)c1cc(C(F)(F)F)ccc1Cl nan
71456850 81516 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 424 9 0 6 5.2 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160166 81516 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 424 9 0 6 5.2 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
9822241 64009 8 None - 1 Human 7.0 pIC50 = 7.0 Functional
Inhibition of human CRF-1 receptor expressed in human IMR-32 cells assessed as effect on cAMP production by ELISA in presence of 3 nM CRFInhibition of human CRF-1 receptor expressed in human IMR-32 cells assessed as effect on cAMP production by ELISA in presence of 3 nM CRF
ChEMBL 399 8 1 6 5.0 CCC(CC)Nc1nc(C)c(-c2ccc(OC(F)(F)F)cc2OC)nc1OC 10.1021/jm200365y
CHEMBL1807053 64009 8 None - 1 Human 7.0 pIC50 = 7.0 Functional
Inhibition of human CRF-1 receptor expressed in human IMR-32 cells assessed as effect on cAMP production by ELISA in presence of 3 nM CRFInhibition of human CRF-1 receptor expressed in human IMR-32 cells assessed as effect on cAMP production by ELISA in presence of 3 nM CRF
ChEMBL 399 8 1 6 5.0 CCC(CC)Nc1nc(C)c(-c2ccc(OC(F)(F)F)cc2OC)nc1OC 10.1021/jm200365y
70692845 76607 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 422 10 0 5 6.0 CCCN(CCC)c1cccc2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063368 76607 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-stimulated intracellular cAMP accumulation after 30 mins by enzyme immunoassay
ChEMBL 422 10 0 5 6.0 CCCN(CCC)c1cccc2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
70692701 76296 0 None - 1 Rat 7.0 pIC50 = 7.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 392 5 0 6 4.1 CC[C@H](COC)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ncnc21 10.1016/j.bmcl.2012.06.034
CHEMBL2058605 76296 0 None - 1 Rat 7.0 pIC50 = 7.0 Functional
Antagonist activity at rat CFR1RAntagonist activity at rat CFR1R
ChEMBL 392 5 0 6 4.1 CC[C@H](COC)n1c(=O)c(C)nc2c(-c3ccc(Cl)cc3Cl)ncnc21 10.1016/j.bmcl.2012.06.034
59186874 126523 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 389 7 3 4 4.1 CCCc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n[nH]1 nan
CHEMBL3652101 126523 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.In Vitro Inhibition Assay: Chinese hamster ovary (CHO) cells expressing either the human recombinant CRF-1 or CRF-2a receptors (Chen et al., Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al., Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin (G418). For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) cAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions. CHO cells, previously cryopreserved, were thawed, centrifuged for 7 mins at 1200 rpm and resuspended in serum free media, then pipetted out onto clear bottomed black tissue culture treated 384-well microtitre plates (Corning Inc, US) at 2,000 cells per well. Compounds of the invention, prepared in DMSO, and subsequently diluted 50 fold in assay buffer (1x Hanks balanced salt solution, 0.2% (w/v) bovine serum albumin.
ChEMBL 389 7 3 4 4.1 CCCc1cc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n[nH]1 nan
71462234 81522 0 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 452 11 0 6 6.0 CCCN(CCC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160171 81522 0 None - 1 Human 7.0 pIC50 = 7 Functional
Antagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassayAntagonist activity at human CRF1 receptor expressed in HEK293 cells assessed as inhibition of CRF-induced intracellular cAMP production preincubated for 30 mins before CRF addition measured after 30 mins by enzyme immunoassay
ChEMBL 452 11 0 6 6.0 CCCN(CCC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
11223423 189542 30 None - 1 Human 7.1 pKd = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as effect on sauvagine-induced cAMP productionAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as effect on sauvagine-induced cAMP production
ChEMBL 404 4 1 6 3.1 COc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL514270 189542 30 None - 1 Human 7.1 pKd = 7.1 Functional
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as effect on sauvagine-induced cAMP productionAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as effect on sauvagine-induced cAMP production
ChEMBL 404 4 1 6 3.1 COc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
11546255 188117 0 None - 0 Human 9.7 pKi = 9.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 419 5 0 7 4.9 CCC(CC)c1cc(C)nn2c(-c3sc(N4CCOCC4)nc3Cl)c(C)nc12 10.1021/jm200365y
CHEMBL498311 188117 0 None - 0 Human 9.7 pKi = 9.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 419 5 0 7 4.9 CCC(CC)c1cc(C)nn2c(-c3sc(N4CCOCC4)nc3Cl)c(C)nc12 10.1021/jm200365y
54591779 66030 0 None - 0 Human 9.5 pKi = 9.5 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 429 8 1 7 4.6 COc1cc(OC(F)F)ccc1-n1c(C)nc2c(NC(C3CC3)C3CC3)nc(C)nc21 10.1016/j.bmcl.2011.08.040
CHEMBL1836947 66030 0 None - 0 Human 9.5 pKi = 9.5 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 429 8 1 7 4.6 COc1cc(OC(F)F)ccc1-n1c(C)nc2c(NC(C3CC3)C3CC3)nc(C)nc21 10.1016/j.bmcl.2011.08.040
44545165 66028 0 None - 0 Human 9.4 pKi = 9.4 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 433 7 1 6 5.3 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3Cl)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836945 66028 0 None - 0 Human 9.4 pKi = 9.4 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 433 7 1 6 5.3 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3Cl)c2n1 10.1016/j.bmcl.2011.08.040
9821586 168103 0 None - 1 Human 9.1 pKi = 9.1 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1021/jm200365y
CHEMBL432800 168103 0 None - 1 Human 9.1 pKi = 9.1 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1021/jm200365y
9884878 173025 18 None - 1 Human 8.8 pKi = 8.8 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2011.08.040
CHEMBL45187 173025 18 None - 1 Human 8.8 pKi = 8.8 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2011.08.040
11509708 18992 3 None - 1 Human 8.0 pKi = 8 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 CC[C@@H](Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
CHEMBL1287905 18992 3 None - 1 Human 8.0 pKi = 8 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 CC[C@@H](Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
11509709 19002 0 None - 0 Human 7.0 pKi = 7 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 CCC(Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12)c1nnc(C)o1 10.1016/j.bmcl.2010.10.095
CHEMBL1287996 19002 0 None - 0 Human 7.0 pKi = 7 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 CCC(Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12)c1nnc(C)o1 10.1016/j.bmcl.2010.10.095
45485065 197030 0 None - 0 Human 7.0 pKi = 7 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 378 7 0 7 3.5 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(C#N)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL567164 197030 0 None - 0 Human 7.0 pKi = 7 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 378 7 0 7 3.5 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(C#N)cc1C 10.1016/j.bmcl.2009.09.016
56663539 63939 0 None - 0 Human 7.0 pKi = 7.0 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1c(C)ncc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1021/jm200365y
CHEMBL1806727 63939 0 None - 0 Human 7.0 pKi = 7.0 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1c(C)ncc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1021/jm200365y
9980466 154128 0 None - 0 Human 8.0 pKi = 8.0 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 436 9 1 6 5.2 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1021/jm200365y
CHEMBL398531 154128 0 None - 0 Human 8.0 pKi = 8.0 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 436 9 1 6 5.2 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1021/jm200365y
10255153 77559 8 None - 1 Human 8.0 pKi = 8.0 Functional
Antagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulationAntagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulation
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087549 77559 8 None - 1 Human 8.0 pKi = 8.0 Functional
Antagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulationAntagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulation
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087567 77559 8 None - 1 Human 8.0 pKi = 8.0 Functional
Antagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulationAntagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulation
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
56835113 69617 0 None - 0 Human 8.0 pKi = 8.0 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 408 8 0 5 5.7 CCCCN(CC)c1nc(C)nc2c1c(C)c(COC)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2011.10.066
CHEMBL1934751 69617 0 None - 0 Human 8.0 pKi = 8.0 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 408 8 0 5 5.7 CCCCN(CC)c1nc(C)nc2c1c(C)c(COC)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2011.10.066
56672697 66023 0 None - 0 Human 8.0 pKi = 8.0 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 367 5 1 5 4.7 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(Cl)cc3)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836940 66023 0 None - 0 Human 8.0 pKi = 8.0 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 367 5 1 5 4.7 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(Cl)cc3)c2n1 10.1016/j.bmcl.2011.08.040
45485057 197008 0 None - 0 Human 6.0 pKi = 6.0 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 355 6 2 7 2.9 CC[C@H](CO)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL566939 197008 0 None - 0 Human 6.0 pKi = 6.0 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 355 6 2 7 2.9 CC[C@H](CO)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
45485022 197065 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 0 7 3.2 CCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL567383 197065 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 0 7 3.2 CCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
44446725 168953 0 None - 1 Human 7.9 pKi = 7.9 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL438888 168953 0 None - 1 Human 7.9 pKi = 7.9 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
3496 1180 42 None - 1 Rat 7.9 pKi = 7.9 Functional
Antagonist activity at CRF1 receptor in rat cortical membrane assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillationAntagonist activity at CRF1 receptor in rat cortical membrane assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
9862166 1180 42 None - 1 Rat 7.9 pKi = 7.9 Functional
Antagonist activity at CRF1 receptor in rat cortical membrane assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillationAntagonist activity at CRF1 receptor in rat cortical membrane assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
CHEMBL270948 1180 42 None - 1 Rat 7.9 pKi = 7.9 Functional
Antagonist activity at CRF1 receptor in rat cortical membrane assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillationAntagonist activity at CRF1 receptor in rat cortical membrane assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
3496 1180 42 None - 1 Human 7.9 pKi = 7.9 Functional
Antagonist activity at human CRF1 receptor assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation countingAntagonist activity at human CRF1 receptor assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation counting
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
9862166 1180 42 None - 1 Human 7.9 pKi = 7.9 Functional
Antagonist activity at human CRF1 receptor assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation countingAntagonist activity at human CRF1 receptor assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation counting
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
CHEMBL270948 1180 42 None - 1 Human 7.9 pKi = 7.9 Functional
Antagonist activity at human CRF1 receptor assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation countingAntagonist activity at human CRF1 receptor assessed as oCRF-stimulated adenylate cyclase activity after 15 mins by liquid scintillation counting
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
3520 3267 54 None - 1 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2011.08.040
9821250 3267 54 None - 1 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2011.08.040
CHEMBL309138 3267 54 None - 1 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2011.08.040
44545284 66029 0 None - 0 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 397 6 1 6 4.7 COc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)c(Cl)c1 10.1016/j.bmcl.2011.08.040
CHEMBL1836946 66029 0 None - 0 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 397 6 1 6 4.7 COc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)c(Cl)c1 10.1016/j.bmcl.2011.08.040
45485056 197007 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 422 8 2 10 3.4 CCCNCc1nc(Nc2nc(C)nc3c2c(C)nn3-c2ccc(OC)cc2C)no1 10.1016/j.bmcl.2009.09.016
CHEMBL566938 197007 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 422 8 2 10 3.4 CCCNCc1nc(Nc2nc(C)nc3c2c(C)nn3-c2ccc(OC)cc2C)no1 10.1016/j.bmcl.2009.09.016
45485032 197002 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 1 7 3.0 CCCN(CCO)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL566910 197002 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 1 7 3.0 CCCN(CCO)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
45485040 197284 0 None - 0 Human 7.9 pKi = 7.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 383 8 0 7 3.6 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL568606 197284 0 None - 0 Human 7.9 pKi = 7.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 383 8 0 7 3.6 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
45485040 197284 0 None - 0 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 383 8 0 7 3.6 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2011.08.040
CHEMBL568606 197284 0 None - 0 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 383 8 0 7 3.6 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2011.08.040
45484977 197290 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 383 9 1 7 4.1 CCCC(CCOC)Nc1nc(C)nc2c1cnn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL568656 197290 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 383 9 1 7 4.1 CCCC(CCOC)Nc1nc(C)nc2c1cnn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
45485009 198436 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 1 7 3.6 CC[C@@H](COC)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL577239 198436 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 1 7 3.6 CC[C@@H](COC)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
44543774 66016 0 None - 0 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 377 6 1 6 4.4 COc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)c(C)c1 10.1016/j.bmcl.2011.08.040
CHEMBL1836933 66016 0 None - 0 Human 7.9 pKi = 7.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 377 6 1 6 4.4 COc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)c(C)c1 10.1016/j.bmcl.2011.08.040
56658150 65617 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 411 6 1 7 3.4 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(S(C)(=O)=O)cc3)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1834003 65617 0 None - 0 Human 6.9 pKi = 6.9 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 411 6 1 7 3.4 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(S(C)(=O)=O)cc3)c2n1 10.1016/j.bmcl.2011.08.040
45485033 197003 0 None - 0 Human 5.9 pKi = 5.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 410 7 0 7 3.1 CCCN(CC(=O)N(C)C)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL566911 197003 0 None - 0 Human 5.9 pKi = 5.9 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 410 7 0 7 3.1 CCCN(CC(=O)N(C)C)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
56682683 66017 0 None - 0 Human 6.8 pKi = 6.8 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 393 8 1 7 3.9 COCc1nc2c(NC(C3CC3)C3CC3)nc(C)nc2n1-c1ccc(OC)cc1 10.1016/j.bmcl.2011.08.040
CHEMBL1836934 66017 0 None - 0 Human 6.8 pKi = 6.8 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 393 8 1 7 3.9 COCc1nc2c(NC(C3CC3)C3CC3)nc(C)nc2n1-c1ccc(OC)cc1 10.1016/j.bmcl.2011.08.040
18691322 4661 0 None - 0 Human 6.8 pKi = 6.8 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 397 2 0 5 5.1 Cc1cc(C)c(-n2nnc3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(C)c1 10.1016/s0960-894x(99)00133-x
CHEMBL10315 4661 0 None - 0 Human 6.8 pKi = 6.8 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 397 2 0 5 5.1 Cc1cc(C)c(-n2nnc3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(C)c1 10.1016/s0960-894x(99)00133-x
45484988 197301 0 None - 0 Human 7.8 pKi = 7.8 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 400 9 0 9 2.7 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)nc1OC 10.1016/j.bmcl.2009.09.016
CHEMBL568685 197301 0 None - 0 Human 7.8 pKi = 7.8 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 400 9 0 9 2.7 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)nc1OC 10.1016/j.bmcl.2009.09.016
45484992 198902 0 None - 0 Human 6.7 pKi = 6.7 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 397 8 0 8 3.1 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1cnc(N(C)C)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL584472 198902 0 None - 0 Human 6.7 pKi = 6.7 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 397 8 0 8 3.1 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1cnc(N(C)C)cc1C 10.1016/j.bmcl.2009.09.016
54591854 66015 0 None - 0 Human 7.7 pKi = 7.7 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 363 6 1 6 4.0 COc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
CHEMBL1836932 66015 0 None - 0 Human 7.7 pKi = 7.7 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 363 6 1 6 4.0 COc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
45485023 198752 0 None - 0 Human 6.7 pKi = 6.7 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL583005 198752 0 None - 0 Human 6.7 pKi = 6.7 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
3533 1206 24 None - 0 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1021/jm200365y
5282340 1206 24 None - 0 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1021/jm200365y
CHEMBL291657 1206 24 None - 0 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1021/jm200365y
3499 1448 28 None -25 2 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm200365y
9909468 1448 28 None -25 2 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm200365y
CHEMBL44698 1448 28 None -25 2 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm200365y
176157 2738 28 None - 2 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm200365y
3512 2738 28 None - 2 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm200365y
CHEMBL45281 2738 28 None - 2 Human 8.7 pKi = 8.7 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm200365y
44266581 4427 0 None - 0 Human 8.7 pKi = 8.7 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 398 6 1 4 6.0 CCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1016/s0960-894x(99)00133-x
CHEMBL10154 4427 0 None - 0 Human 8.7 pKi = 8.7 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 398 6 1 4 6.0 CCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1016/s0960-894x(99)00133-x
3495 1175 28 None -14 2 Human 8.6 pKi = 8.6 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(99)00133-x
5311055 1175 28 None -14 2 Human 8.6 pKi = 8.6 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(99)00133-x
CHEMBL9946 1175 28 None -14 2 Human 8.6 pKi = 8.6 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(99)00133-x
56662343 66025 0 None - 0 Human 7.7 pKi = 7.7 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 377 7 1 6 4.4 CCOc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
CHEMBL1836942 66025 0 None - 0 Human 7.7 pKi = 7.7 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 377 7 1 6 4.4 CCOc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
18691310 4607 0 None - 0 Human 6.7 pKi = 6.7 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 508 4 1 7 5.3 COc1cc(Br)c(-n2c(O)nc3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(OC)c1 10.1016/s0960-894x(99)00133-x
CHEMBL10279 4607 0 None - 0 Human 6.7 pKi = 6.7 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 508 4 1 7 5.3 COc1cc(Br)c(-n2c(O)nc3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(OC)c1 10.1016/s0960-894x(99)00133-x
44266488 98524 0 None - 0 Human 7.7 pKi = 7.7 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 493 4 0 7 5.0 COc1cc(Br)c(-n2nnc3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(OC)c1 10.1016/s0960-894x(99)00133-x
CHEMBL276263 98524 0 None - 0 Human 7.7 pKi = 7.7 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 493 4 0 7 5.0 COc1cc(Br)c(-n2nnc3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(OC)c1 10.1016/s0960-894x(99)00133-x
45485034 197004 0 None - 0 Human 6.7 pKi = 6.7 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 1 7 3.6 CC[C@H](COC)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL566912 197004 0 None - 0 Human 6.7 pKi = 6.7 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 1 7 3.6 CC[C@H](COC)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
44446726 94834 0 None - 0 Human 7.7 pKi = 7.7 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 476 11 0 3 7.5 CCCN(CCC)c1c(C)nc(-c2c(CC(F)F)cc(CC(F)F)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253699 94834 0 None - 0 Human 7.7 pKi = 7.7 Functional
Antagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulationAntagonist activity at CRF1 receptor expressed in mouse AtT20 cells assessed as inhibition of sauvagine-stimulated cAMP accumulation
ChEMBL 476 11 0 3 7.5 CCCN(CCC)c1c(C)nc(-c2c(CC(F)F)cc(CC(F)F)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
18691303 4301 0 None - 0 Human 7.6 pKi = 7.6 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 512 6 1 7 5.9 COc1cc(Br)c(Nc2nc(C)nc(-c3ccccc3C(F)(F)F)c2[N+](=O)[O-])c(OC)c1 10.1016/s0960-894x(99)00133-x
CHEMBL10080 4301 0 None - 0 Human 7.6 pKi = 7.6 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 512 6 1 7 5.9 COc1cc(Br)c(Nc2nc(C)nc(-c3ccccc3C(F)(F)F)c2[N+](=O)[O-])c(OC)c1 10.1016/s0960-894x(99)00133-x
52947302 18988 0 None - 0 Human 7.6 pKi = 7.6 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 392 5 1 8 4.2 COc1ccc(-c2c(C)nn3c(NC(C)c4nc(C)no4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
CHEMBL1287878 18988 0 None - 0 Human 7.6 pKi = 7.6 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 392 5 1 8 4.2 COc1ccc(-c2c(C)nn3c(NC(C)c4nc(C)no4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
45484976 197064 0 None - 0 Human 5.6 pKi = 5.6 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 420 8 2 9 3.3 CCCNCc1cncn1Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL567382 197064 0 None - 0 Human 5.6 pKi = 5.6 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 420 8 2 9 3.3 CCCNCc1cncn1Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
11697131 19003 0 None - 0 Human 6.6 pKi = 6.6 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.1 COc1ccc(-c2c(C)nn3c(NC(C)Cc4nnc(C)o4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
CHEMBL1287997 19003 0 None - 0 Human 6.6 pKi = 6.6 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.1 COc1ccc(-c2c(C)nn3c(NC(C)Cc4nnc(C)o4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
56682684 66021 0 None - 0 Human 6.6 pKi = 6.6 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 439 7 1 6 5.2 COc1ccc(-n2c(C3CC(F)(F)C3)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
CHEMBL1836938 66021 0 None - 0 Human 6.6 pKi = 6.6 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 439 7 1 6 5.2 COc1ccc(-n2c(C3CC(F)(F)C3)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
45485079 197091 0 None - 0 Human 6.6 pKi = 6.6 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 396 8 1 7 2.7 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(C(N)=O)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL567538 197091 0 None - 0 Human 6.6 pKi = 6.6 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 396 8 1 7 2.7 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(C(N)=O)cc1C 10.1016/j.bmcl.2009.09.016
3495 1175 28 None -14 2 Human 8.5 pKi = 8.5 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm200365y
5311055 1175 28 None -14 2 Human 8.5 pKi = 8.5 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm200365y
CHEMBL9946 1175 28 None -14 2 Human 8.5 pKi = 8.5 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm200365y
3520 3267 54 None - 1 Human 8.5 pKi = 8.5 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm200365y
9821250 3267 54 None - 1 Human 8.5 pKi = 8.5 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm200365y
CHEMBL309138 3267 54 None - 1 Human 8.5 pKi = 8.5 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm200365y
9955329 207830 0 None - 0 Human 8.5 pKi = 8.5 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 448 8 0 8 3.9 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00133-x
CHEMBL9633 207830 0 None - 0 Human 8.5 pKi = 8.5 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 448 8 0 8 3.9 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00133-x
9934089 5007 0 None - 0 Human 8.4 pKi = 8.4 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 462 9 0 8 3.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00133-x
CHEMBL10504 5007 0 None - 0 Human 8.4 pKi = 8.4 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 462 9 0 8 3.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00133-x
3520 3267 54 None - 1 Human 8.4 pKi = 8.4 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2010.10.095
9821250 3267 54 None - 1 Human 8.4 pKi = 8.4 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2010.10.095
CHEMBL309138 3267 54 None - 1 Human 8.4 pKi = 8.4 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2010.10.095
56658860 66018 0 None - 0 Human 6.5 pKi = 6.5 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 403 8 1 6 4.7 COc1ccc(-n2c(CC3CC3)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
CHEMBL1836935 66018 0 None - 0 Human 6.5 pKi = 6.5 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 403 8 1 6 4.7 COc1ccc(-n2c(CC3CC3)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
11509641 18993 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 404 5 1 8 4.1 COc1ccc(-c2c(C)nn3c(NC4(c5nc(C)no5)CC4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
CHEMBL1287936 18993 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 404 5 1 8 4.1 COc1ccc(-c2c(C)nn3c(NC4(c5nc(C)no5)CC4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
11531570 18999 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.1 COc1ccc(-c2c(C)nn3c(NC(C)Cc4nc(C)no4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
CHEMBL1287966 18999 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.1 COc1ccc(-c2c(C)nn3c(NC(C)Cc4nc(C)no4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
45485105 197428 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 367 8 1 6 4.8 CCCC(CCC)Nc1nc(C)nc2c1cnn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL569666 197428 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 367 8 1 6 4.8 CCCC(CCC)Nc1nc(C)nc2c1cnn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
177990 426 23 None - 1 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.bmcl.2011.10.066
3489 426 23 None - 1 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.bmcl.2011.10.066
CHEMBL296641 426 23 None - 1 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.bmcl.2011.10.066
46175148 66032 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 363 6 1 6 4.0 COc1ccc(-n2ncc3c(NC(C4CC4)C4CC4)nc(C)nc32)c(C)c1 10.1016/j.bmcl.2011.08.040
CHEMBL1836950 66032 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 363 6 1 6 4.0 COc1ccc(-n2ncc3c(NC(C4CC4)C4CC4)nc(C)nc32)c(C)c1 10.1016/j.bmcl.2011.08.040
18691329 4403 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 506 4 0 6 5.9 COc1cc(Br)c(-n2c(C)nc3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(OC)c1 10.1016/s0960-894x(99)00133-x
CHEMBL10142 4403 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 506 4 0 6 5.9 COc1cc(Br)c(-n2c(C)nc3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(OC)c1 10.1016/s0960-894x(99)00133-x
44266555 4460 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 502 3 0 5 7.5 CSc1nn(-c2c(Cl)cc(Cl)cc2Cl)c2nc(C)nc(-c3ccccc3C(F)(F)F)c12 10.1016/s0960-894x(99)00133-x
CHEMBL10174 4460 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 502 3 0 5 7.5 CSc1nn(-c2c(Cl)cc(Cl)cc2Cl)c2nc(C)nc(-c3ccccc3C(F)(F)F)c12 10.1016/s0960-894x(99)00133-x
45485086 196924 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 381 8 1 6 5.1 CCCC(CCC)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL566279 196924 0 None - 0 Human 7.5 pKi = 7.5 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 381 8 1 6 5.1 CCCC(CCC)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
10375 2739 18 None - 0 Human 8.4 pKi = 8.4 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm200365y
9888194 2739 18 None - 0 Human 8.4 pKi = 8.4 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm200365y
CHEMBL188907 2739 18 None - 0 Human 8.4 pKi = 8.4 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm200365y
45485080 197124 0 None - 0 Human 6.4 pKi = 6.4 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 420 8 2 9 3.3 CCCNCc1nccn1Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL567741 197124 0 None - 0 Human 6.4 pKi = 6.4 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 420 8 2 9 3.3 CCCNCc1nccn1Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
45485073 196777 0 None - 0 Human 7.4 pKi = 7.4 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 353 6 1 6 4.4 CCC(CC)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL565442 196777 0 None - 0 Human 7.4 pKi = 7.4 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 353 6 1 6 4.4 CCC(CC)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
45484980 197293 0 None - 0 Human 7.4 pKi = 7.4 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 384 8 0 8 3.0 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)nc1C 10.1016/j.bmcl.2009.09.016
CHEMBL568665 197293 0 None - 0 Human 7.4 pKi = 7.4 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 384 8 0 8 3.0 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)nc1C 10.1016/j.bmcl.2009.09.016
56676057 66014 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 363 6 1 6 4.0 COc1ccc(-n2cnc3c(NC(C4CC4)C4CC4)nc(C)nc32)c(C)c1 10.1016/j.bmcl.2011.08.040
CHEMBL1836931 66014 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 363 6 1 6 4.0 COc1ccc(-n2cnc3c(NC(C4CC4)C4CC4)nc(C)nc32)c(C)c1 10.1016/j.bmcl.2011.08.040
44545161 66027 0 None - 0 Human 8.3 pKi = 8.3 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 399 7 1 6 4.6 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836944 66027 0 None - 0 Human 8.3 pKi = 8.3 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 399 7 1 6 4.6 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3)c2n1 10.1016/j.bmcl.2011.08.040
11589539 18987 0 None - 0 Human 8.3 pKi = 8.3 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 0 8 4.0 CCN(Cc1nc(C)no1)c1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2010.10.095
CHEMBL1287877 18987 0 None - 0 Human 8.3 pKi = 8.3 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 0 8 4.0 CCN(Cc1nc(C)no1)c1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2010.10.095
10367821 4305 0 None - 0 Human 8.3 pKi = 8.3 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 478 5 0 4 6.9 CCN(c1nc(C)nc(-c2ccccc2C(F)(F)F)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00133-x
CHEMBL10082 4305 0 None - 0 Human 8.3 pKi = 8.3 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 478 5 0 4 6.9 CCN(c1nc(C)nc(-c2ccccc2C(F)(F)F)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00133-x
52944875 18998 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 418 5 1 8 4.5 COc1ccc(-c2c(C)nn3c(NC4(c5nc(C)no5)CCC4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
CHEMBL1287965 18998 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 418 5 1 8 4.5 COc1ccc(-c2c(C)nn3c(NC4(c5nc(C)no5)CCC4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
52947334 19007 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 420 6 1 9 4.0 CCC(Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
CHEMBL1288027 19007 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 420 6 1 9 4.0 CCC(Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
11531898 19012 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 422 7 1 9 4.3 CCC(Nc1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
CHEMBL1288058 19012 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 422 7 1 9 4.3 CCC(Nc1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
57390674 69616 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 392 7 0 5 5.4 CCCCN(CC)c1nc(C)nc2c1c(C)c(C=O)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2011.10.066
CHEMBL1934750 69616 0 None - 0 Human 7.3 pKi = 7.3 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 392 7 0 5 5.4 CCCCN(CC)c1nc(C)nc2c1c(C)c(C=O)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2011.10.066
45485042 197367 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 2 7 3.3 CCC[C@@H](CO)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL569202 197367 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 2 7 3.3 CCC[C@@H](CO)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
45485008 198370 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 397 8 1 8 2.1 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(C(N)=O)nc1C 10.1016/j.bmcl.2009.09.016
CHEMBL576639 198370 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 397 8 1 8 2.1 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(C(N)=O)nc1C 10.1016/j.bmcl.2009.09.016
56835112 69615 0 None - 0 Human 8.2 pKi = 8.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 394 7 1 5 5.1 CCCCN(CC)c1nc(C)nc2c1c(C)c(CO)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2011.10.066
CHEMBL1934749 69615 0 None - 0 Human 8.2 pKi = 8.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assayAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells by cAMP assay
ChEMBL 394 7 1 5 5.1 CCCCN(CC)c1nc(C)nc2c1c(C)c(CO)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2011.10.066
10378 3985 37 None - 1 Human 8.2 pKi = 8.2 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 10.1016/j.bmcl.2010.10.095
11596613 3985 37 None - 1 Human 8.2 pKi = 8.2 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 10.1016/j.bmcl.2010.10.095
CHEMBL1287935 3985 37 None - 1 Human 8.2 pKi = 8.2 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 10.1016/j.bmcl.2010.10.095
DB12512 3985 37 None - 1 Human 8.2 pKi = 8.2 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 10.1016/j.bmcl.2010.10.095
18691308 4326 0 None - 0 Human 7.2 pKi = 7.2 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 482 5 2 6 5.6 COc1cc(Br)c(Nc2nc(C)nc(-c3ccccc3C(F)(F)F)c2N)c(OC)c1 10.1016/s0960-894x(99)00133-x
CHEMBL10091 4326 0 None - 0 Human 7.2 pKi = 7.2 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 482 5 2 6 5.6 COc1cc(Br)c(Nc2nc(C)nc(-c3ccccc3C(F)(F)F)c2N)c(OC)c1 10.1016/s0960-894x(99)00133-x
56672696 66019 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 405 8 1 6 4.9 COc1ccc(-n2c(CC(C)C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
CHEMBL1836936 66019 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 405 8 1 6 4.9 COc1ccc(-n2c(CC(C)C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
56682685 66022 0 None - 0 Human 7.2 pKi = 7.2 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 358 5 1 6 3.9 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(C#N)cc3)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836939 66022 0 None - 0 Human 7.2 pKi = 7.2 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 358 5 1 6 3.9 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(C#N)cc3)c2n1 10.1016/j.bmcl.2011.08.040
45485045 197249 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 355 6 2 7 2.9 CC[C@@H](CO)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL568397 197249 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 355 6 2 7 2.9 CC[C@@H](CO)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
11538121 18984 0 None - 0 Human 7.2 pKi = 7.2 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 378 5 1 8 3.6 COc1ccc(-c2c(C)nn3c(NCc4nc(C)no4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
CHEMBL1287848 18984 0 None - 0 Human 7.2 pKi = 7.2 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 378 5 1 8 3.6 COc1ccc(-c2c(C)nn3c(NCc4nc(C)no4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
45485078 198782 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 389 7 0 8 3.0 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(C#N)cc1C#N 10.1016/j.bmcl.2009.09.016
CHEMBL583223 198782 0 None - 0 Human 6.2 pKi = 6.2 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 389 7 0 8 3.0 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(C#N)cc1C#N 10.1016/j.bmcl.2009.09.016
44545396 66031 0 None - 0 Human 8.2 pKi = 8.2 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 417 7 1 6 4.8 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3F)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836948 66031 0 None - 0 Human 8.2 pKi = 8.2 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 417 7 1 6 4.8 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3F)c2n1 10.1016/j.bmcl.2011.08.040
10377 1179 27 None 3 2 Rat 8.1 pKi = 8.1 Functional
Antagonist activity at rat cortex CRF1 receptor assessed as inhibition of CRF-stimulated adenylate cyclase activityAntagonist activity at rat cortex CRF1 receptor assessed as inhibition of CRF-stimulated adenylate cyclase activity
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
9818802 1179 27 None 3 2 Rat 8.1 pKi = 8.1 Functional
Antagonist activity at rat cortex CRF1 receptor assessed as inhibition of CRF-stimulated adenylate cyclase activityAntagonist activity at rat cortex CRF1 receptor assessed as inhibition of CRF-stimulated adenylate cyclase activity
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
CHEMBL270738 1179 27 None 3 2 Rat 8.1 pKi = 8.1 Functional
Antagonist activity at rat cortex CRF1 receptor assessed as inhibition of CRF-stimulated adenylate cyclase activityAntagonist activity at rat cortex CRF1 receptor assessed as inhibition of CRF-stimulated adenylate cyclase activity
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
11545949 18991 10 None - 0 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 CCC(Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
CHEMBL1287904 18991 10 None - 0 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.6 CCC(Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12)c1nc(C)no1 10.1016/j.bmcl.2010.10.095
45485064 198785 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 399 9 0 8 3.3 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1OC 10.1016/j.bmcl.2009.09.016
CHEMBL583237 198785 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 399 9 0 8 3.3 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1OC 10.1016/j.bmcl.2009.09.016
45485035 196886 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 2 7 3.3 CCC[C@H](CO)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL566073 196886 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 369 7 2 7 3.3 CCC[C@H](CO)Nc1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
52947738 19006 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.1 COc1ccc(-c2c(C)nn3c(NC(C)Cc4noc(C)n4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
CHEMBL1288026 19006 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptorAntagonist activity at human recombinant CRF1 receptor
ChEMBL 406 6 1 8 4.1 COc1ccc(-c2c(C)nn3c(NC(C)Cc4noc(C)n4)cc(C)nc23)c(C)c1 10.1016/j.bmcl.2010.10.095
3520 3267 54 None - 1 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulationAntagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulation
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm300259r
9821250 3267 54 None - 1 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulationAntagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulation
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm300259r
CHEMBL309138 3267 54 None - 1 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulationAntagonist activity at human CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF-stimulated cAMP accumulation
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm300259r
10377 1179 27 None -3 2 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human CRF1 receptor endogenously expressed in human IMR32 cellsAntagonist activity at human CRF1 receptor endogenously expressed in human IMR32 cells
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
9818802 1179 27 None -3 2 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human CRF1 receptor endogenously expressed in human IMR32 cellsAntagonist activity at human CRF1 receptor endogenously expressed in human IMR32 cells
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
CHEMBL270738 1179 27 None -3 2 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human CRF1 receptor endogenously expressed in human IMR32 cellsAntagonist activity at human CRF1 receptor endogenously expressed in human IMR32 cells
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
45485050 197206 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 422 8 2 10 3.4 CCCNCc1noc(Nc2nc(C)nc3c2c(C)nn3-c2ccc(OC)cc2C)n1 10.1016/j.bmcl.2009.09.016
CHEMBL568188 197206 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 422 8 2 10 3.4 CCCNCc1noc(Nc2nc(C)nc3c2c(C)nn3-c2ccc(OC)cc2C)n1 10.1016/j.bmcl.2009.09.016
45484981 198373 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 339 6 1 6 4.0 CCC(CC)Nc1nc(C)nc2c1cnn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL576664 198373 0 None - 0 Human 7.1 pKi = 7.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 339 6 1 6 4.0 CCC(CC)Nc1nc(C)nc2c1cnn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2009.09.016
56662342 66020 0 None - 0 Human 6.1 pKi = 6.1 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 419 7 1 7 4.6 COc1ccc(-n2c(C3CCCO3)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
CHEMBL1836937 66020 0 None - 0 Human 6.1 pKi = 6.1 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 419 7 1 7 4.6 COc1ccc(-n2c(C3CCCO3)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
24971237 188049 0 None - 1 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 380 8 0 6 4.7 CCC(CC)Oc1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1021/jm200365y
CHEMBL497653 188049 0 None - 1 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human CRF-1 receptorAntagonist activity at human CRF-1 receptor
ChEMBL 380 8 0 6 4.7 CCC(CC)Oc1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1021/jm200365y
22004628 198306 0 None - 0 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 365 6 0 5 5.0 CCCCN(CC)c1nc(C)nc2c1c(C)nn2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2009.09.016
CHEMBL576049 198306 0 None - 0 Human 8.1 pKi = 8.1 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 365 6 0 5 5.0 CCCCN(CC)c1nc(C)nc2c1c(C)nn2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2009.09.016
56672698 66026 0 None - 0 Human 8.1 pKi = 8.1 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 417 6 1 6 4.9 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)(F)F)cc3)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836943 66026 0 None - 0 Human 8.1 pKi = 8.1 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 417 6 1 6 4.9 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)(F)F)cc3)c2n1 10.1016/j.bmcl.2011.08.040
18691298 98159 0 None - 0 Human 8.0 pKi = 8.0 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 423 2 0 3 7.0 Cc1cc(C)c(-n2c(C)c(C)c3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(C)c1 10.1016/s0960-894x(99)00133-x
CHEMBL273839 98159 0 None - 0 Human 8.0 pKi = 8.0 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 423 2 0 3 7.0 Cc1cc(C)c(-n2c(C)c(C)c3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(C)c1 10.1016/s0960-894x(99)00133-x
44545281 66024 0 None - 0 Human 7.0 pKi = 7.0 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 351 5 1 5 4.2 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(F)cc3)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836941 66024 0 None - 0 Human 7.0 pKi = 7.0 Functional
Antagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formationAntagonist activity at recombinant human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP formation
ChEMBL 351 5 1 5 4.2 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(F)cc3)c2n1 10.1016/j.bmcl.2011.08.040
18691301 4324 0 None - 0 Human 7.0 pKi = 7.0 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 522 4 0 7 4.9 COc1cc(Br)c(-n2c(=O)n(C)c3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(OC)c1 10.1016/s0960-894x(99)00133-x
CHEMBL10090 4324 0 None - 0 Human 7.0 pKi = 7.0 Functional
Antagonistic activity for Corticotropin releasing factor receptor 1Antagonistic activity for Corticotropin releasing factor receptor 1
ChEMBL 522 4 0 7 4.9 COc1cc(Br)c(-n2c(=O)n(C)c3c(-c4ccccc4C(F)(F)F)nc(C)nc32)c(OC)c1 10.1016/s0960-894x(99)00133-x
45485041 197285 0 None - 0 Human 6.0 pKi = 6 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 422 8 2 10 3.4 CCCNCc1nnc(Nc2nc(C)nc3c2c(C)nn3-c2ccc(OC)cc2C)o1 10.1016/j.bmcl.2009.09.016
CHEMBL568607 197285 0 None - 0 Human 6.0 pKi = 6 Functional
Antagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP productionAntagonist activity at human recombinant CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-induced cAMP production
ChEMBL 422 8 2 10 3.4 CCCNCc1nnc(Nc2nc(C)nc3c2c(C)nn3-c2ccc(OC)cc2C)o1 10.1016/j.bmcl.2009.09.016
10379 3059 39 None -1 3 Rat 6.9 pIC50 = 6.9 Functional
Antagonism of CRF-mediated ACTH production in rat pituitary cells.Antagonism of CRF-mediated ACTH production in rat pituitary cells.
Guide to Pharmacology 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 28174066
9884366 3059 39 None -1 3 Rat 6.9 pIC50 = 6.9 Functional
Antagonism of CRF-mediated ACTH production in rat pituitary cells.Antagonism of CRF-mediated ACTH production in rat pituitary cells.
Guide to Pharmacology 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 28174066
CHEMBL482950 3059 39 None -1 3 Rat 6.9 pIC50 = 6.9 Functional
Antagonism of CRF-mediated ACTH production in rat pituitary cells.Antagonism of CRF-mediated ACTH production in rat pituitary cells.
Guide to Pharmacology 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 28174066
DB12572 3059 39 None -1 3 Rat 6.9 pIC50 = 6.9 Functional
Antagonism of CRF-mediated ACTH production in rat pituitary cells.Antagonism of CRF-mediated ACTH production in rat pituitary cells.
Guide to Pharmacology 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 28174066
3498 1204 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 476 7 0 5 7.2 CCN(c1ccc(cc1SC)C(C)C)c1nc(cc(n1)C)N1CCC(=CC1)c1cccc(c1)F 10357258
9849313 1204 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 476 7 0 5 7.2 CCN(c1ccc(cc1SC)C(C)C)c1nc(cc(n1)C)N1CCC(=CC1)c1cccc(c1)F 10357258
CHEMBL297986 1204 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 476 7 0 5 7.2 CCN(c1ccc(cc1SC)C(C)C)c1nc(cc(n1)C)N1CCC(=CC1)c1cccc(c1)F 10357258
3496 1180 42 None - 1 Rat 8.3 pIC50 = 8.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18288792
9862166 1180 42 None - 1 Rat 8.3 pIC50 = 8.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18288792
CHEMBL270948 1180 42 None - 1 Rat 8.3 pIC50 = 8.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18288792
10376 2930 4 None 1 2 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 21865047
9801039 2930 4 None 1 2 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 21865047
CHEMBL1819077 2930 4 None 1 2 Human 8.4 pIC50 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 21865047
16133798 506 0 None -1 2 Human 9.1 pIC50 = 9.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12361401
925 506 0 None -1 2 Human 9.1 pIC50 = 9.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12361401
3495 1175 28 None 14 2 Rat 9.9 pIC50 = 9.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 8874139
5311055 1175 28 None 14 2 Rat 9.9 pIC50 = 9.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 8874139
CHEMBL9946 1175 28 None 14 2 Rat 9.9 pIC50 = 9.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 8874139
10335 507 0 None -389 2 Human 6.3 pIC50 > 6.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12361401
90488758 507 0 None -389 2 Human 6.3 pIC50 > 6.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 12361401




Ligands (move mouse cursor over ligand name to see structure) Receptor Assay information Chemical information
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CHEMBL264275 210611 0 None - 0 Mouse 7.0 pEC50 = 7 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)C(C)C)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL442112 213906 0 None - 0 Mouse 7.0 pEC50 = 7.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL263862 210596 0 None - 0 Mouse 7.0 pEC50 = 7.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL427923 213394 0 None - 0 Mouse 7.0 pEC50 = 7.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL427811 213386 0 None - 0 Mouse 7.0 pEC50 = 7.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL437089 213704 0 None - 0 Mouse 7.0 pEC50 = 7.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL438391 213768 0 None - 0 Mouse 6.9 pEC50 = 6.9 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL414130 213112 0 None - 0 Mouse 6.8 pEC50 = 6.8 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL439883 213849 0 None - 1 Mouse 7.8 pEC50 = 7.8 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL438220 213756 0 None - 0 Mouse 6.7 pEC50 = 6.7 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL410568 212826 0 None - 0 Mouse 6.7 pEC50 = 6.7 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
44362115 1169 0 None - 0 Mouse 7.7 pEC50 = 7.7 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None None 10.1021/jm049490m
6967 1169 0 None - 0 Mouse 7.7 pEC50 = 7.7 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None None 10.1021/jm049490m
CHEMBL1201609 1169 0 None - 0 Mouse 7.7 pEC50 = 7.7 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None None 10.1021/jm049490m
CHEMBL440057 1169 0 None - 0 Mouse 7.7 pEC50 = 7.7 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None None 10.1021/jm049490m
CHEMBL428127 213417 0 None - 0 Mouse 6.7 pEC50 = 6.7 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL415130 213170 0 None - 0 Mouse 6.6 pEC50 = 6.6 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL438601 213782 0 None - 0 Mouse 6.6 pEC50 = 6.6 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)C(C)C)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL412296 212982 0 None - 0 Mouse 6.5 pEC50 = 6.5 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL429403 213528 0 None - 0 Mouse 6.5 pEC50 = 6.5 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL427611 213355 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL428809 213474 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL268549 210758 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL428296 213435 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL409748 212781 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL427792 213383 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL438760 213794 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL413414 213064 0 None - 0 Mouse 7.3 pEC50 = 7.3 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL267635 210726 0 None - 0 Mouse 7.3 pEC50 = 7.3 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL429547 213539 0 None - 0 Mouse 6.3 pEC50 = 6.3 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL410814 212844 0 None - 0 Mouse 6.2 pEC50 = 6.2 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL429719 213543 0 None - 0 Mouse 6.2 pEC50 = 6.2 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL438210 213754 0 None - 0 Mouse 6.2 pEC50 = 6.2 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL411590 212950 0 None - 0 Mouse 7.2 pEC50 = 7.2 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL438948 213816 0 None - 0 Mouse 7.2 pEC50 = 7.2 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL438928 213812 0 None - 0 Mouse 7.2 pEC50 = 7.2 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL412026 212971 0 None - 0 Mouse 7.2 pEC50 = 7.2 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL437289 213715 0 None - 0 Mouse 6.2 pEC50 = 6.2 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL439102 213822 0 None - 0 Mouse 6.1 pEC50 = 6.1 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL438939 213815 0 None - 0 Mouse 7.1 pEC50 = 7.1 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL428824 213477 0 None - 0 Mouse 7.1 pEC50 = 7.1 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL436912 213696 0 None - 0 Mouse 7.1 pEC50 = 7.1 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL436914 213697 0 None - 0 Mouse 7.1 pEC50 = 7.1 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)C(C)C)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL430078 213608 0 None - 0 Mouse 7.0 pEC50 = 7.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL441929 213902 0 None - 0 Mouse 6.0 pEC50 = 6.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL414711 213148 0 None - 0 Mouse 7.0 pEC50 = 7.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
CHEMBL410347 212813 0 None - 0 Mouse 7.0 pEC50 = 7.0 Binding
In vitro effective concentration for mouse corticotropin releasing factor 1 receptorIn vitro effective concentration for mouse corticotropin releasing factor 1 receptor
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1021/jm049490m
44596586 198776 0 None - 0 Rat 9.7 pIC50 = 9.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 398 7 1 6 4.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
CHEMBL583153 198776 0 None - 0 Rat 9.7 pIC50 = 9.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 398 7 1 6 4.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
44596589 198164 3 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 414 8 1 7 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
CHEMBL574852 198164 3 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 414 8 1 7 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
44596589 198164 3 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 414 8 1 7 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL574852 198164 3 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 414 8 1 7 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.01.129
44194976 195934 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 377 7 1 6 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL559437 195934 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 377 7 1 6 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
44194976 195934 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 377 7 1 6 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL559437 195934 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 377 7 1 6 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
44194976 195934 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 377 7 1 6 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900302q
CHEMBL559437 195934 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 377 7 1 6 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900302q
44190059 195249 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 6 1 5 4.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL551033 195249 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 6 1 5 4.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
44596809 198891 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 362 6 1 6 4.0 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
CHEMBL584343 198891 0 None - 0 Rat 9.6 pIC50 = 9.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 362 6 1 6 4.0 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
44596589 198164 3 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 414 8 1 7 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
CHEMBL574852 198164 3 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 414 8 1 7 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
44190148 196006 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 377 7 1 6 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL560036 196006 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 377 7 1 6 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
44596812 198804 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 384 6 1 6 4.2 Cc1cc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)nc1OC(F)F 10.1021/jm900716v
CHEMBL583387 198804 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 384 6 1 6 4.2 Cc1cc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)nc1OC(F)F 10.1021/jm900716v
44596812 198804 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 384 6 1 6 4.2 Cc1cc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)nc1OC(F)F 10.1016/j.bmcl.2010.01.129
CHEMBL583387 198804 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 384 6 1 6 4.2 Cc1cc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)nc1OC(F)F 10.1016/j.bmcl.2010.01.129
11420978 11764 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 402 7 1 5 4.8 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1Cl 10.1021/jm049737f
CHEMBL1181645 11764 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 402 7 1 5 4.8 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1Cl 10.1021/jm049737f
CHEMBL187073 11764 0 None - 0 Rat 9.5 pIC50 = 9.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 402 7 1 5 4.8 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1Cl 10.1021/jm049737f
44190143 194841 0 None - 0 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 347 5 1 5 4.2 COc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900301y
CHEMBL539670 194841 0 None - 0 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 347 5 1 5 4.2 COc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900301y
44190143 194841 0 None - 0 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 347 5 1 5 4.2 COc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900302q
CHEMBL539670 194841 0 None - 0 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 347 5 1 5 4.2 COc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900302q
44190915 196004 0 None - 0 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 401 6 1 5 5.3 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL560033 196004 0 None - 0 Rat 9.4 pIC50 = 9.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 401 6 1 5 5.3 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1021/jm900302q
71580213 88432 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 409 9 1 6 4.2 COc1cc(C)c(Nc2nc(Cl)cn([C@@H](COCCF)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2013.02.009
CHEMBL2349558 88432 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 409 9 1 6 4.2 COc1cc(C)c(Nc2nc(Cl)cn([C@@H](COCCF)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2013.02.009
71580215 88434 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 493 9 1 6 5.0 COc1cc(Cl)c(Nc2nc(Br)cn([C@@H](COCCF)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2013.02.009
CHEMBL2349560 88434 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 493 9 1 6 5.0 COc1cc(Cl)c(Nc2nc(Br)cn([C@@H](COCCF)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2013.02.009
44190828 196309 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 423 6 1 5 5.5 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL562218 196309 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 423 6 1 5 5.5 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1021/jm900302q
11384238 66850 0 None - 1 Rat 9.3 pIC50 = 9.3 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 406 6 1 4 5.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl 10.1021/jm049737f
CHEMBL186203 66850 0 None - 1 Rat 9.3 pIC50 = 9.3 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 406 6 1 4 5.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl 10.1021/jm049737f
44596588 197864 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 414 8 1 7 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
CHEMBL572589 197864 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 414 8 1 7 3.9 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
9931946 11770 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 420 7 1 5 4.9 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1cc(F)c(OC)cc1Cl 10.1021/jm049737f
CHEMBL1181679 11770 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 420 7 1 5 4.9 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1cc(F)c(OC)cc1Cl 10.1021/jm049737f
CHEMBL188464 11770 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 420 7 1 5 4.9 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1cc(F)c(OC)cc1Cl 10.1021/jm049737f
45266992 196076 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 6 1 5 4.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL560634 196076 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 6 1 5 4.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(OC)cc2C)c1=O 10.1021/jm900301y
44190242 195209 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 385 5 1 4 5.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(Cl)cc2Cl)c1=O 10.1021/jm900301y
CHEMBL550686 195209 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 385 5 1 4 5.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(Cl)cc2Cl)c1=O 10.1021/jm900301y
44190242 195209 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 385 5 1 4 5.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(Cl)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL550686 195209 0 None - 0 Rat 9.3 pIC50 = 9.3 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 385 5 1 4 5.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(Cl)cc2Cl)c1=O 10.1021/jm900302q
44190144 195465 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 365 7 1 6 3.9 CC[C@H](COC)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL552504 195465 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 365 7 1 6 3.9 CC[C@H](COC)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
71580214 88433 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 449 9 1 6 4.9 COc1cc(Cl)c(Nc2nc(Cl)cn([C@@H](COCCF)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2013.02.009
CHEMBL2349559 88433 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 449 9 1 6 4.9 COc1cc(Cl)c(Nc2nc(Cl)cn([C@@H](COCCF)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2013.02.009
71580426 88443 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 345 6 1 5 3.8 COc1cc(C)c(Nc2nc(C)cn([C@@H](CF)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2013.02.009
CHEMBL2349570 88443 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 345 6 1 5 3.8 COc1cc(C)c(Nc2nc(C)cn([C@@H](CF)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2013.02.009
44190058 196044 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 377 8 1 5 5.4 CCCC(CCC)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL560350 196044 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 377 8 1 5 5.4 CCCC(CCC)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
44190446 196678 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 379 4 0 5 4.2 COc1cc(Cl)c2c(c1)CCN2c1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900301y
CHEMBL564588 196678 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 379 4 0 5 4.2 COc1cc(Cl)c2c(c1)CCN2c1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900301y
44189950 196509 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 345 5 1 4 4.9 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL563489 196509 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 345 5 1 4 4.9 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
44189950 196509 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 345 5 1 4 4.9 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900302q
CHEMBL563489 196509 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 345 5 1 4 4.9 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900302q
56961965 81997 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 425 8 1 7 3.2 COCC(COC)n1cc(Br)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL2165202 81997 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 425 8 1 7 3.2 COCC(COC)n1cc(Br)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
46881748 6925 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 5 1 6 3.7 Cc1cc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)nc1N(C)C 10.1016/j.bmcl.2010.01.129
CHEMBL1084423 6925 0 None - 0 Rat 9.2 pIC50 = 9.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 5 1 6 3.7 Cc1cc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)nc1N(C)C 10.1016/j.bmcl.2010.01.129
10027220 66865 0 None - 1 Rat 9.2 pIC50 = 9.2 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 458 7 1 4 6.0 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1021/jm049737f
CHEMBL186252 66865 0 None - 1 Rat 9.2 pIC50 = 9.2 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 458 7 1 4 6.0 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1021/jm049737f
44610627 139975 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 519 9 2 8 5.5 Cc1cc(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccccc3)C3CC3)c2=O)c(C)nc1OC(F)F 10.1016/j.bmcl.2016.03.067
CHEMBL3799870 139975 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 519 9 2 8 5.5 Cc1cc(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccccc3)C3CC3)c2=O)c(C)nc1OC(F)F 10.1016/j.bmcl.2016.03.067
46881834 7742 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 400 8 1 7 3.5 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2ccc(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1089036 7742 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 400 8 1 7 3.5 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2ccc(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.01.129
44190057 195548 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 349 6 1 5 4.6 CCC(CC)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL554517 195548 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 349 6 1 5 4.6 CCC(CC)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
45483573 198165 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 395 6 1 7 3.8 Cc1nc(OC(F)F)c(C#N)cc1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900716v
CHEMBL574853 198165 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 395 6 1 7 3.8 Cc1nc(OC(F)F)c(C#N)cc1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900716v
10363553 66826 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 399 8 1 7 3.5 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1OC 10.1021/jm0611410
CHEMBL186097 66826 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 399 8 1 7 3.5 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1OC 10.1021/jm0611410
10363553 66826 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 399 8 1 7 3.5 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1OC 10.1021/jm049737f
CHEMBL186097 66826 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 399 8 1 7 3.5 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1OC 10.1021/jm049737f
45483574 198034 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 425 8 1 8 3.4 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C#N)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
CHEMBL573978 198034 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 425 8 1 8 3.4 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C#N)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
44190145 195208 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 351 6 1 6 3.5 COC[C@@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL550685 195208 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 351 6 1 6 3.5 COC[C@@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
46891155 7236 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 342 6 1 6 3.7 CCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1085753 7236 0 None - 0 Rat 9.1 pIC50 = 9.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 342 6 1 6 3.7 CCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1016/j.bmcl.2010.04.121
44191013 196248 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 391 4 1 4 5.6 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL561758 196248 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 391 4 1 4 5.6 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1=O 10.1021/jm900302q
11752878 12263 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 414 7 1 4 5.9 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
CHEMBL1184703 12263 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 414 7 1 4 5.9 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
CHEMBL364883 12263 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 414 7 1 4 5.9 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
11417694 67453 0 None - 1 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 382 7 1 5 4.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1021/jm0611410
CHEMBL189089 67453 0 None - 1 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 382 7 1 5 4.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1021/jm0611410
11417694 67453 0 None - 1 Rat 9.0 pIC50 = 9.0 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 382 7 1 5 4.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1021/jm049737f
CHEMBL189089 67453 0 None - 1 Rat 9.0 pIC50 = 9.0 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 382 7 1 5 4.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1021/jm049737f
44190447 196304 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 423 4 0 5 4.3 COc1cc(Br)c2c(c1)CCN2c1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900301y
CHEMBL562161 196304 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 423 4 0 5 4.3 COc1cc(Br)c2c(c1)CCN2c1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900301y
44191012 196236 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 351 4 1 4 4.9 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(Cl)c1 10.1021/jm900302q
CHEMBL561698 196236 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 351 4 1 4 4.9 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(Cl)c1 10.1021/jm900302q
42618183 179813 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 393 8 0 7 3.9 C=CCN(CC=C)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL474498 179813 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 393 8 0 7 3.9 C=CCN(CC=C)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
42618197 184306 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 391 6 1 6 4.8 CCC(CC)Nc1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
CHEMBL484158 184306 0 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 391 6 1 6 4.8 CCC(CC)Nc1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
44194975 196310 16 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 423 6 1 5 5.5 C[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL562219 196310 16 None - 0 Rat 9.0 pIC50 = 9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 423 6 1 5 5.5 C[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1021/jm900302q
71580425 88442 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 365 6 1 5 4.2 COc1cc(C)c(Nc2nc(Cl)cn([C@@H](CF)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2013.02.009
CHEMBL2349569 88442 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 365 6 1 5 4.2 COc1cc(C)c(Nc2nc(Cl)cn([C@@H](CF)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2013.02.009
44596808 198240 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 378 7 1 7 3.3 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
CHEMBL575491 198240 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 378 7 1 7 3.3 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
46891337 6410 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 395 8 1 8 2.9 COCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1082349 6410 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 395 8 1 8 2.9 COCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
46891439 7067 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 395 8 1 8 2.9 COC[C@@H](C1CC1)n1nc(C)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1084987 7067 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 395 8 1 8 2.9 COC[C@@H](C1CC1)n1nc(C)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
44190826 194820 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 387 5 1 5 4.9 COc1cc(Cl)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(Cl)c1 10.1021/jm900301y
CHEMBL539184 194820 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 387 5 1 5 4.9 COc1cc(Cl)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(Cl)c1 10.1021/jm900301y
44190826 194820 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 387 5 1 5 4.9 COc1cc(Cl)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(Cl)c1 10.1021/jm900302q
CHEMBL539184 194820 0 None - 0 Rat 9.0 pIC50 = 9.0 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 387 5 1 5 4.9 COc1cc(Cl)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(Cl)c1 10.1021/jm900302q
42618199 184164 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 437 9 0 8 3.3 COCCN(CCOC)c1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
CHEMBL482982 184164 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 437 9 0 8 3.3 COCCN(CCOC)c1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
42618197 184306 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 391 6 1 6 4.8 CCC(CC)Nc1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
CHEMBL484158 184306 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 391 6 1 6 4.8 CCC(CC)Nc1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
3499 1448 28 None - 1 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.bmcl.2016.03.067
9909468 1448 28 None - 1 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.bmcl.2016.03.067
CHEMBL44698 1448 28 None - 1 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.bmcl.2016.03.067
127047546 139658 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 441 8 1 8 4.1 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3ccccn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3797830 139658 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 441 8 1 8 4.1 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3ccccn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
46881792 7334 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 402 5 1 6 4.3 COc1nc(C(F)(F)F)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.01.129
CHEMBL1086179 7334 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 402 5 1 6 4.3 COc1nc(C(F)(F)F)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.01.129
46881793 7336 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 370 6 1 6 3.9 Cc1nc(OC(F)F)ccc1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1086180 7336 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 370 6 1 6 3.9 Cc1nc(OC(F)F)ccc1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1016/j.bmcl.2010.01.129
46881835 7743 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 400 8 1 7 3.5 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2ccc(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1089037 7743 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 400 8 1 7 3.5 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2ccc(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.01.129
44190149 195060 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 396 5 1 5 5.2 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900301y
CHEMBL549538 195060 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 396 5 1 5 5.2 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900301y
44190450 195658 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 432 5 1 6 4.1 COc1ccc(Nc2nc(Br)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
CHEMBL556462 195658 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 432 5 1 6 4.1 COc1ccc(Nc2nc(Br)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
CHEMBL1077301 208491 0 None - 2 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CO)[C@@H](C)CC)[C@@H](C)O)C(C)C)[C@@H](C)O)C(=O)N[C@@H](C)C(N)=O 10.1016/j.bmcl.2010.01.129
42618181 184358 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 369 6 0 7 3.6 CCN(CC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL484420 184358 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 369 6 0 7 3.6 CCN(CC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
3499 1448 28 None - 1 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm900302q
9909468 1448 28 None - 1 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm900302q
CHEMBL44698 1448 28 None - 1 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm900302q
44190149 195060 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 396 5 1 5 5.2 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL549538 195060 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 396 5 1 5 5.2 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900302q
44190829 195301 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 371 4 1 4 5.2 Cc1cc(Cl)cc(Cl)c1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900302q
CHEMBL551433 195301 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 371 4 1 4 5.2 Cc1cc(Cl)cc(Cl)c1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900302q
44190913 195945 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 361 6 1 5 4.6 CCOc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900302q
CHEMBL559507 195945 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 361 6 1 5 4.6 CCOc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900302q
11246513 66860 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 397 6 1 5 4.6 CCCN(CCC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1Cl 10.1021/jm049737f
CHEMBL186241 66860 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 397 6 1 5 4.6 CCCN(CCC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1Cl 10.1021/jm049737f
CHEMBL526149 215675 10 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL None None None CSCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(=O)O)[C@@H](C)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(N)=O 10.1021/jm9000242
44629380 139886 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 508 8 2 9 4.7 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3cccc(C#N)c3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3799337 139886 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 508 8 2 9 4.7 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3cccc(C#N)c3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
44189947 195100 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 6 1 5 4.2 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL549875 195100 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 6 1 5 4.2 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
44191008 196257 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 439 5 1 4 6.3 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL561819 196257 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 439 5 1 4 6.3 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
45483576 198365 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 425 8 1 8 3.4 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C#N)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
CHEMBL576589 198365 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 425 8 1 8 3.4 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C#N)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
44189951 195027 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 349 6 1 5 4.2 CC[C@H](COC)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL549329 195027 0 None - 0 Rat 8.9 pIC50 = 8.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 349 6 1 5 4.2 CC[C@H](COC)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
44591500 189732 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 395 7 0 7 4.1 CCCN(c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12)C1CC1 10.1021/jm9000242
CHEMBL515740 189732 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 395 7 0 7 4.1 CCCN(c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12)C1CC1 10.1021/jm9000242
44596810 198002 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 348 5 1 6 3.6 COc1nc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900716v
CHEMBL573748 198002 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 348 5 1 6 3.6 COc1nc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900716v
44596807 198097 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 378 7 1 7 3.3 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
CHEMBL574436 198097 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 378 7 1 7 3.3 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
44629379 139685 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 517 8 2 8 5.5 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccccc3Cl)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3797992 139685 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 517 8 2 8 5.5 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccccc3Cl)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
44629309 139819 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 483 8 2 8 4.9 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccccc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3798885 139819 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 483 8 2 8 4.9 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccccc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
127047519 139908 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 468 8 1 8 4.5 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)c3ccccc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3799452 139908 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 468 8 1 8 4.5 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)c3ccccc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
127047547 140077 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 519 8 1 8 4.8 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3cc(Br)ccn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3800497 140077 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 519 8 1 8 4.8 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3cc(Br)ccn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
44596807 198097 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 378 7 1 7 3.3 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
CHEMBL574436 198097 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 378 7 1 7 3.3 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
44190340 195470 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 373 6 0 4 5.3 CC[C@H](C1CC1)n1cc(Cl)nc(N(CC)c2cc(C)c(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL552559 195470 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 373 6 0 4 5.3 CC[C@H](C1CC1)n1cc(Cl)nc(N(CC)c2cc(C)c(C)cc2C)c1=O 10.1021/jm900301y
44190337 196133 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 391 8 1 6 4.3 CCOc1cc(C)c(Nc2nc(Cl)cn([C@@H](COC)C3CC3)c2=O)cc1C 10.1021/jm900301y
CHEMBL561097 196133 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 391 8 1 6 4.3 CCOc1cc(C)c(Nc2nc(Cl)cn([C@@H](COC)C3CC3)c2=O)cc1C 10.1021/jm900301y
44596810 198002 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 348 5 1 6 3.6 COc1nc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.01.129
CHEMBL573748 198002 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 348 5 1 6 3.6 COc1nc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.01.129
11211931 124343 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 406 5 1 5 4.5 CCN(c1cc(C)nc2c1NC(=O)CN2c1cc(F)c(OC)cc1Cl)C(C)C 10.1021/jm049737f
CHEMBL363654 124343 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 406 5 1 5 4.5 CCN(c1cc(C)nc2c1NC(=O)CN2c1cc(F)c(OC)cc1Cl)C(C)C 10.1021/jm049737f
54582097 61039 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 372 7 0 7 3.3 CCN(CCCF)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1016/j.bmcl.2011.02.050
CHEMBL1762820 61039 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 372 7 0 7 3.3 CCN(CCCF)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1016/j.bmcl.2011.02.050
44596587 197863 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 388 7 1 7 3.5 COC[C@@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
CHEMBL572588 197863 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 388 7 1 7 3.5 COC[C@@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1021/jm900716v
127047548 139686 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 509 8 1 8 5.1 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3ccc(C(F)(F)F)cn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3798004 139686 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 509 8 1 8 5.1 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3ccc(C(F)(F)F)cn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
44629378 139834 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 517 8 2 8 5.5 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccc(Cl)cc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3799036 139834 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 517 8 2 8 5.5 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccc(Cl)cc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
44190449 195977 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 388 5 1 6 4.0 COc1ccc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.01.129
CHEMBL559764 195977 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 388 5 1 6 4.0 COc1ccc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.01.129
42618230 191338 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 380 7 0 7 3.7 CCCN(CC1CC1)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL519159 191338 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 380 7 0 7 3.7 CCCN(CC1CC1)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
44191010 195147 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 455 6 1 5 5.6 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL550216 195147 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 455 6 1 5 5.6 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
42618198 184163 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 377 5 0 6 4.1 CCN(CC)c1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
CHEMBL482981 184163 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 377 5 0 6 4.1 CCN(CC)c1nc(C)nc2c(-c3cc(F)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
44596701 198033 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 353 6 1 7 3.2 CC[C@H](C1CC1)n1cc(C#N)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
CHEMBL573976 198033 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 353 6 1 7 3.2 CC[C@H](C1CC1)n1cc(C#N)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
44629377 139965 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 551 8 2 8 6.2 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3cc(Cl)cc(Cl)c3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3799825 139965 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 551 8 2 8 6.2 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3cc(Cl)cc(Cl)c3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
44629312 140061 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 551 8 2 8 6.2 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccc(Cl)cc3Cl)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3800413 140061 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 551 8 2 8 6.2 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3ccc(Cl)cc3Cl)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
44190145 195208 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 351 6 1 6 3.5 COC[C@@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL550685 195208 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 351 6 1 6 3.5 COC[C@@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
44189946 195828 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 331 4 1 4 4.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)c1 10.1016/j.bmcl.2010.01.129
44189946 195828 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 331 4 1 4 4.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)c1 10.1021/jm900301y
CHEMBL558280 195828 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 331 4 1 4 4.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)c1 10.1016/j.bmcl.2010.01.129
CHEMBL558280 195828 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 331 4 1 4 4.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)c1 10.1021/jm900301y
44189946 195828 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 331 4 1 4 4.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)c1 10.1021/jm900302q
CHEMBL558280 195828 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 331 4 1 4 4.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)c1 10.1021/jm900302q
44190918 196005 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 400 6 1 6 4.4 CC[C@H](COC)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL560034 196005 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 400 6 1 6 4.4 CC[C@H](COC)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900302q
42618187 180164 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 397 8 0 7 4.4 CCCCN(CC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL474901 180164 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 397 8 0 7 4.4 CCCCN(CC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
42618188 179278 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 399 8 0 8 3.2 CCN(CCOC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL473075 179278 0 None - 0 Rat 8.8 pIC50 = 8.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 399 8 0 8 3.2 CCN(CCOC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
44190449 195977 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 388 5 1 6 4.0 COc1ccc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
CHEMBL559764 195977 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 388 5 1 6 4.0 COc1ccc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
42618189 189690 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 425 9 0 8 3.6 COCCN(CC1CC1)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL515396 189690 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 425 9 0 8 3.6 COCCN(CC1CC1)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
44190823 196197 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 455 6 1 5 6.2 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL561416 196197 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 455 6 1 5 6.2 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
11154464 67470 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 423 6 1 5 5.0 CCCN(CC1CCC1)c1cc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1Cl 10.1021/jm049737f
CHEMBL189196 67470 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 423 6 1 5 5.0 CCCN(CC1CCC1)c1cc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1Cl 10.1021/jm049737f
42618172 179998 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 376 6 0 7 3.6 COc1ccc(-c2c(C)nn3c(N(CCC#N)C4CC4)nc(C)nc23)c(C)c1 10.1021/jm9000242
CHEMBL474701 179998 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 376 6 0 7 3.6 COc1ccc(-c2c(C)nn3c(N(CCC#N)C4CC4)nc(C)nc23)c(C)c1 10.1021/jm9000242
52918270 61040 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 402 9 0 8 2.9 COCCN(CCCF)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1016/j.bmcl.2011.02.050
CHEMBL1762821 61040 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 402 9 0 8 2.9 COCCN(CCCF)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1016/j.bmcl.2011.02.050
44629381 139960 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 520 9 2 9 4.8 Cc1cc(Nc2nc(Cl)cn([C@H](COC(=O)Nc3cccnc3)C3CC3)c2=O)c(C)nc1OC(F)F 10.1016/j.bmcl.2016.03.067
CHEMBL3799784 139960 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 520 9 2 9 4.8 Cc1cc(Nc2nc(Cl)cn([C@H](COC(=O)Nc3cccnc3)C3CC3)c2=O)c(C)nc1OC(F)F 10.1016/j.bmcl.2016.03.067
42618196 191473 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 371 6 1 6 4.5 CCC(CC)Nc1nc(C)nc2c(-c3cc(F)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL519340 191473 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 371 6 1 6 4.5 CCC(CC)Nc1nc(C)nc2c(-c3cc(F)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
42618170 180839 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 379 7 0 6 4.4 CCCN(CC1CC1)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL475706 180839 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 379 7 0 6 4.4 CCCN(CC1CC1)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
42618195 184286 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 413 9 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c(-c3cc(C)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL483993 184286 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 413 9 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c(-c3cc(C)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
21984762 77542 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 409 8 0 4 5.9 CCc1nn2c(-c3ccc(OC)cc3Cl)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087550 77542 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 409 8 0 4 5.9 CCc1nn2c(-c3ccc(OC)cc3Cl)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
44596702 197947 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 339 5 1 7 2.9 COc1nc(C)c(Nc2nc(C#N)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900716v
CHEMBL573284 197947 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 339 5 1 7 2.9 COc1nc(C)c(Nc2nc(C#N)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900716v
46891188 6644 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 397 4 1 6 4.5 Cc1nc(Nc2c(Cl)cc(C#N)c(Cl)c2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1083343 6644 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 397 4 1 6 4.5 Cc1nc(Nc2c(Cl)cc(C#N)c(Cl)c2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
44629310 139898 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 484 8 2 9 4.3 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3cccnc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3799417 139898 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 484 8 2 9 4.3 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)Nc3cccnc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
58280026 140082 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 449 9 2 8 3.7 CCCNC(=O)OC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
CHEMBL3800523 140082 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 449 9 2 8 3.7 CCCNC(=O)OC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
44190147 196744 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 363 6 2 6 3.2 COc1cc(C)c(Nc2nc(Cl)cn([C@@H](CO)C3CC3)c2=O)cc1C 10.1021/jm900301y
CHEMBL565169 196744 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 363 6 2 6 3.2 COc1cc(C)c(Nc2nc(Cl)cn([C@@H](CO)C3CC3)c2=O)cc1C 10.1021/jm900301y
24768326 97776 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 328 6 0 4 5.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)nc2C)c1C 10.1021/jm070578k
CHEMBL271762 97776 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 328 6 0 4 5.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)nc2C)c1C 10.1021/jm070578k
10295702 122900 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 420 6 0 4 5.7 CCCC(C1CC1)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL360589 122900 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 420 6 0 4 5.7 CCCC(C1CC1)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
11306819 12408 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 397 6 1 5 4.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1C#N 10.1021/jm049737f
CHEMBL1185802 12408 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 397 6 1 5 4.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1C#N 10.1021/jm049737f
CHEMBL433592 12408 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 397 6 1 5 4.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1C#N 10.1021/jm049737f
24768326 97776 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 328 6 0 4 5.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)nc2C)c1C 10.1021/jm070578k
CHEMBL271762 97776 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 328 6 0 4 5.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)nc2C)c1C 10.1021/jm070578k
9927970 97736 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
CHEMBL271558 97736 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
9819482 157547 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 0 4 5.2 CCC(COC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL408028 157547 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 0 4 5.2 CCC(COC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
70692631 75900 0 None - 0 Human 7.0 pIC50 = 7 Binding
Binding affinity to CRF1 receptor (unknown origin)Binding affinity to CRF1 receptor (unknown origin)
ChEMBL 378 7 2 4 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)[nH]c12 10.1016/j.ejmech.2021.114085
CHEMBL2049190 75900 0 None - 0 Human 7.0 pIC50 = 7 Binding
Binding affinity to CRF1 receptor (unknown origin)Binding affinity to CRF1 receptor (unknown origin)
ChEMBL 378 7 2 4 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)[nH]c12 10.1016/j.ejmech.2021.114085
70692631 75900 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 378 7 2 4 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)[nH]c12 10.1016/j.bmcl.2012.05.066
CHEMBL2049190 75900 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 378 7 2 4 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)[nH]c12 10.1016/j.bmcl.2012.05.066
17961227 94407 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 483 6 0 3 8.2 CCCC(CCC)n1cc2c3c(nc(C)cc31)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL250982 94407 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 483 6 0 3 8.2 CCCC(CCC)n1cc2c3c(nc(C)cc31)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1016/j.bmcl.2007.06.077
44589204 189501 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 384 3 0 7 4.3 Cc1cc(C#N)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
CHEMBL513967 189501 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 384 3 0 7 4.3 Cc1cc(C#N)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
21912321 97779 0 None - 0 Rat 7.0 pIC50 = 7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 4 0 4 4.6 Cc1cc(C)c(Oc2nc(C)cc(OC3CCOC3)c2C)c(C)c1 10.1021/jm070578k
CHEMBL271770 97779 0 None - 0 Rat 7.0 pIC50 = 7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 4 0 4 4.6 Cc1cc(C)c(Oc2nc(C)cc(OC3CCOC3)c2C)c(C)c1 10.1021/jm070578k
57785838 165105 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 503 6 0 6 6.3 CCc1nc(C)nc(CC)c1N1CCCn2c1nc1c(Cl)ccc(C(OC(F)F)C(F)(F)F)c12 10.1016/j.bmc.2018.01.020
CHEMBL4227282 165105 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 503 6 0 6 6.3 CCc1nc(C)nc(CC)c1N1CCCn2c1nc1c(Cl)ccc(C(OC(F)F)C(F)(F)F)c12 10.1016/j.bmc.2018.01.020
11122528 65228 0 None - 1 Human 6.0 pIC50 = 6 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 413 10 0 7 4.0 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(OC)cc(OC)cc2OC)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL182643 65228 0 None - 1 Human 6.0 pIC50 = 6 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 413 10 0 7 4.0 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(OC)cc(OC)cc2OC)c1C 10.1016/j.bmcl.2004.05.072
58223462 128810 0 None - 0 Human 7.0 pIC50 = 7 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 473 10 0 9 4.7 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(C=O)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3669429 128810 0 None - 0 Human 7.0 pIC50 = 7 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 473 10 0 9 4.7 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(C=O)cc3OC)csc12)C1CCOCC1 nan
57912458 82606 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 487 10 0 9 4.6 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)C4CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179184 82606 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 487 10 0 9 4.6 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)C4CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
71458703 81515 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 419 8 0 6 5.1 CCN(CC)c1ccc(C#N)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160164 81515 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 419 8 0 6 5.1 CCN(CC)c1ccc(C#N)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
24768342 85578 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 364 6 1 6 4.2 CCCCN(CC)c1nc(C)nc2c1NCCN2c1ccc(C#N)cc1C 10.1021/jm0611410
CHEMBL228130 85578 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 364 6 1 6 4.2 CCCCN(CC)c1nc(C)nc2c1NCCN2c1ccc(C#N)cc1C 10.1021/jm0611410
21912321 97779 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 4 0 4 4.6 Cc1cc(C)c(Oc2nc(C)cc(OC3CCOC3)c2C)c(C)c1 10.1021/jm070578k
CHEMBL271770 97779 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 4 0 4 4.6 Cc1cc(C)c(Oc2nc(C)cc(OC3CCOC3)c2C)c(C)c1 10.1021/jm070578k
71462234 81522 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 452 11 0 6 6.0 CCCN(CCC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160171 81522 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 452 11 0 6 6.0 CCCN(CCC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
60155794 77562 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 449 9 0 6 5.2 CCc1nn2c(-c3c(OC)cccc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087570 77562 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 449 9 0 6 5.2 CCc1nn2c(-c3c(OC)cccc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
71458705 81521 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 438 10 0 6 5.5 CCc1cc2c(N(CC)CC)ccc(OC)c2nc1-c1c(OC)cc(COC)cc1OC 10.1016/j.bmc.2012.09.028
CHEMBL2160170 81521 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 438 10 0 6 5.5 CCc1cc2c(N(CC)CC)ccc(OC)c2nc1-c1c(OC)cc(COC)cc1OC 10.1016/j.bmc.2012.09.028
44392550 64568 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 489 9 0 8 5.0 CCCC(CCC)n1c(CC)nc2c1c(=O)n(C)c(=O)n2-c1cc(-c2cccnc2)c(OC)cc1C 10.1021/jm049787k
CHEMBL181546 64568 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 489 9 0 8 5.0 CCCC(CCC)n1c(CC)nc2c1c(=O)n(C)c(=O)n2-c1cc(-c2cccnc2)c(OC)cc1C 10.1021/jm049787k
70690704 76614 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 438 10 0 6 5.2 CCN(CCOC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063375 76614 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 438 10 0 6 5.2 CCN(CCOC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
70690704 76614 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 438 10 0 6 5.2 CCN(CCOC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2063375 76614 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 438 10 0 6 5.2 CCN(CCOC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
21912293 97815 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 6 0 3 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cccc2C)c1C 10.1021/jm070578k
CHEMBL271974 97815 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 6 0 3 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cccc2C)c1C 10.1021/jm070578k
21912397 98036 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 8 0 4 6.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(OC(C)C)cc2C)c1C 10.1021/jm070578k
CHEMBL273033 98036 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 8 0 4 6.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(OC(C)C)cc2C)c1C 10.1021/jm070578k
58896510 139508 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 430 6 1 5 5.6 CCN(c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12)C(C)C 10.1021/acs.jmedchem.5b01715
CHEMBL3793568 139508 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 430 6 1 5 5.6 CCN(c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12)C(C)C 10.1021/acs.jmedchem.5b01715
CHEMBL3794598 139508 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 430 6 1 5 5.6 CCN(c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12)C(C)C 10.1021/acs.jmedchem.5b01715
46891088 7070 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 452 7 1 7 4.5 COCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1084997 7070 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 452 7 1 7 4.5 COCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
46891035 7403 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 436 6 1 6 4.6 COCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1086510 7403 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 436 6 1 6 4.6 COCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
46845695 6922 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 334 5 1 6 3.3 COc1ccc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)n1 10.1016/j.bmcl.2010.01.129
CHEMBL1084413 6922 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 334 5 1 6 3.3 COc1ccc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)n1 10.1016/j.bmcl.2010.01.129
44190917 196225 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 429 5 1 5 5.2 COC[C@@H](C)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL561615 196225 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 429 5 1 5 5.2 COC[C@@H](C)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
9927970 97736 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
CHEMBL271558 97736 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
9819482 157547 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 0 4 5.2 CCC(COC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL408028 157547 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 0 4 5.2 CCC(COC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
57785862 164941 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 388 4 0 4 5.7 CCN(CC)c1cccc2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4224887 164941 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 388 4 0 4 5.7 CCN(CC)c1cccc2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
3495 1175 28 None - 1 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2011.02.086
5311055 1175 28 None - 1 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2011.02.086
CHEMBL9946 1175 28 None - 1 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2011.02.086
42618206 180171 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 6 1 6 4.6 CCC(CC)Nc1nc(C)nc2c(-c3ccc(OC)c(C)c3C)c(C)nn12 10.1021/jm9000242
CHEMBL474907 180171 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 6 1 6 4.6 CCC(CC)Nc1nc(C)nc2c(-c3ccc(OC)c(C)c3C)c(C)nn12 10.1021/jm9000242
42618165 174535 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 385 9 0 8 2.5 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3)c(C)nn12 10.1021/jm9000242
CHEMBL455588 174535 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 385 9 0 8 2.5 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3)c(C)nn12 10.1021/jm9000242
24758072 69977 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 320 4 0 2 6.1 CCC(CC)c1cc(C)n2nc(-c3ccc(C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939572 69977 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 320 4 0 2 6.1 CCC(CC)c1cc(C)n2nc(-c3ccc(C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
24768331 85474 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 369 7 1 6 4.3 CCCCN(CC)c1nc(C)nc2c1NCCN2c1ccc(OC)cc1C 10.1021/jm0611410
CHEMBL226761 85474 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 369 7 1 6 4.3 CCCCN(CC)c1nc(C)nc2c1NCCN2c1ccc(OC)cc1C 10.1021/jm0611410
44362115 1169 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Compound was evaluated for affinity towards Corticotropin releasing factor receptor 1 expressing tissues such as Cortex, cerebellumCompound was evaluated for affinity towards Corticotropin releasing factor receptor 1 expressing tissues such as Cortex, cerebellum
ChEMBL None None None None 10.1021/jm0202122
6967 1169 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Compound was evaluated for affinity towards Corticotropin releasing factor receptor 1 expressing tissues such as Cortex, cerebellumCompound was evaluated for affinity towards Corticotropin releasing factor receptor 1 expressing tissues such as Cortex, cerebellum
ChEMBL None None None None 10.1021/jm0202122
CHEMBL1201609 1169 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Compound was evaluated for affinity towards Corticotropin releasing factor receptor 1 expressing tissues such as Cortex, cerebellumCompound was evaluated for affinity towards Corticotropin releasing factor receptor 1 expressing tissues such as Cortex, cerebellum
ChEMBL None None None None 10.1021/jm0202122
CHEMBL440057 1169 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Compound was evaluated for affinity towards Corticotropin releasing factor receptor 1 expressing tissues such as Cortex, cerebellumCompound was evaluated for affinity towards Corticotropin releasing factor receptor 1 expressing tissues such as Cortex, cerebellum
ChEMBL None None None None 10.1021/jm0202122
71456850 81516 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 424 9 0 6 5.2 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160166 81516 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 424 9 0 6 5.2 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
21912293 97815 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 6 0 3 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cccc2C)c1C 10.1021/jm070578k
CHEMBL271974 97815 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 6 0 3 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cccc2C)c1C 10.1021/jm070578k
21912397 98036 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 8 0 4 6.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(OC(C)C)cc2C)c1C 10.1021/jm070578k
CHEMBL273033 98036 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 8 0 4 6.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(OC(C)C)cc2C)c1C 10.1021/jm070578k
70909662 156228 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 448 6 1 5 6.1 CCC(=O)N(c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12)C(C)C 10.1016/j.bmc.2016.11.011
CHEMBL4064670 156228 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 448 6 1 5 6.1 CCC(=O)N(c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12)C(C)C 10.1016/j.bmc.2016.11.011
137654892 158625 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 420 7 2 5 6.5 CCC(CC)Nc1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4092351 158625 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 420 7 2 5 6.5 CCC(CC)Nc1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
44129684 165030 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4226158 165030 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
9951076 67411 2 None - 1 Human 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1021/jm040058e
CHEMBL188844 67411 2 None - 1 Human 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1021/jm040058e
CHEMBL2165204 67411 2 None - 1 Human 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1021/jm040058e
10616876 101358 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 336 5 1 4 5.2 CCCCNc1nc(C)nc2c1c(C)cn2-c1c(C)cc(C)cc1C 10.1021/jm960861b
CHEMBL296977 101358 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 336 5 1 4 5.2 CCCCNc1nc(C)nc2c1c(C)cn2-c1c(C)cc(C)cc1C 10.1021/jm960861b
46891338 7379 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 346 6 1 9 1.8 COc1nc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(OC)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1086374 7379 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 346 6 1 9 1.8 COc1nc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(OC)n1 10.1016/j.bmcl.2010.04.121
70888282 175137 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 556 7 1 7 6.3 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3ccc(S(C)(=O)=O)cc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4569860 175137 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 556 7 1 7 6.3 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3ccc(S(C)(=O)=O)cc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
54585865 60653 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 394 6 0 5 4.8 CCCN(CCC)c1nc2c(c(-c3c(C)cc(C)cc3C)c(C)n2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760257 60653 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 394 6 0 5 4.8 CCCN(CCC)c1nc2c(c(-c3c(C)cc(C)cc3C)c(C)n2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
57390211 69994 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 395 7 0 5 5.3 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC(C)C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939589 69994 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 395 7 0 5 5.3 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC(C)C)c(=O)c12 10.1016/j.bmc.2011.11.015
9800812 123636 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 394 5 0 4 5.3 CCc1nc2c(n1C(CC)CC)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL361912 123636 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 394 5 0 4 5.3 CCc1nc2c(n1C(CC)CC)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
56659877 65306 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 415 9 1 6 5.9 CCCN(CCC)c1c(C(C)C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828892 65306 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 415 9 1 6 5.9 CCCN(CCC)c1c(C(C)C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
60155990 77578 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 513 11 0 9 4.9 COCc1cc(OC)c(-c2cccc3c(N(CC4CC4)CC4OCCCO4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087800 77578 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 513 11 0 9 4.9 COCc1cc(OC)c(-c2cccc3c(N(CC4CC4)CC4OCCCO4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
10111759 64356 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 402 6 0 5 4.7 CCc1nc2c(n1C(CC)C1CC1)C(=O)N(C)CN2c1ccc(OC)cc1Cl 10.1021/jm049787k
CHEMBL181259 64356 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 402 6 0 5 4.7 CCc1nc2c(n1C(CC)C1CC1)C(=O)N(C)CN2c1ccc(OC)cc1Cl 10.1021/jm049787k
44589350 189602 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 387 3 0 7 3.7 N#Cc1ccc(N2CCc3c(-n4ccc(-n5cccn5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
CHEMBL514761 189602 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 387 3 0 7 3.7 N#Cc1ccc(N2CCc3c(-n4ccc(-n5cccn5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
70696935 76609 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 450 11 0 5 6.6 CCCN(CCC)c1ccc(CC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063370 76609 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 450 11 0 5 6.6 CCCN(CCC)c1ccc(CC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
58223504 127834 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 11 0 9 5.2 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)c(CC)sc12)C1CCOCC1 nan
CHEMBL3664547 127834 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 11 0 9 5.2 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)c(CC)sc12)C1CCOCC1 nan
71455052 81518 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 428 9 0 6 5.1 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160168 81518 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 428 9 0 6 5.1 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmc.2012.09.028
58896594 139504 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 444 8 1 5 6.0 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793367 139504 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 444 8 1 5 6.0 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794594 139504 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 444 8 1 5 6.0 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
56683763 65501 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
CHEMBL1830519 65501 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
21984648 77544 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 389 8 0 4 5.5 CCc1nn2c(-c3ccc(C)cc3OC)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087552 77544 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 389 8 0 4 5.5 CCc1nn2c(-c3ccc(C)cc3OC)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
44596700 198619 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 369 7 1 8 2.5 COC[C@H](C1CC1)n1cc(C#N)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
CHEMBL578838 198619 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 369 7 1 8 2.5 COC[C@H](C1CC1)n1cc(C#N)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
46891490 6468 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 369 5 1 7 3.1 COc1ccc(Nc2nc(C)nn([C@@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1082625 6468 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 369 5 1 7 3.1 COc1ccc(Nc2nc(C)nn([C@@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
46891233 6698 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 383 6 1 7 3.5 CCOc1ccc(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1083592 6698 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 383 6 1 7 3.5 CCOc1ccc(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
46845696 6389 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 348 5 1 6 3.6 COc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)n1 10.1016/j.bmcl.2010.01.129
CHEMBL1082241 6389 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 348 5 1 6 3.6 COc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)n1 10.1016/j.bmcl.2010.01.129
44190054 196013 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 335 5 1 5 3.8 COC[C@@H](C)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL560098 196013 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 335 5 1 5 3.8 COC[C@@H](C)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
42618225 179303 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 0 7 3.0 CCN(CC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL473276 179303 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 0 7 3.0 CCN(CC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
21912223 97585 1 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 328 6 1 4 5.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1N 10.1021/jm070578k
CHEMBL270780 97585 1 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 328 6 1 4 5.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1N 10.1021/jm070578k
21912419 98014 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 439 6 0 3 6.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(I)cc2C)c1C 10.1021/jm070578k
CHEMBL272912 98014 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 439 6 0 3 6.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(I)cc2C)c1C 10.1021/jm070578k
21912223 97585 1 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 328 6 1 4 5.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1N 10.1021/jm070578k
CHEMBL270780 97585 1 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 328 6 1 4 5.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1N 10.1021/jm070578k
21912419 98014 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 439 6 0 3 6.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(I)cc2C)c1C 10.1021/jm070578k
CHEMBL272912 98014 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 439 6 0 3 6.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(I)cc2C)c1C 10.1021/jm070578k
44444317 94061 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 363 5 0 4 5.7 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)cc1C)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL248962 94061 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 363 5 0 4 5.7 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)cc1C)CC2 10.1016/j.bmcl.2007.06.077
44444316 161674 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 358 4 0 4 5.6 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(C#N)cc1C)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL413134 161674 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 358 4 0 4 5.6 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(C#N)cc1C)CC2 10.1016/j.bmcl.2007.06.077
42618213 184093 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 409 8 0 7 4.5 CCCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL482543 184093 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 409 8 0 7 4.5 CCCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
58801644 77560 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(COC)cc(OC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087568 77560 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(COC)cc(OC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
58801647 77567 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 479 10 0 7 5.1 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087575 77567 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 479 10 0 7 5.1 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 10.1021/jm300259r
45268739 195955 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 365 4 1 5 4.3 C[C@H](C1CC1)n1cc(Cl)nc(Nc2cc3c(cc2Cl)COC3)c1=O 10.1021/jm900302q
CHEMBL559566 195955 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 365 4 1 5 4.3 C[C@H](C1CC1)n1cc(Cl)nc(Nc2cc3c(cc2Cl)COC3)c1=O 10.1021/jm900302q
155543377 173303 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 563 8 2 6 6.7 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(C(C)(C)C(N)=O)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4526083 173303 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 563 8 2 6 6.7 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(C(C)(C)C(N)=O)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
155568703 176113 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 521 7 2 6 6.0 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(C(N)=O)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4591720 176113 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 521 7 2 6 6.0 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(C(N)=O)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
11639510 60649 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 380 6 0 5 4.5 CCCN(CCC)c1nc2c(c(-c3c(C)cc(C)cc3C)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760253 60649 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 380 6 0 5 4.5 CCCN(CCC)c1nc2c(c(-c3c(C)cc(C)cc3C)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL5280146 194053 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition of human recombinant CRF1 in HEK cell line incubated for 2 hrs by MicroBeta scintillation counter methodInhibition of human recombinant CRF1 in HEK cell line incubated for 2 hrs by MicroBeta scintillation counter method
ChEMBL 382 4 0 5 5.5 CCN(CC)c1cc(C)nn2c(-c3sc4ccc(F)cc4c3C)c(C)nc12 10.1016/j.ejmech.2021.113867
11282792 189495 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 469 4 1 7 3.6 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(C#N)cc1OC(F)(F)F)CC2 10.1021/jm800744m
CHEMBL513937 189495 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 469 4 1 7 3.6 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(C#N)cc1OC(F)(F)F)CC2 10.1021/jm800744m
11338604 189687 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 402 4 1 7 3.1 COc1ccc(N2CCc3c(-n4ccc(-n5cc[nH]c5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL515363 189687 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 402 4 1 7 3.1 COc1ccc(N2CCc3c(-n4ccc(-n5cc[nH]c5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
45272175 195090 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 380 6 1 6 4.0 C=Cc1cn([C@H](C)C2CC2)c(=O)c(Nc2ccc(OC)nc2C(F)(F)F)n1 10.1021/jm900301y
CHEMBL549747 195090 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 380 6 1 6 4.0 C=Cc1cn([C@H](C)C2CC2)c(=O)c(Nc2ccc(OC)nc2C(F)(F)F)n1 10.1021/jm900301y
10474043 64577 0 None - 1 Human 5.9 pIC50 = 5.9 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 365 7 0 4 4.9 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL181593 64577 0 None - 1 Human 5.9 pIC50 = 5.9 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 365 7 0 4 4.9 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
57393712 69984 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 337 5 0 4 5.2 CCC(CC)c1nc(C)n2nc(-c3ccc(OC)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939579 69984 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 337 5 0 4 5.2 CCC(CC)c1nc(C)n2nc(-c3ccc(OC)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
9865886 175866 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 403 4 0 6 3.7 COc1ccc(N2CCc3c(-n4ccc(N5CCCC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL458599 175866 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 403 4 0 6 3.7 COc1ccc(N2CCc3c(-n4ccc(N5CCCC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
11189676 175589 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 432 5 1 6 3.9 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(OC(C)C)cc1C)CC2 10.1021/jm800744m
CHEMBL457975 175589 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 432 5 1 6 3.9 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(OC(C)C)cc1C)CC2 10.1021/jm800744m
44444331 94374 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 455 4 0 3 7.4 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL250803 94374 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 455 4 0 3 7.4 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1016/j.bmcl.2007.06.077
44444312 167775 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 391 7 0 4 6.5 CCCC(CCC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)cc1C)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL430396 167775 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 391 7 0 4 6.5 CCCC(CCC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)cc1C)CC2 10.1016/j.bmcl.2007.06.077
44589224 176027 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 398 4 0 7 4.5 CCc1cc(C#N)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
CHEMBL459007 176027 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 398 4 0 7 4.5 CCc1cc(C#N)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
71459110 82614 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 456 8 0 9 4.4 CCCN(c1c(OC)nn2c(-c3c(OC)cc(C#N)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179192 82614 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 456 8 0 9 4.4 CCCN(c1c(OC)nn2c(-c3c(OC)cc(C#N)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
53357535 130607 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 429 5 1 4 4.9 COc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
CHEMBL3681390 130607 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 429 5 1 4 4.9 COc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
11166718 67265 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 444 3 1 5 4.2 Cc1cc(N2CCOCC2)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2 10.1021/jm049737f
CHEMBL188112 67265 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 444 3 1 5 4.2 Cc1cc(N2CCOCC2)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2 10.1021/jm049737f
44589205 175958 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 425 4 0 8 4.6 Cc1cc(-n2cccn2)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
CHEMBL458826 175958 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 425 4 0 8 4.6 Cc1cc(-n2cccn2)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
127030924 139368 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 397 6 1 6 5.0 CCN(CC)c1ccc(C#N)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793070 139368 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 397 6 1 6 5.0 CCN(CC)c1ccc(C#N)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
127030927 139494 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 402 7 1 6 5.1 CCN(CC)c1ccc(OC)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794479 139494 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 402 7 1 6 5.1 CCN(CC)c1ccc(OC)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
58896493 139506 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 416 6 1 5 5.2 CCN(CC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793322 139506 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 416 6 1 5 5.2 CCN(CC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794596 139506 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 416 6 1 5 5.2 CCN(CC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
56673725 65309 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 403 9 1 7 4.8 CCCN(CCC)c1c(OC)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828895 65309 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 403 9 1 7 4.8 CCCN(CCC)c1c(OC)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
21984718 77546 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 403 8 0 4 5.8 CCc1nn2c(-c3c(C)cc(OC)cc3C)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087554 77546 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 403 8 0 4 5.8 CCc1nn2c(-c3c(C)cc(OC)cc3C)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
46891386 6411 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 404 6 1 6 4.6 Cc1nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c(=O)n([C@H](C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1082355 6411 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 404 6 1 6 4.6 Cc1nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c(=O)n([C@H](C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
46891191 6427 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 353 6 1 7 3.2 CCC(C1CC1)n1nc(C)nc(Nc2cc(OC)c(C#N)cc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1082402 6427 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 353 6 1 7 3.2 CCC(C1CC1)n1nc(C)nc(Nc2cc(OC)c(C#N)cc2C)c1=O 10.1016/j.bmcl.2010.04.121
155561680 175689 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 434 6 1 5 6.8 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3ccccc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4581950 175689 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 434 6 1 5 6.8 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3ccccc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
53357921 130612 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 427 5 1 3 5.4 CCc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
CHEMBL3681395 130612 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 427 5 1 3 5.4 CCc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
57398972 70008 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 339 3 0 5 3.8 COc1cc(C)c(-c2nn3c(C)cc(C(C)C)c3c(=O)n2C)c(C)c1 10.1016/j.bmc.2011.11.015
CHEMBL1939602 70008 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 339 3 0 5 3.8 COc1cc(C)c(-c2nn3c(C)cc(C(C)C)c3c(=O)n2C)c(C)c1 10.1016/j.bmc.2011.11.015
24758073 69979 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 364 7 0 3 6.5 CCOc1ccc(-c2nn3c(C)cc(C(CC)CC)c3cc2C)c(CC)c1 10.1016/j.bmc.2011.11.015
CHEMBL1939574 69979 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 364 7 0 3 6.5 CCOc1ccc(-c2nn3c(C)cc(C(CC)CC)c3cc2C)c(CC)c1 10.1016/j.bmc.2011.11.015
42618204 179280 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 429 10 0 9 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3cc(OC)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL473077 179280 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 429 10 0 9 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3cc(OC)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
42618214 192528 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 353 5 0 7 3.0 CCN(CC)c1nc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm900025h
CHEMBL520955 192528 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 353 5 0 7 3.0 CCN(CC)c1nc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm900025h
58223500 127851 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 10 0 9 5.0 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCOCC1 nan
CHEMBL3664564 127851 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 10 0 9 5.0 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCOCC1 nan
60155793 77557 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 479 10 0 7 5.2 CCc1nn2c(-c3cc(OC)c(OC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087565 77557 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 479 10 0 7 5.2 CCc1nn2c(-c3cc(OC)c(OC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
57785779 164931 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 459 4 0 5 6.7 CCC(c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl)n1ccnc1 10.1016/j.bmc.2018.01.020
CHEMBL4224722 164931 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 459 4 0 5 6.7 CCC(c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl)n1ccnc1 10.1016/j.bmc.2018.01.020
57393715 70004 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 339 3 0 6 2.9 Cc1nc(N(C)C)ccc1-c1nn2c(C)cc(C(C)C)c2c(=O)n1C 10.1016/j.bmc.2011.11.015
CHEMBL1939599 70004 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 339 3 0 6 2.9 Cc1nc(N(C)C)ccc1-c1nn2c(C)cc(C(C)C)c2c(=O)n1C 10.1016/j.bmc.2011.11.015
53358605 130594 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 422 5 1 4 5.2 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@@H](Cn2nc(-c3ccccc3)cc2C)CC1 nan
CHEMBL3681377 130594 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 422 5 1 4 5.2 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@@H](Cn2nc(-c3ccccc3)cc2C)CC1 nan
58223436 127839 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 445 9 0 9 3.8 CCCN(CC1CCOC1)c1c(OC)nn2c(-c3cnc(N(C)C)cc3OC)csc12 nan
CHEMBL3664552 127839 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 445 9 0 9 3.8 CCCN(CC1CCOC1)c1c(OC)nn2c(-c3cnc(N(C)C)cc3OC)csc12 nan
71451515 81509 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 405 7 0 6 5.0 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(C#N)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160158 81509 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 405 7 0 6 5.0 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(C#N)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
53357793 130609 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 399 4 1 3 4.9 Cc1cnn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1 nan
CHEMBL3681392 130609 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 399 4 1 3 4.9 Cc1cnn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1 nan
42618209 179809 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 427 9 0 9 2.6 COCCN(CCOC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL474492 179809 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 427 9 0 9 2.6 COCCN(CCOC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
53358858 130589 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 389 6 3 4 4.0 CCc1[nH]nc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)c1C nan
CHEMBL3681372 130589 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 389 6 3 4 4.0 CCc1[nH]nc(NC[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)c1C nan
21912226 97735 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 329 6 1 4 5.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(O)cc2C)c1C 10.1021/jm070578k
CHEMBL271557 97735 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 329 6 1 4 5.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(O)cc2C)c1C 10.1021/jm070578k
71453735 82611 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 475 9 0 9 4.6 COCc1cc(OC)c(-c2csc3c(N(C(C)C)C4CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179189 82611 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 475 9 0 9 4.6 COCc1cc(OC)c(-c2csc3c(N(C(C)C)C4CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
70696576 75583 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 438 11 0 6 6.1 CCCN(CCC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2046526 75583 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 438 11 0 6 6.1 CCCN(CCC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
70696576 75583 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 438 11 0 6 6.1 CCCN(CCC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2046526 75583 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 438 11 0 6 6.1 CCCN(CCC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
58896474 139444 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 400 8 1 5 5.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793985 139444 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 400 8 1 5 5.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
127031514 139452 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 425 8 1 6 5.8 CCCN(CCC)c1ccc(C#N)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794030 139452 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 425 8 1 6 5.8 CCCN(CCC)c1ccc(C#N)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
58896536 139507 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 472 10 1 5 6.8 CCCCN(CCCC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3792935 139507 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 472 10 1 5 6.8 CCCCN(CCCC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794597 139507 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 472 10 1 5 6.8 CCCCN(CCCC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
56677028 65299 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 359 7 2 6 4.7 CCC(CC)Nc1cc(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828886 65299 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 359 7 2 6 4.7 CCC(CC)Nc1cc(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
71580312 88437 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 475 9 1 8 3.4 COc1nc(Cl)nc(C)c1Nc1nc(Br)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
CHEMBL2349563 88437 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 475 9 1 8 3.4 COc1nc(Cl)nc(C)c1Nc1nc(Br)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
44596811 198243 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 352 6 1 7 2.9 COC[C@@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
CHEMBL575510 198243 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assayDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenate by binding titration assay
ChEMBL 352 6 1 7 2.9 COC[C@@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1021/jm900716v
46891033 7401 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 406 4 1 5 5.0 Cc1nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1086508 7401 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 406 4 1 5 5.0 Cc1nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
58280027 140004 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 435 8 2 8 3.4 CCNC(=O)OC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
CHEMBL3800035 140004 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 435 8 2 8 3.4 CCNC(=O)OC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
10179550 64879 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 406 5 0 4 5.3 CCc1nc2c(n1C(CC)C1CC1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL182169 64879 0 None - 0 Rat 7.9 pIC50 = 7.9 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 406 5 0 4 5.3 CCc1nc2c(n1C(CC)C1CC1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
136042278 69986 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 359 5 1 4 4.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)[nH]c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939581 69986 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 359 5 1 4 4.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)[nH]c(=O)c12 10.1016/j.bmc.2011.11.015
42618218 184133 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 0 7 3.0 CCN(CC)c1nc(C)nc2c(-c3cnc(OC)cc3C)c(C)nn12 10.1021/jm900025h
CHEMBL482751 184133 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 0 7 3.0 CCN(CC)c1nc(C)nc2c(-c3cnc(OC)cc3C)c(C)nn12 10.1021/jm900025h
42618211 179302 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 395 7 0 7 4.1 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL473275 179302 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 395 7 0 7 4.1 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
58896427 139503 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 1 4 5.6 CCCN(CCC)c1cccc2nc(Nc3c(C)cccc3C)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793329 139503 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 1 4 5.6 CCCN(CCC)c1cccc2nc(Nc3c(C)cccc3C)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794593 139503 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 1 4 5.6 CCCN(CCC)c1cccc2nc(Nc3c(C)cccc3C)n(C)c12 10.1021/acs.jmedchem.5b01715
46881864 8010 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 360 5 1 8 2.6 COc1nc(C)nc(C#N)c1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1090738 8010 0 None - 0 Rat 6.9 pIC50 = 6.9 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 360 5 1 8 2.6 COc1nc(C)nc(C#N)c1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1016/j.bmcl.2010.01.129
137646761 157840 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 479 7 2 6 4.4 CCN(CC(N)=O)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4083664 157840 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 479 7 2 6 4.4 CCN(CC(N)=O)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
54586828 60651 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 404 6 0 5 4.5 Cc1cc(C)c(-c2cn(C)c3nc(N(CC4CC4)CC4CC4)n(C)c(=O)c23)c(C)c1 10.1016/j.bmcl.2011.02.086
CHEMBL1760255 60651 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 404 6 0 5 4.5 Cc1cc(C)c(-c2cn(C)c3nc(N(CC4CC4)CC4CC4)n(C)c(=O)c23)c(C)c1 10.1016/j.bmcl.2011.02.086
21912226 97735 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 329 6 1 4 5.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(O)cc2C)c1C 10.1021/jm070578k
CHEMBL271557 97735 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 329 6 1 4 5.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(O)cc2C)c1C 10.1021/jm070578k
53357269 130600 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 423 5 1 5 4.6 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(-c3cccnc3)cc2C)CC1 nan
CHEMBL3681383 130600 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 423 5 1 5 4.6 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(-c3cccnc3)cc2C)CC1 nan
70686533 76618 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063381 76618 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmcl.2012.07.047
70686533 76618 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2063381 76618 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(F)cc12 10.1016/j.bmc.2012.09.028
71453344 81519 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 444 9 0 6 5.6 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160169 81519 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 444 9 0 6 5.6 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmc.2012.09.028
11983528 174905 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 418 4 1 6 3.5 COc1ccc(N2CCc3c(-n4ccc(N5CCCNC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL456448 174905 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 418 4 1 6 3.5 COc1ccc(N2CCc3c(-n4ccc(N5CCCNC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
44589351 177828 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 421 3 0 7 4.0 N#Cc1ccc(N2CCc3c(-n4ccc(-n5cccn5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
CHEMBL464390 177828 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 421 3 0 7 4.0 N#Cc1ccc(N2CCc3c(-n4ccc(-n5cccn5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
71451920 82607 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 461 9 0 9 4.2 CCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179185 82607 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 461 9 0 9 4.2 CCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
67380345 130598 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 425 4 1 3 5.0 O=C(N[C@H]1CC[C@H](Cn2cc3c(n2)CCC3)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3681381 130598 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 425 4 1 3 5.0 O=C(N[C@H]1CC[C@H](Cn2cc3c(n2)CCC3)CC1)c1cc(C(F)(F)F)ccc1Cl nan
21912127 97659 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 6 0 3 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1 10.1021/jm070578k
CHEMBL271117 97659 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 6 0 3 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1 10.1021/jm070578k
136042277 69985 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 339 5 1 4 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)[nH]c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939580 69985 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 339 5 1 4 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)[nH]c(=O)c12 10.1016/j.bmc.2011.11.015
11210737 139454 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 364 7 1 4 5.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794051 139454 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 364 7 1 4 5.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)n(C)c12 10.1021/acs.jmedchem.5b01715
54754517 65496 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 417 10 0 7 4.8 CCCN(CCC)c1cc(N(COC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830514 65496 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 417 10 0 7 4.8 CCCN(CCC)c1cc(N(COC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
10200135 77547 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 385 8 0 4 5.9 CCCN(CCC)c1c(CC)nn2c(-c3ccc(OC)cc3Cl)cccc12 10.1021/jm300259r
CHEMBL2087555 77547 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 385 8 0 4 5.9 CCCN(CCC)c1c(CC)nn2c(-c3ccc(OC)cc3Cl)cccc12 10.1021/jm300259r
22177744 64756 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 452 6 1 5 6.3 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC(F)(F)F)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819081 64756 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 452 6 1 5 6.3 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC(F)(F)F)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
46890982 6524 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 368 5 1 6 4.0 COc1cc(Cl)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2010.04.121
CHEMBL1082792 6524 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 368 5 1 6 4.0 COc1cc(Cl)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2010.04.121
46891494 6639 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 399 7 1 8 2.7 COC[C@H](C1CC1)n1nc(C)nc(Nc2ccc(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1083325 6639 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 399 7 1 8 2.7 COC[C@H](C1CC1)n1nc(C)nc(Nc2ccc(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
44191109 195529 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 363 6 1 6 3.9 COc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1OC 10.1021/jm900302q
CHEMBL554086 195529 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 363 6 1 6 3.9 COc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1OC 10.1021/jm900302q
21912175 155719 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 358 7 0 5 5.6 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1[N+](=O)[O-] 10.1021/jm070578k
CHEMBL405347 155719 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 358 7 0 5 5.6 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1[N+](=O)[O-] 10.1021/jm070578k
58012333 159481 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 405 6 1 4 6.8 CCC(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4101653 159481 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 405 6 1 4 6.8 CCC(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
21912175 155719 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 358 7 0 5 5.6 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1[N+](=O)[O-] 10.1021/jm070578k
CHEMBL405347 155719 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 358 7 0 5 5.6 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1[N+](=O)[O-] 10.1021/jm070578k
42618195 184286 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 413 9 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c(-c3cc(C)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL483993 184286 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 413 9 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c(-c3cc(C)c(OC)cc3C)c(C)nn12 10.1021/jm9000242
3495 1175 28 None - 1 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2007.06.077
5311055 1175 28 None - 1 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2007.06.077
CHEMBL9946 1175 28 None - 1 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2007.06.077
10277733 63142 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 484 6 0 4 7.6 CCCC(CCC)n1cc2c3c(nc(C)nc31)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL178949 63142 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 484 6 0 4 7.6 CCCC(CCC)n1cc2c3c(nc(C)nc31)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1016/j.bmcl.2007.06.077
45268771 196633 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 354 5 1 6 3.4 COc1ccc(Nc2nccn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
CHEMBL564291 196633 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 354 5 1 6 3.4 COc1ccc(Nc2nccn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
21912127 97659 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 6 0 3 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1 10.1021/jm070578k
CHEMBL271117 97659 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 6 0 3 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1 10.1021/jm070578k
137642541 158296 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 493 7 2 6 4.6 CCN(CC(=O)NC)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4089028 158296 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 493 7 2 6 4.6 CCN(CC(=O)NC)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
11164902 66302 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(C)C)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL184850 66302 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(C)C)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
70692630 75898 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Binding affinity to CRF1 receptor (unknown origin)Binding affinity to CRF1 receptor (unknown origin)
ChEMBL 376 7 1 4 6.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.ejmech.2021.114085
CHEMBL2049188 75898 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Binding affinity to CRF1 receptor (unknown origin)Binding affinity to CRF1 receptor (unknown origin)
ChEMBL 376 7 1 4 6.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.ejmech.2021.114085
70692630 75898 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 376 7 1 4 6.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.bmcl.2012.05.066
CHEMBL2049188 75898 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 376 7 1 4 6.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.bmcl.2012.05.066
71455053 81524 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 482 12 0 7 5.5 COCCN(CC(C)C)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160173 81524 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 482 12 0 7 5.5 COCCN(CC(C)C)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
70681900 75586 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 492 10 0 7 5.9 COCc1cc(OC)c(Oc2nc3cccc(N(CC4CC4)C4CCOCC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.05.066
CHEMBL2046529 75586 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 492 10 0 7 5.9 COCc1cc(OC)c(Oc2nc3cccc(N(CC4CC4)C4CCOCC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.05.066
44444337 94133 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 379 6 0 5 5.0 CCC(COC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)cc1C)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL249333 94133 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 379 6 0 5 5.0 CCC(COC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)cc1C)CC2 10.1016/j.bmcl.2007.06.077
44589317 177683 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 426 3 1 6 4.1 Cc1cc(-n2ccc(-n3cc[nH]c3=O)n2)c2c(n1)N(c1ccc(Cl)cc1Cl)CC2 10.1021/jm800744m
CHEMBL464184 177683 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 426 3 1 6 4.1 Cc1cc(-n2ccc(-n3cc[nH]c3=O)n2)c2c(n1)N(c1ccc(Cl)cc1Cl)CC2 10.1021/jm800744m
44589237 177011 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 454 4 0 8 4.9 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(OC(F)(F)F)c1 10.1021/jm800743q
CHEMBL462788 177011 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 454 4 0 8 4.9 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(OC(F)(F)F)c1 10.1021/jm800743q
56670270 65497 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 374 7 2 7 4.4 CCC(CC)Nc1c(C)c(Nc2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830515 65497 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 374 7 2 7 4.4 CCC(CC)Nc1c(C)c(Nc2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
21984613 77543 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 389 8 0 4 5.5 CCc1nn2c(-c3ccc(OC)cc3C)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087551 77543 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 389 8 0 4 5.5 CCc1nn2c(-c3ccc(OC)cc3C)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
15485774 196375 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 365 7 1 6 3.4 COCC(COC)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL562619 196375 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 365 7 1 6 3.4 COCC(COC)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
18392782 97968 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 325 5 0 3 6.1 C/C=C(\CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL272674 97968 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 325 5 0 3 6.1 C/C=C(\CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
44347046 114545 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 377 6 0 3 6.5 CCCCN(CC)c1cc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2004.05.056
CHEMBL333713 114545 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 377 6 0 3 6.5 CCCCN(CC)c1cc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2004.05.056
18392782 97968 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 325 5 0 3 6.1 C/C=C(\CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL272674 97968 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 325 5 0 3 6.1 C/C=C(\CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL5269179 193594 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition of human recombinant CRF1 in HEK cell line incubated for 2 hrs by MicroBeta scintillation counter methodInhibition of human recombinant CRF1 in HEK cell line incubated for 2 hrs by MicroBeta scintillation counter method
ChEMBL 381 4 0 4 6.6 CCC(CC)c1cc(C)nn2c(-c3sc4ccc(F)cc4c3C)c(C)nc12 10.1016/j.ejmech.2021.113867
16126888 69974 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 336 5 0 3 5.8 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939569 69974 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 336 5 0 3 5.8 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
24758071 69978 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 334 4 0 2 6.4 CCC(CC)c1cc(C)n2nc(-c3cc(C)c(C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939573 69978 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 334 4 0 2 6.4 CCC(CC)c1cc(C)n2nc(-c3cc(C)c(C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
58896526 176628 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 468 5 1 5 6.6 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(C(C)=O)c3ccc(Cl)cc3)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4592625 176628 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 468 5 1 5 6.6 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(C(C)=O)c3ccc(Cl)cc3)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4597886 176628 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 468 5 1 5 6.6 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(C(C)=O)c3ccc(Cl)cc3)c2n1C 10.1016/j.bmc.2016.08.005
53358603 130592 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 388 6 1 4 4.4 CCc1cc(CC)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
CHEMBL3681375 130592 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 388 6 1 4 4.4 CCc1cc(CC)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
11164902 66302 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL184850 66302 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
54580962 60655 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 366 6 0 5 4.2 CCCN(CCC)c1nc2c(c(-c3ccc(C)cc3C)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760259 60655 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 366 6 0 5 4.2 CCCN(CCC)c1nc2c(c(-c3ccc(C)cc3C)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
44392573 64290 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 475 10 0 6 5.8 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(OC)cc1Cc1cccnc1 10.1021/jm049787k
CHEMBL181007 64290 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 475 10 0 6 5.8 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(OC)cc1Cc1cccnc1 10.1021/jm049787k
44589206 176115 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 377 3 0 6 4.5 Cc1cc(F)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
CHEMBL459174 176115 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 377 3 0 6 4.5 Cc1cc(F)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
53358855 130595 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 413 4 1 3 5.2 Cc1cn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)nc1C nan
CHEMBL3681378 130595 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 413 4 1 3 5.2 Cc1cn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)nc1C nan
145958142 162058 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 383 6 1 6 4.8 CCCCN(CC)c1nc(C)nc2c1sc(=N)n2-c1c(C)cc(C)cc1C 10.1016/j.ejmech.2017.07.016
CHEMBL4160471 162058 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 383 6 1 6 4.8 CCCCN(CC)c1nc(C)nc2c1sc(=N)n2-c1c(C)cc(C)cc1C 10.1016/j.ejmech.2017.07.016
46881695 6923 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 350 6 1 7 3.0 COc1ccc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(OC)n1 10.1016/j.bmcl.2010.01.129
CHEMBL1084414 6923 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 350 6 1 7 3.0 COc1ccc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(OC)n1 10.1016/j.bmcl.2010.01.129
3520 3267 54 None 1 2 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmc.2016.11.011
9821250 3267 54 None 1 2 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmc.2016.11.011
CHEMBL309138 3267 54 None 1 2 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmc.2016.11.011
42618180 184357 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 5 1 7 3.7 COc1cc(C)c(-c2c(C)nn3c(NC4CCC4)nc(C)nc23)c(OC)c1 10.1021/jm9000242
CHEMBL484419 184357 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 5 1 7 3.7 COc1cc(C)c(-c2c(C)nn3c(NC4CCC4)nc(C)nc23)c(OC)c1 10.1021/jm9000242
42618232 184214 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 0 7 3.0 CCCN(C)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL483349 184214 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 0 7 3.0 CCCN(C)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
70909803 139453 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 468 8 1 5 7.2 CCCN(CCC)c1c(Cl)cc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794050 139453 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 468 8 1 5 7.2 CCCN(CCC)c1c(Cl)cc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
10110271 64739 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 379 6 2 6 4.6 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCN2 10.1016/j.bmc.2011.07.055
CHEMBL1819063 64739 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 379 6 2 6 4.6 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCN2 10.1016/j.bmc.2011.07.055
53358857 130597 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 425 4 1 3 5.0 O=C(N[C@H]1CC[C@H](Cn2ncc3c2CCC3)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3681380 130597 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 425 4 1 3 5.0 O=C(N[C@H]1CC[C@H](Cn2ncc3c2CCC3)CC1)c1cc(C(F)(F)F)ccc1Cl nan
24768346 85552 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 381 7 1 6 4.5 CCCCN(CC)c1nc(C)nc2c1NCCN2c1ccc(C(C)=O)cc1C 10.1021/jm0611410
CHEMBL227834 85552 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 381 7 1 6 4.5 CCCCN(CC)c1nc(C)nc2c1NCCN2c1ccc(C(C)=O)cc1C 10.1021/jm0611410
11188421 63889 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 388 7 0 4 5.4 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1 10.1021/jm049787k
CHEMBL180449 63889 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 388 7 0 4 5.4 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1 10.1021/jm049787k
44589236 178357 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 405 5 0 8 4.1 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(OC)c1 10.1021/jm800743q
CHEMBL465216 178357 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 405 5 0 8 4.1 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(OC)c1 10.1021/jm800743q
58223375 127867 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 11 0 9 4.6 COCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCC1 nan
CHEMBL3664580 127867 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 11 0 9 4.6 COCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCC1 nan
44190912 196369 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 382 4 1 5 4.8 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(Cl)cc2C#N)c1=O 10.1021/jm900302q
CHEMBL562550 196369 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 382 4 1 5 4.8 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(Cl)cc2C#N)c1=O 10.1021/jm900302q
44190824 196559 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 386 5 1 6 4.0 COC[C@@H](C)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL563819 196559 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 386 5 1 6 4.0 COC[C@@H](C)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900302q
10108936 98013 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 356 7 1 4 4.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C(N)=O)cc2C)c1C 10.1021/jm070578k
CHEMBL272910 98013 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 356 7 1 4 4.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C(N)=O)cc2C)c1C 10.1021/jm070578k
137640280 156741 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 518 7 1 5 6.8 CCN(CCC(F)(F)F)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4070523 156741 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 518 7 1 5 6.8 CCN(CCC(F)(F)F)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
145968300 164981 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 376 5 1 4 5.8 CCN(CC)c1cccc2nc(Nc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2018.01.020
CHEMBL4225516 164981 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 376 5 1 4 5.8 CCN(CC)c1cccc2nc(Nc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2018.01.020
10224109 124033 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 422 7 0 4 6.1 CCCCC(CC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL363023 124033 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 422 7 0 4 6.1 CCCCC(CC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
11489867 12392 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 446 9 1 6 4.4 COCCN(CCOC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
CHEMBL1185656 12392 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 446 9 1 6 4.4 COCCN(CCOC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
CHEMBL425542 12392 0 None - 0 Rat 7.8 pIC50 = 7.8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 446 9 1 6 4.4 COCCN(CCOC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
10108936 98013 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 356 7 1 4 4.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C(N)=O)cc2C)c1C 10.1021/jm070578k
CHEMBL272910 98013 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 356 7 1 4 4.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C(N)=O)cc2C)c1C 10.1021/jm070578k
24758074 69980 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 350 4 0 4 5.6 CCC(CC)c1cc(C)n2nc(-c3cc4c(cc3C)OCO4)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939575 69980 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 350 4 0 4 5.6 CCC(CC)c1cc(C)n2nc(-c3cc4c(cc3C)OCO4)c(C)cc12 10.1016/j.bmc.2011.11.015
177990 426 23 None -1 2 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.ejmech.2017.07.016
3489 426 23 None -1 2 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.ejmech.2017.07.016
CHEMBL296641 426 23 None -1 2 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.ejmech.2017.07.016
177990 426 23 None -1 2 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.ejmech.2014.03.040
3489 426 23 None -1 2 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.ejmech.2014.03.040
CHEMBL296641 426 23 None -1 2 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/j.ejmech.2014.03.040
44190560 196155 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 382 6 1 6 3.9 CCc1cn([C@H](C)C2CC2)c(=O)c(Nc2ccc(OC)nc2C(F)(F)F)n1 10.1021/jm900301y
CHEMBL561226 196155 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 382 6 1 6 3.9 CCc1cn([C@H](C)C2CC2)c(=O)c(Nc2ccc(OC)nc2C(F)(F)F)n1 10.1021/jm900301y
44190244 196720 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 337 5 1 4 4.7 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2ccc(Cl)cc2)c1=O 10.1021/jm900301y
CHEMBL564968 196720 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 337 5 1 4 4.7 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2ccc(Cl)cc2)c1=O 10.1021/jm900301y
21912198 97700 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 6 0 3 6.3 CCC(CC)Oc1c(C)c(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL271332 97700 0 None - 0 Rat 6.8 pIC50 = 6.8 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 6 0 3 6.3 CCC(CC)Oc1c(C)c(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
53357142 130599 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 440 5 1 4 5.3 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@@H](Cn2nc(-c3ccc(F)cc3)cc2C)CC1 nan
CHEMBL3681382 130599 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 440 5 1 4 5.3 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@@H](Cn2nc(-c3ccc(F)cc3)cc2C)CC1 nan
11773483 65573 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc([N+](=O)[O-])cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL183148 65573 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc([N+](=O)[O-])cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
11773483 65573 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc([N+](=O)[O-])cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL183148 65573 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc([N+](=O)[O-])cc3C)c(C)nn12 10.1021/jm040058e
155567202 175965 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 492 8 1 6 7.6 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3ccc(OC(C)C)cc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4588387 175965 0 None - 0 Human 5.8 pIC50 = 5.8 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 492 8 1 6 7.6 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3ccc(OC(C)C)cc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
21912198 97700 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 6 0 3 6.3 CCC(CC)Oc1c(C)c(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL271332 97700 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 6 0 3 6.3 CCC(CC)Oc1c(C)c(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
70682294 76617 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 394 8 0 5 5.2 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063380 76617 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 394 8 0 5 5.2 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmcl.2012.07.047
70682294 76617 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 394 8 0 5 5.2 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmc.2012.09.028
CHEMBL2063380 76617 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 394 8 0 5 5.2 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmc.2012.09.028
58223471 127869 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 463 12 0 9 4.3 COCCN(CC(C)C)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664582 127869 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 463 12 0 9 4.3 COCCN(CC(C)C)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
71580311 88436 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 431 9 1 8 3.3 COc1nc(Cl)nc(C)c1Nc1nc(Cl)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
CHEMBL2349562 88436 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 431 9 1 8 3.3 COc1nc(Cl)nc(C)c1Nc1nc(Cl)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
46890978 6733 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 312 4 1 5 3.6 Cc1cc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C)c1 10.1016/j.bmcl.2010.04.121
CHEMBL1083724 6733 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 312 4 1 5 3.6 Cc1cc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C)c1 10.1016/j.bmcl.2010.04.121
44190448 195133 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 439 4 0 6 4.2 COc1cc(Br)c2c(c1)OCCN2c1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900301y
CHEMBL550140 195133 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 439 4 0 6 4.2 COc1cc(Br)c2c(c1)OCCN2c1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900301y
44191111 196479 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 362 4 1 5 4.4 Cc1cc(Cl)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C#N 10.1021/jm900302q
CHEMBL563313 196479 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 362 4 1 5 4.4 Cc1cc(Cl)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C#N 10.1021/jm900302q
57397277 69991 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 381 6 0 5 5.3 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C(C)C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939586 69991 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 381 6 0 5 5.3 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C(C)C)c(=O)c12 10.1016/j.bmc.2011.11.015
42618175 184784 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 413 10 1 8 3.6 CCOCC(COCC)Nc1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL485140 184784 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 413 10 1 8 3.6 CCOCC(COCC)Nc1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
9885105 97999 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 357 8 0 4 6.1 CCOc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
CHEMBL272826 97999 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 357 8 0 4 6.1 CCOc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
11291949 127509 0 None - 1 Human 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3C)c(C)nn12 10.1021/jm040058e
CHEMBL366155 127509 0 None - 1 Human 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3C)c(C)nn12 10.1021/jm040058e
10216313 64355 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 410 7 0 6 4.5 CCCC(CCC)n1c(CC)nc2c1c(=O)n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1021/jm049787k
CHEMBL181258 64355 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 410 7 0 6 4.5 CCCC(CCC)n1c(CC)nc2c1c(=O)n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1021/jm049787k
60156090 77576 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 536 11 0 9 5.4 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4(C#N)CC4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087798 77576 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 536 11 0 9 5.4 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4(C#N)CC4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
11441103 175868 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 405 4 0 7 3.5 COc1ccc(N2CCc3c(-n4ccc(N5CCOC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL458600 175868 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 405 4 0 7 3.5 COc1ccc(N2CCc3c(-n4ccc(N5CCOC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
70682070 75899 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 390 8 2 4 7.0 CCCC(CCC)Nc1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.bmcl.2012.05.066
CHEMBL2049189 75899 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 390 8 2 4 7.0 CCCC(CCC)Nc1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.bmcl.2012.05.066
11260682 11755 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 392 5 2 4 5.4 CCC(CC)Nc1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl 10.1021/jm049737f
CHEMBL1181621 11755 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 392 5 2 4 5.4 CCC(CC)Nc1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl 10.1021/jm049737f
CHEMBL185736 11755 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 392 5 2 4 5.4 CCC(CC)Nc1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl 10.1021/jm049737f
CHEMBL526149 215675 10 None - 0 Human 8.7 pIC50 = 8.7 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL None None None CSCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(=O)O)[C@@H](C)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(N)=O 10.1021/jm9000242
57390212 70007 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 367 5 0 5 4.5 CCC(CC)c1cc(C)n2nc(-c3c(C)cc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939601 70007 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 367 5 0 5 4.5 CCC(CC)c1cc(C)n2nc(-c3c(C)cc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL526149 215675 10 None - 0 Human 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cellsDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cells
ChEMBL None None None CSCC[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(=O)O)[C@@H](C)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(N)=O 10.1021/jm900025h
9949999 97583 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 0 4 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(OC)cc2C)c1C 10.1021/jm070578k
CHEMBL270764 97583 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 0 4 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(OC)cc2C)c1C 10.1021/jm070578k
9949999 97583 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 0 4 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(OC)cc2C)c1C 10.1021/jm070578k
CHEMBL270764 97583 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 0 4 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(OC)cc2C)c1C 10.1021/jm070578k
46891090 6821 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 418 7 1 6 5.0 CCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1083947 6821 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 418 7 1 6 5.0 CCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
46881794 7337 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 384 6 1 6 4.2 Cc1cc(OC(F)F)nc(C)c1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1086181 7337 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 384 6 1 6 4.2 Cc1cc(OC(F)F)nc(C)c1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1016/j.bmcl.2010.01.129
44190146 197835 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 381 8 1 7 3.1 COCC(COC)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL572347 197835 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 381 8 1 7 3.1 COCC(COC)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
42618179 184534 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 383 7 1 7 4.3 CCCC(C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL484781 184534 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 383 7 1 7 4.3 CCCC(C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
42618171 179997 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 378 7 0 7 3.9 CCCN(CCC#N)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL474700 179997 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 378 7 0 7 3.9 CCCN(CCC#N)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
24768332 85583 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 385 8 1 7 4.0 CCCCN(CC)c1cc(C)nc2c1NCCN2c1ccc(OC)nc1OC 10.1021/jm0611410
CHEMBL228168 85583 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 385 8 1 7 4.0 CCCCN(CC)c1cc(C)nc2c1NCCN2c1ccc(OC)nc1OC 10.1021/jm0611410
11176967 67242 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 397 6 1 5 4.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1Cl 10.1021/jm049737f
CHEMBL187987 67242 0 None - 0 Rat 8.7 pIC50 = 8.7 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 397 6 1 5 4.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1Cl 10.1021/jm049737f
46891437 6412 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 399 7 1 8 2.7 COC[C@@H](C1CC1)n1nc(C)nc(Nc2ccc(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1082358 6412 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 399 7 1 8 2.7 COC[C@@H](C1CC1)n1nc(C)nc(Nc2ccc(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
42618169 180837 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 7 0 6 4.4 CCCCN(CC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL475705 180837 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 7 0 6 4.4 CCCCN(CC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
44190916 196746 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 443 6 1 5 5.6 CC[C@H](COC)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL565182 196746 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 443 6 1 5 5.6 CC[C@H](COC)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
11588927 65507 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 377 7 1 6 5.4 CCc1cc(OC)ccc1Nc1nc2ccnn2c2c1ccn2C(CC)CC 10.1016/j.bmc.2011.08.055
CHEMBL1830524 65507 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 377 7 1 6 5.4 CCc1cc(OC)ccc1Nc1nc2ccnn2c2c1ccn2C(CC)CC 10.1016/j.bmc.2011.08.055
71456930 81990 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 409 9 1 6 4.2 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OCCF)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL2165196 81990 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 409 9 1 6 4.2 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OCCF)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
46891438 6413 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 413 8 1 8 3.1 CCOc1ccc(Nc2nc(C)nn([C@@H](COC)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1082359 6413 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 413 8 1 8 3.1 CCOc1ccc(Nc2nc(C)nn([C@@H](COC)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
44190336 194931 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 345 5 1 4 4.9 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL541756 194931 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 345 5 1 4 4.9 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(C)cc2C)c1=O 10.1021/jm900301y
44189949 195961 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 7 1 4 5.7 CCCC(CCC)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL559633 195961 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 361 7 1 4 5.7 CCCC(CCC)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
44190239 196637 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 382 4 1 5 4.8 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900301y
CHEMBL564303 196637 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 382 4 1 5 4.8 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900301y
42618235 184192 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 382 8 0 7 4.1 CCCCN(CCC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL483162 184192 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 382 8 0 7 4.1 CCCCN(CCC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
44190239 196637 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 382 4 1 5 4.8 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL564303 196637 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 382 4 1 5 4.8 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900302q
42618191 184359 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 394 7 0 8 3.5 CCN(CCC#N)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL484421 184359 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 394 7 0 8 3.5 CCN(CCC#N)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
42618168 180656 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 7 0 6 4.4 CCCN(CCC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL475506 180656 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 7 0 6 4.4 CCCN(CCC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
57393711 69975 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 353 5 0 5 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939570 69975 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 353 5 0 5 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
9952426 97703 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 391 6 0 3 6.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(Br)cc2C)c1C 10.1021/jm070578k
CHEMBL271344 97703 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 391 6 0 3 6.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(Br)cc2C)c1C 10.1021/jm070578k
11249766 11759 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 430 8 1 5 5.1 CCCN(CCOC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
CHEMBL1181636 11759 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 430 8 1 5 5.1 CCCN(CCOC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
CHEMBL186517 11759 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 430 8 1 5 5.1 CCCN(CCOC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049737f
9952426 97703 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 391 6 0 3 6.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(Br)cc2C)c1C 10.1021/jm070578k
CHEMBL271344 97703 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 391 6 0 3 6.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(Br)cc2C)c1C 10.1021/jm070578k
46891287 6881 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 397 6 1 7 3.8 CCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1084203 6881 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 397 6 1 7 3.8 CCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
46881747 5596 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 362 6 1 6 4.0 CCOc1nc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.01.129
CHEMBL1077249 5596 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 362 6 1 6 4.0 CCOc1nc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.01.129
42618193 184158 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 413 9 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL482976 184158 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 413 9 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3C)c(C)nn12 10.1021/jm9000242
44190149 195060 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 396 5 1 5 5.2 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900301y
CHEMBL549538 195060 0 None - 0 Rat 8.6 pIC50 = 8.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 396 5 1 5 5.2 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900301y
136164073 8156 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 411 7 2 7 3.5 COCC(COC)NC1NC(C)=Nc2c(-c3ccc(Cl)cc3Cl)c(C)nn21 10.1016/j.bmcl.2010.01.129
CHEMBL1091818 8156 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 411 7 2 7 3.5 COCC(COC)NC1NC(C)=Nc2c(-c3ccc(Cl)cc3Cl)c(C)nn21 10.1016/j.bmcl.2010.01.129
15485770 197594 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 333 5 1 4 4.9 CCC(CC)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL570546 197594 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 333 5 1 4 4.9 CCC(CC)n1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
42618178 191689 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 369 6 1 7 3.9 CC[C@H](C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL519677 191689 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 369 6 1 7 3.9 CC[C@H](C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
44190827 196157 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 362 4 1 5 4.4 Cc1cc(C#N)cc(Cl)c1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900302q
CHEMBL561230 196157 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 362 4 1 5 4.4 Cc1cc(C#N)cc(Cl)c1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900302q
58223380 127868 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 11 0 9 5.0 COCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCCC1 nan
CHEMBL3664581 127868 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 11 0 9 5.0 COCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCCC1 nan
56663336 65310 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 387 8 0 6 4.8 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828896 65310 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 387 8 0 6 4.8 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56683765 65505 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 388 8 0 7 4.2 CCCN(CCC)c1nc(N(C)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830522 65505 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 388 8 0 7 4.2 CCCN(CCC)c1nc(N(C)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
21984697 77550 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 409 9 0 4 5.8 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CCCF)CC1CC1 10.1021/jm300259r
CHEMBL2087558 77550 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 409 9 0 4 5.8 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CCCF)CC1CC1 10.1021/jm300259r
46891336 6407 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 359 7 1 8 2.3 COCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1082340 6407 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 359 7 1 8 2.3 COCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
46891092 7232 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 416 5 1 7 3.4 Cc1nc(Nc2c(Cl)cc(S(C)(=O)=O)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1085734 7232 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 416 5 1 7 3.4 Cc1nc(Nc2c(Cl)cc(S(C)(=O)=O)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
9885105 97999 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 357 8 0 4 6.1 CCOc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
CHEMBL272826 97999 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 357 8 0 4 6.1 CCOc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
57786312 164966 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 423 4 0 4 6.6 CCC(OC)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4225316 164966 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 423 4 0 4 6.6 CCC(OC)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
21084107 77558 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 479 10 1 7 4.7 CCc1nn2c(-c3c(OC)cc(CO)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087566 77558 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 479 10 1 7 4.7 CCc1nn2c(-c3c(OC)cc(CO)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
11177197 167641 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 404 7 1 4 6.6 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2018.01.020
CHEMBL4226111 167641 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 404 7 1 4 6.6 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2018.01.020
CHEMBL4301639 167641 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 404 7 1 4 6.6 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2018.01.020
71458704 81517 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 410 9 0 6 4.9 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmc.2012.09.028
CHEMBL2160167 81517 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 410 9 0 6 4.9 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)ccc12 10.1016/j.bmc.2012.09.028
44589304 176020 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 388 3 0 7 4.1 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(F)c1 10.1021/jm800743q
CHEMBL458981 176020 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 388 3 0 7 4.1 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(F)c1 10.1021/jm800743q
53328045 130606 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 441 6 1 3 5.7 CCc1cc(CC)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
CHEMBL3681389 130606 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 441 6 1 3 5.7 CCc1cc(CC)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)n1 nan
71449777 81993 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 453 10 1 7 4.1 COCC(COC)n1cc(Cl)nc(Nc2c(Cl)cc(OCCF)cc2Cl)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL2165199 81993 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 453 10 1 7 4.1 COCC(COC)n1cc(Cl)nc(Nc2c(Cl)cc(OCCF)cc2Cl)c1=O 10.1016/j.bmcl.2012.08.112
24768338 85540 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 415 9 1 8 3.5 CCCN(CCOC)c1nc(C)nc2c1NCCN2c1cc(OC)c(OC)cc1C 10.1021/jm0611410
CHEMBL227724 85540 0 None - 0 Rat 6.7 pIC50 = 6.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 415 9 1 8 3.5 CCCN(CCOC)c1nc(C)nc2c1NCCN2c1cc(OC)c(OC)cc1C 10.1021/jm0611410
57786300 164948 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 407 3 0 4 6.1 CCC(=O)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4224989 164948 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 407 3 0 4 6.1 CCC(=O)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
57785808 164949 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 489 5 0 6 6.0 CCc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4225039 164949 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 489 5 0 6 6.0 CCc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
70690703 76610 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 380 6 0 5 4.7 COCc1cc(OC)c(-c2nc3c(C)ccc(N(C)C)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
CHEMBL2063371 76610 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 380 6 0 5 4.7 COCc1cc(OC)c(-c2nc3c(C)ccc(N(C)C)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
56683689 65315 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 427 10 0 6 5.6 CCCN(CCC)c1cc(N(CC2CC2)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828901 65315 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 427 10 0 6 5.6 CCCN(CCC)c1cc(N(CC2CC2)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
44589306 174988 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 406 5 0 9 3.5 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(OC)n1 10.1021/jm800743q
CHEMBL456651 174988 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 406 5 0 9 3.5 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(OC)n1 10.1021/jm800743q
53358856 130596 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 413 4 1 3 5.2 Cc1cnn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1C nan
CHEMBL3681379 130596 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 413 4 1 3 5.2 Cc1cnn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c1C nan
58896446 139505 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 412 8 1 4 7.0 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Cl)cc3C(C)C)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3792636 139505 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 412 8 1 4 7.0 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Cl)cc3C(C)C)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794595 139505 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 412 8 1 4 7.0 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(Cl)cc3C(C)C)n(C)c12 10.1021/acs.jmedchem.5b01715
60155708 77553 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 447 8 0 5 5.8 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087561 77553 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 447 8 0 5 5.8 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
60155709 77554 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 463 9 0 6 5.5 CCc1nn2c(-c3c(OC)cc(C)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087562 77554 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 463 9 0 6 5.5 CCc1nn2c(-c3c(OC)cc(C)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
10135150 64751 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 392 6 1 5 5.4 CCC(CC)Nc1c2c(nc3c(-c4cc(C)c(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819075 64751 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 392 6 1 5 5.4 CCC(CC)Nc1c2c(nc3c(-c4cc(C)c(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
22177742 64762 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 400 6 1 6 5.0 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)COC2 10.1016/j.bmc.2011.07.055
CHEMBL1819087 64762 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 400 6 1 6 5.0 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)COC2 10.1016/j.bmc.2011.07.055
24964084 156544 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 419 6 1 4 6.0 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(C(N)=O)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4068170 156544 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 419 6 1 4 6.0 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(C(N)=O)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
11948286 156669 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 410 5 0 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4069551 156669 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 410 5 0 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
53357920 130611 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 427 5 1 3 5.4 CCc1cc(C)nn1C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3681394 130611 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 427 5 1 3 5.4 CCc1cc(C)nn1C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
10294192 65206 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 396 7 0 4 5.7 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1c(C)cc(C)cc1C 10.1021/jm049787k
CHEMBL182550 65206 0 None - 0 Rat 7.7 pIC50 = 7.7 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 396 7 0 4 5.7 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1c(C)cc(C)cc1C 10.1021/jm049787k
58896429 173325 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 510 7 1 6 7.1 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(CC3CCOC3)c3ccc(Cl)cc3)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4526475 173325 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 510 7 1 6 7.1 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(CC3CCOC3)c3ccc(Cl)cc3)c2n1C 10.1016/j.bmc.2016.08.005
58896417 139501 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 426 8 1 4 7.3 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)n(-c3ccccc3)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793751 139501 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 426 8 1 4 7.3 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)n(-c3ccccc3)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794591 139501 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 426 8 1 4 7.3 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)n(-c3ccccc3)c12 10.1021/acs.jmedchem.5b01715
58223481 82599 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 517 11 1 10 4.0 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4(O)CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179177 82599 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 517 11 1 10 4.0 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4(O)CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
44589331 175480 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 378 3 0 6 4.2 Cc1cc(C#N)ccc1N1CCc2c(-n3ccc(-c4ccccn4)n3)ccnc21 10.1021/jm800743q
CHEMBL457741 175480 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 378 3 0 6 4.2 Cc1cc(C#N)ccc1N1CCc2c(-n3ccc(-c4ccccn4)n3)ccnc21 10.1021/jm800743q
71453343 81511 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160160 81511 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 412 8 0 5 5.4 CCN(CC)c1ccc(F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
44589239 190490 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 404 3 0 7 4.6 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
CHEMBL517910 190490 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 404 3 0 7 4.6 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
46891491 6946 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 383 6 1 7 3.5 CCOc1ccc(Nc2nc(C)nn([C@@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1084500 6946 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 383 6 1 7 3.5 CCOc1ccc(Nc2nc(C)nn([C@@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
46891390 7122 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 434 8 1 7 4.2 COC[C@@H](C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1085244 7122 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 434 8 1 7 4.2 COC[C@@H](C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
42618217 184623 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 400 9 0 9 2.2 COCCN(CCOC)c1nc(C)nc2c(-c3cnc(OC)cc3C)c(C)nn12 10.1021/jm900025h
CHEMBL484930 184623 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 400 9 0 9 2.2 COCCN(CCOC)c1nc(C)nc2c(-c3cnc(OC)cc3C)c(C)nn12 10.1021/jm900025h
44589256 189642 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 457 4 0 8 4.1 CS(=O)(=O)c1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
CHEMBL515070 189642 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 457 4 0 8 4.1 CS(=O)(=O)c1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
58223424 127871 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 431 9 0 8 4.6 CCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCC1 nan
CHEMBL3664584 127871 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 431 9 0 8 4.6 CCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCC1 nan
127030314 139389 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 406 6 1 5 5.8 CCN(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793277 139389 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 406 6 1 5 5.8 CCN(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
21984771 77545 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 403 8 0 4 5.8 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
CHEMBL2087553 77545 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 403 8 0 4 5.8 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CC1)CC1CC1 10.1021/jm300259r
127030314 139389 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 406 6 1 5 5.8 CCN(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL3793277 139389 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 406 6 1 5 5.8 CCN(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
42618176 184354 1 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 337 4 1 6 3.7 COc1ccc(-c2c(C)nn3c(NC4CCC4)nc(C)nc23)c(C)c1 10.1021/jm9000242
CHEMBL484407 184354 1 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 337 4 1 6 3.7 COc1ccc(-c2c(C)nn3c(NC4CCC4)nc(C)nc23)c(C)c1 10.1021/jm9000242
42618216 192119 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 6 1 7 3.8 CCC(CC)Nc1nc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm900025h
CHEMBL520344 192119 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 6 1 7 3.8 CCC(CC)Nc1nc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm900025h
22177988 64742 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 364 6 1 5 4.8 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)cnn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819066 64742 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 364 6 1 5 4.8 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)cnn13)CCC2 10.1016/j.bmc.2011.07.055
46881863 5602 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 365 6 1 8 2.7 COc1nc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(OC)n1 10.1016/j.bmcl.2010.01.129
CHEMBL1077299 5602 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 365 6 1 8 2.7 COc1nc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(OC)n1 10.1016/j.bmcl.2010.01.129
90654669 110074 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 398 9 1 5 6.2 CCCN(CC1CC1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)c1SCC 10.1016/j.ejmech.2014.03.040
CHEMBL3235706 110074 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 398 9 1 5 6.2 CCCN(CC1CC1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)c1SCC 10.1016/j.ejmech.2014.03.040
70688637 76616 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 490 9 0 6 6.1 COCc1cc(OC)c(-c2nc3c(C)ccc(N(CC4CC4)C4CCOCC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
CHEMBL2063377 76616 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 490 9 0 6 6.1 COCc1cc(OC)c(-c2nc3c(C)ccc(N(CC4CC4)C4CCOCC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
58223432 127856 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 477 14 0 9 4.9 CCCCN(CCOC)c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12 nan
CHEMBL3664569 127856 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 477 14 0 9 4.9 CCCCN(CCOC)c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12 nan
58223378 127863 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 12 0 9 4.5 COCCN(CC1CCC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664576 127863 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 12 0 9 4.5 COCCN(CC1CCC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
60155887 77573 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 465 9 0 7 5.0 COc1cc(C)cc(OC)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(OC)nn12 10.1021/jm300259r
CHEMBL2087795 77573 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 465 9 0 7 5.0 COc1cc(C)cc(OC)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(OC)nn12 10.1021/jm300259r
21912058 97699 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 356 7 0 4 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1N(C)C 10.1021/jm070578k
CHEMBL271329 97699 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 356 7 0 4 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1N(C)C 10.1021/jm070578k
155552287 174072 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 465 7 1 7 6.2 COc1ccc(N(c2cccc3nc(Nc4c(C)cc(Cl)cc4OC)n(C)c23)C(C)C)cn1 10.1016/j.bmc.2016.08.005
CHEMBL4544244 174072 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 465 7 1 7 6.2 COc1ccc(N(c2cccc3nc(Nc4c(C)cc(Cl)cc4OC)n(C)c23)C(C)C)cn1 10.1016/j.bmc.2016.08.005
58896465 176096 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 468 6 1 5 7.5 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3ccc(Cl)cc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4591335 176096 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 468 6 1 5 7.5 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3ccc(Cl)cc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
10204603 63345 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 456 4 0 4 6.8 CCC(CC)n1cc2c3c(nc(C)nc31)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL179435 63345 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 456 4 0 4 6.8 CCC(CC)n1cc2c3c(nc(C)nc31)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1016/j.bmcl.2007.06.077
21912058 97699 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 356 7 0 4 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1N(C)C 10.1021/jm070578k
CHEMBL271329 97699 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 356 7 0 4 5.7 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1N(C)C 10.1021/jm070578k
42618207 179806 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 381 6 1 7 4.1 CCC(CC)Nc1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL474491 179806 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 381 6 1 7 4.1 CCC(CC)Nc1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
58896492 139500 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 2 3 5.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)[nH]c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793362 139500 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 2 3 5.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)[nH]c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794590 139500 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 2 3 5.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)[nH]c12 10.1021/acs.jmedchem.5b01715
71457263 82616 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 445 9 0 8 4.6 CCCN(c1c(OC)nn2c(-c3ccc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179194 82616 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 445 9 0 8 4.6 CCCN(c1c(OC)nn2c(-c3ccc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
58317279 126537 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 394 4 1 4 4.5 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(C)c(Cl)c2C)CC1 nan
CHEMBL3652115 126537 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 394 4 1 4 4.5 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(C)c(Cl)c2C)CC1 nan
44589329 175642 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 403 4 0 8 3.9 Cc1nc(N(C)C)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
CHEMBL458101 175642 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 403 4 0 8 3.9 Cc1nc(N(C)C)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
44589223 189525 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 443 4 0 7 5.3 Cc1cc(OC(F)(F)F)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
CHEMBL514126 189525 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 443 4 0 7 5.3 Cc1cc(OC(F)(F)F)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
58223390 127844 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 433 11 0 8 4.9 CCCN(CCC)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664557 127844 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 433 11 0 8 4.9 CCCN(CCC)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
58223381 127861 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 11 0 9 4.6 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12)C1CCOC1 nan
CHEMBL3664574 127861 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 11 0 9 4.6 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12)C1CCOC1 nan
58223490 127878 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 445 9 0 8 5.0 CCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCC1 nan
CHEMBL3664590 127878 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 445 9 0 8 5.0 CCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCC1 nan
46891288 6882 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 329 5 1 7 2.7 COc1nc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.04.121
CHEMBL1084204 6882 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 329 5 1 7 2.7 COc1nc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.04.121
11304337 64847 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 406 4 0 4 5.3 CCc1nc2c(n1C(C)C1CCC1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL182068 64847 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 406 4 0 4 5.3 CCc1nc2c(n1C(C)C1CCC1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
46891229 6548 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 407 4 1 6 4.4 Cc1nc(Nc2c(Cl)cc(C(F)(F)F)nc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1082956 6548 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 407 4 1 6 4.4 Cc1nc(Nc2c(Cl)cc(C(F)(F)F)nc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
53357410 126538 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 360 4 1 4 3.8 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
CHEMBL3652116 126538 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 360 4 1 4 3.8 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
60155989 77577 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 513 11 0 9 4.5 COCc1cc(OC)c(-c2cccc3c(N(CC4CC4)CC4COCCO4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087799 77577 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 513 11 0 9 4.5 COCc1cc(OC)c(-c2cccc3c(N(CC4CC4)CC4COCCO4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
46891552 7342 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 413 8 1 8 3.1 CCOc1ccc(Nc2nc(C)nn([C@H](COC)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1086239 7342 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 413 8 1 8 3.1 CCOc1ccc(Nc2nc(C)nn([C@H](COC)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
58896411 176205 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 464 7 1 6 6.8 COc1ccc(N(c2cccc3nc(Nc4c(C)cc(Cl)cc4OC)n(C)c23)C(C)C)cc1 10.1016/j.bmc.2016.08.005
CHEMBL4593848 176205 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 464 7 1 6 6.8 COc1ccc(N(c2cccc3nc(Nc4c(C)cc(Cl)cc4OC)n(C)c23)C(C)C)cc1 10.1016/j.bmc.2016.08.005
10136833 122343 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 418 8 0 5 5.4 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(OC)cc1Cl 10.1021/jm049787k
CHEMBL359923 122343 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 418 8 0 5 5.4 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(OC)cc1Cl 10.1021/jm049787k
44589092 176015 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 481 3 0 6 6.1 FC(F)(F)c1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
CHEMBL458968 176015 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 481 3 0 6 6.1 FC(F)(F)c1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
46891187 6643 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 363 4 1 6 3.8 Cc1nc(Nc2cc(Cl)c(C#N)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1083342 6643 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 363 4 1 6 3.8 Cc1nc(Nc2cc(Cl)c(C#N)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
137635894 155911 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 507 7 1 6 5.0 CCN(CC(=O)N(C)C)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4060825 155911 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 507 7 1 6 5.0 CCN(CC(=O)N(C)C)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
57786068 165047 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 389 4 0 4 5.3 CCN(CC)c1cccc2nc3n(c12)CCOC3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4226353 165047 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 389 4 0 4 5.3 CCN(CC)c1cccc2nc3n(c12)CCOC3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
90654666 110071 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 404 10 1 7 4.3 COCCN(CCOC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)c1SC 10.1016/j.ejmech.2014.03.040
CHEMBL3235700 110071 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 404 10 1 7 4.3 COCCN(CCOC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)c1SC 10.1016/j.ejmech.2014.03.040
25149257 189543 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 397 3 0 8 4.2 Cc1cc(-n2ccc(-c3nccs3)n2)c2cnn(-c3ccc(C#N)cc3C)c2n1 10.1021/jm800743q
CHEMBL514272 189543 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 397 3 0 8 4.2 Cc1cc(-n2ccc(-c3nccs3)n2)c2cnn(-c3ccc(C#N)cc3C)c2n1 10.1021/jm800743q
70692845 76607 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 422 10 0 5 6.0 CCCN(CCC)c1cccc2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063368 76607 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 422 10 0 5 6.0 CCCN(CCC)c1cccc2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
46891156 7237 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 342 6 1 6 3.7 CCOc1cc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.04.121
CHEMBL1085754 7237 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 342 6 1 6 3.7 CCOc1cc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.04.121
21912152 95962 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 5 0 3 5.6 CCC(C)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL259467 95962 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 5 0 3 5.6 CCC(C)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
3520 3267 54 None 1 2 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm800744m
9821250 3267 54 None 1 2 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm800744m
CHEMBL309138 3267 54 None 1 2 Human 7.6 pIC50 = 7.6 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm800744m
21912152 95962 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 5 0 3 5.6 CCC(C)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL259467 95962 0 None - 0 Rat 7.6 pIC50 = 7.6 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 313 5 0 3 5.6 CCC(C)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
44190339 196120 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 363 6 2 6 3.6 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(O)cc2C)c1=O 10.1021/jm900301y
CHEMBL561024 196120 0 None - 0 Rat 6.6 pIC50 = 6.6 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 363 6 2 6 3.6 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(O)cc2C)c1=O 10.1021/jm900301y
70692847 76615 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 504 10 0 6 6.3 COCc1cc(OC)c(-c2nc3c(C)ccc(N(CC4CCOCC4)CC4CC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
CHEMBL2063376 76615 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 504 10 0 6 6.3 COCc1cc(OC)c(-c2nc3c(C)ccc(N(CC4CCOCC4)CC4CC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
71458702 81514 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 462 8 0 5 6.2 CCN(CC)c1ccc(C(F)(F)F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160163 81514 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 462 8 0 5 6.2 CCN(CC)c1ccc(C(F)(F)F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
11774042 203352 0 None - 1 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm040058e
CHEMBL65078 203352 0 None - 1 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm040058e
58223393 127832 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 465 10 1 8 4.6 CCCN(CCC)c1c(C)nn2c(-c3c(O)cc(COC)cc3OC)c([S+](C)[O-])sc12 nan
CHEMBL3664545 127832 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 465 10 1 8 4.6 CCCN(CCC)c1c(C)nn2c(-c3c(O)cc(COC)cc3OC)c([S+](C)[O-])sc12 nan
10309819 65216 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 408 5 0 6 4.1 CCc1nc2c(c(=O)n(C)c(=O)n2-c2ccc(Cl)cc2Cl)n1C(CC)CC 10.1021/jm049787k
CHEMBL182591 65216 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 408 5 0 6 4.1 CCc1nc2c(c(=O)n(C)c(=O)n2-c2ccc(Cl)cc2Cl)n1C(CC)CC 10.1021/jm049787k
56668632 64758 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 434 7 1 5 6.0 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC(F)F)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819083 64758 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 434 7 1 5 6.0 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC(F)F)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
46891286 6623 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 413 8 1 8 3.1 CCOc1ccc(Nc2nc(C)nn(C(COC)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1083293 6623 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 413 8 1 8 3.1 CCOc1ccc(Nc2nc(C)nn(C(COC)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
42618219 184134 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 1 7 3.7 CCC(CC)Nc1nc(C)nc2c(-c3cnc(OC)cc3C)c(C)nn12 10.1021/jm900025h
CHEMBL482752 184134 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 1 7 3.7 CCC(CC)Nc1nc(C)nc2c(-c3cnc(OC)cc3C)c(C)nn12 10.1021/jm900025h
42618229 189797 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 396 8 0 8 3.0 COCCN(CC1CC1)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL516242 189797 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 396 8 0 8 3.0 COCCN(CC1CC1)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
42618220 191884 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 1 7 3.7 CCC(CC)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL519967 191884 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 1 7 3.7 CCC(CC)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
44190730 195973 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 331 4 1 4 4.5 Cc1cn([C@H](C)C2CC2)c(=O)c(Nc2c(C)cc(Cl)cc2C)n1 10.1021/jm900302q
CHEMBL559701 195973 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 331 4 1 4 4.5 Cc1cn([C@H](C)C2CC2)c(=O)c(Nc2c(C)cc(Cl)cc2C)n1 10.1021/jm900302q
21912269 168910 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 357 8 0 4 5.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(COC)cc2C)c1C 10.1021/jm070578k
CHEMBL438553 168910 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 357 8 0 4 5.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(COC)cc2C)c1C 10.1021/jm070578k
11153312 65506 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 383 6 1 6 5.5 CCC(CC)n1ccc2c(Nc3ccc(OC)cc3Cl)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
CHEMBL1830523 65506 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 383 6 1 6 5.5 CCC(CC)n1ccc2c(Nc3ccc(OC)cc3Cl)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
71580316 88441 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 441 8 0 6 4.2 COc1cc(Cl)c2c(c1)CCN2c1nc(Cl)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
CHEMBL2349567 88441 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 441 8 0 6 4.2 COc1cc(Cl)c2c(c1)CCN2c1nc(Cl)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
21912269 168910 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 357 8 0 4 5.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(COC)cc2C)c1C 10.1021/jm070578k
CHEMBL438553 168910 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 357 8 0 4 5.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(COC)cc2C)c1C 10.1021/jm070578k
42618192 192593 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 409 5 0 7 4.5 CCC1CCCCN1c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL521457 192593 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 409 5 0 7 4.5 CCC1CCCCN1c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
57398971 69995 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 393 7 0 5 5.1 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939590 69995 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 393 7 0 5 5.1 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
24768339 85566 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 377 6 1 5 4.3 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1C 10.1021/jm0611410
CHEMBL227946 85566 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 377 6 1 5 4.3 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1C 10.1021/jm0611410
11421422 11765 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 431 6 1 5 5.3 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1c(Cl)cc(C#N)cc1Cl 10.1021/jm049737f
CHEMBL1181649 11765 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 431 6 1 5 5.3 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1c(Cl)cc(C#N)cc1Cl 10.1021/jm049737f
CHEMBL187410 11765 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 431 6 1 5 5.3 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1c(Cl)cc(C#N)cc1Cl 10.1021/jm049737f
9820671 188818 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 369 6 1 7 3.9 CC[C@@H](C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL506214 188818 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 369 6 1 7 3.9 CC[C@@H](C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
24768340 142925 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 363 6 1 5 4.8 CCCCN(CC)c1cc(C)nc2c1NCCN2c1ccc(C#N)cc1C 10.1021/jm0611410
CHEMBL389387 142925 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 363 6 1 5 4.8 CCCCN(CC)c1cc(C)nc2c1NCCN2c1ccc(C#N)cc1C 10.1021/jm0611410
46891387 6484 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 369 5 1 7 3.1 COc1ccc(Nc2nc(C)nn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1082669 6484 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 369 5 1 7 3.1 COc1ccc(Nc2nc(C)nn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
42618223 179275 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 1 7 3.7 CCCC(C)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL473069 179275 0 None - 0 Rat 8.5 pIC50 = 8.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 1 7 3.7 CCCC(C)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
46891285 6622 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 397 7 1 7 3.9 CCOc1ccc(Nc2nc(C)nn(C(CC)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1083292 6622 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 397 7 1 7 3.9 CCOc1ccc(Nc2nc(C)nn(C(CC)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
46891231 6696 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 383 6 1 7 3.5 CCC(C1CC1)n1nc(C)nc(Nc2ccc(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1083590 6696 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 383 6 1 7 3.5 CCC(C1CC1)n1nc(C)nc(Nc2ccc(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
46891232 6697 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 399 7 1 8 2.7 COCC(C1CC1)n1nc(C)nc(Nc2ccc(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1083591 6697 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 399 7 1 8 2.7 COCC(C1CC1)n1nc(C)nc(Nc2ccc(OC)nc2C(F)(F)F)c1=O 10.1016/j.bmcl.2010.04.121
9858549 97670 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 5.9 CCC(CC)Oc1cc(C)nc(Nc2c(C)cc(C)cc2C)c1C 10.1021/jm070579c
CHEMBL271197 97670 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 5.9 CCC(CC)Oc1cc(C)nc(Nc2c(C)cc(C)cc2C)c1C 10.1021/jm070579c
44191009 196218 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 455 7 1 4 7.1 CCCC(CCC)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL561553 196218 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 455 7 1 4 7.1 CCCC(CCC)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
9858549 97670 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 5.9 CCC(CC)Oc1cc(C)nc(Nc2c(C)cc(C)cc2C)c1C 10.1021/jm070579c
CHEMBL271197 97670 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 5.9 CCC(CC)Oc1cc(C)nc(Nc2c(C)cc(C)cc2C)c1C 10.1021/jm070579c
42618182 191901 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 397 8 0 7 4.4 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL519999 191901 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 397 8 0 7 4.4 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
57397276 69976 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 373 5 0 5 4.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939571 69976 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 373 5 0 5 4.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
57393713 69998 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 354 5 0 6 3.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939593 69998 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 354 5 0 6 3.6 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
44190556 195978 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 368 5 1 6 3.7 COc1ccc(Nc2nc(C)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
CHEMBL559765 195978 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 368 5 1 6 3.7 COc1ccc(Nc2nc(C)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
42618166 172942 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 339 6 1 6 4.0 CCC(CC)Nc1nc(C)nc2c(-c3ccc(OC)cc3)c(C)nn12 10.1021/jm9000242
CHEMBL451693 172942 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 339 6 1 6 4.0 CCC(CC)Nc1nc(C)nc2c(-c3ccc(OC)cc3)c(C)nn12 10.1021/jm9000242
24180501 94477 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 386 6 0 4 6.4 CCCC(CCC)n1cc2c3c(nc(C)cc31)N(c1ccc(C#N)cc1C)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL251386 94477 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 386 6 0 4 6.4 CCCC(CCC)n1cc2c3c(nc(C)cc31)N(c1ccc(C#N)cc1C)CC2 10.1016/j.bmcl.2007.06.077
24768328 97706 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 391 7 3 5 4.0 CC[C@@H](CO)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C(=O)NC 10.1021/jm070579c
CHEMBL271370 97706 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 391 7 3 5 4.0 CC[C@@H](CO)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C(=O)NC 10.1021/jm070579c
3663 99967 83 None - 29 Human 6.5 pIC50 = 6.5 Binding
Inhibition of CRF1 receptorInhibition of CRF1 receptor
ChEMBL 504 0 6 8 5.1 Cc1cc(O)c2c(=O)c3c(O)cc(O)c4c5c(O)cc(O)c6c(=O)c7c(O)cc(C)c8c1c2c(c34)c(c78)c65 10.1021/np1000329
CHEMBL286494 99967 83 None - 29 Human 6.5 pIC50 = 6.5 Binding
Inhibition of CRF1 receptorInhibition of CRF1 receptor
ChEMBL 504 0 6 8 5.1 Cc1cc(O)c2c(=O)c3c(O)cc(O)c4c5c(O)cc(O)c6c(=O)c7c(O)cc(C)c8c1c2c(c34)c(c78)c65 10.1021/np1000329
54585866 60657 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 398 8 0 7 3.6 CCCN(CCC)c1nc2c(c(-c3ccc(OC)cc3OC)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760261 60657 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 398 8 0 7 3.6 CCCN(CCC)c1nc2c(c(-c3ccc(OC)cc3OC)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
54579975 60658 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 474 6 0 5 5.6 CCCN(CCC)c1nc2c(c(-c3ccc(C(F)(F)F)cc3C(F)(F)F)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760262 60658 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 474 6 0 5 5.6 CCCN(CCC)c1nc2c(c(-c3ccc(C(F)(F)F)cc3C(F)(F)F)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
11250707 12267 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 522 8 1 6 4.6 CCN(CCCS(C)(=O)=O)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1021/jm049737f
CHEMBL1184720 12267 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 522 8 1 6 4.6 CCN(CCCS(C)(=O)=O)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1021/jm049737f
CHEMBL365488 12267 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 522 8 1 6 4.6 CCN(CCCS(C)(=O)=O)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1021/jm049737f
56666769 65308 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 441 9 1 6 6.4 CCCN(CCC)c1c(C2CCCC2)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828894 65308 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 441 9 1 6 6.4 CCCN(CCC)c1c(C2CCCC2)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
11247672 174906 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 440 4 1 7 2.2 COc1ccc(N2CCc3c(-n4ccc(N5CCNS5(=O)=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL456449 174906 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 440 4 1 7 2.2 COc1ccc(N2CCc3c(-n4ccc(N5CCNS5(=O)=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
58223435 127870 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 461 11 0 9 4.2 COCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCC1 nan
CHEMBL3664583 127870 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 461 11 0 9 4.2 COCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCC1 nan
22177839 64737 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 380 6 1 6 4.6 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCO2 10.1016/j.bmc.2011.07.055
CHEMBL1819061 64737 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 380 6 1 6 4.6 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCO2 10.1016/j.bmc.2011.07.055
46881865 8011 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 395 8 1 9 2.4 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(C)nc(OC)nc2OC)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1090739 8011 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 395 8 1 9 2.4 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(C)nc(OC)nc2OC)c1=O 10.1016/j.bmcl.2010.01.129
24768328 97706 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 391 7 3 5 4.0 CC[C@@H](CO)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C(=O)NC 10.1021/jm070579c
CHEMBL271370 97706 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 391 7 3 5 4.0 CC[C@@H](CO)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C(=O)NC 10.1021/jm070579c
56680359 65311 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 401 9 0 6 5.2 CCCN(CCC)c1cc(N(CC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828897 65311 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 401 9 0 6 5.2 CCCN(CCC)c1cc(N(CC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
10180350 63407 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 418 6 0 4 6.5 CCCC(CCC)N1CCC2CN(c3ccc(Cl)cc3Cl)c3nc(C)nc1c32 10.1016/j.bmcl.2007.06.077
CHEMBL179608 63407 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 418 6 0 4 6.5 CCCC(CCC)N1CCC2CN(c3ccc(Cl)cc3Cl)c3nc(C)nc1c32 10.1016/j.bmcl.2007.06.077
21912361 98039 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 331 6 0 3 5.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(F)cc2C)c1C 10.1021/jm070578k
CHEMBL273068 98039 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 331 6 0 3 5.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(F)cc2C)c1C 10.1021/jm070578k
54580963 60656 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 428 9 0 8 3.6 CCCN(CCC)c1nc2c(c(-c3c(OC)cc(OC)cc3OC)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760260 60656 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 428 9 0 8 3.6 CCCN(CCC)c1nc2c(c(-c3c(OC)cc(OC)cc3OC)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
57395432 69983 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 337 5 0 4 5.2 CCC(CC)c1nc(C)c2nc(-c3ccc(OC)cc3C)c(C)cn12 10.1016/j.bmc.2011.11.015
CHEMBL1939578 69983 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 337 5 0 4 5.2 CCC(CC)c1nc(C)c2nc(-c3ccc(OC)cc3C)c(C)cn12 10.1016/j.bmc.2011.11.015
24768337 166015 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 429 9 1 8 3.1 CCCN(CCOC)c1nc(C)nc2c1NC(=O)CN2c1cc(OC)c(OC)cc1C 10.1021/jm0611410
CHEMBL425476 166015 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 429 9 1 8 3.1 CCCN(CCOC)c1nc(C)nc2c1NC(=O)CN2c1cc(OC)c(OC)cc1C 10.1021/jm0611410
11235455 175466 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 418 5 1 6 3.5 CCOc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL457710 175466 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 418 5 1 6 3.5 CCOc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
44589349 176117 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 367 3 0 7 3.3 Cc1cc(C#N)ccc1N1CCc2c(-n3ccc(-n4cccn4)n3)ccnc21 10.1021/jm800743q
CHEMBL459181 176117 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 367 3 0 7 3.3 Cc1cc(C#N)ccc1N1CCc2c(-n3ccc(-n4cccn4)n3)ccnc21 10.1021/jm800743q
53358606 130593 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 386 4 1 4 4.1 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2cc3c(n2)CCCC3)CC1 nan
CHEMBL3681376 130593 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 386 4 1 4 4.1 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2cc3c(n2)CCCC3)CC1 nan
58223385 127855 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 13 0 9 4.5 CCOCc1cc(OC)c(-c2csc3c(N(CCOC)CC4CC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664568 127855 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 13 0 9 4.5 CCOCc1cc(OC)c(-c2csc3c(N(CCOC)CC4CC4)c(OC)nn23)c(OC)c1 nan
58223464 127862 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 501 11 0 9 5.0 CCOCc1cc(OC)c(-c2csc3c(N(CC4CCC4)C4CCOC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664575 127862 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 501 11 0 9 5.0 CCOCc1cc(OC)c(-c2csc3c(N(CC4CCC4)C4CCOC4)c(OC)nn23)c(OC)c1 nan
56663335 65305 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 415 10 1 6 5.7 CCCc1c(Nc2ccc(OC)cc2Cl)nc2ccnn2c1N(CCC)CCC 10.1016/j.bmc.2011.08.055
CHEMBL1828891 65305 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 415 10 1 6 5.7 CCCc1c(Nc2ccc(OC)cc2Cl)nc2ccnn2c1N(CCC)CCC 10.1016/j.bmc.2011.08.055
21912361 98039 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 331 6 0 3 5.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(F)cc2C)c1C 10.1021/jm070578k
CHEMBL273068 98039 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 331 6 0 3 5.8 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(F)cc2C)c1C 10.1021/jm070578k
11948286 156669 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting method
ChEMBL 410 5 0 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4069551 156669 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting method
ChEMBL 410 5 0 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
11201828 175952 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 453 3 1 6 3.7 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(C#N)cc1C(F)(F)F)CC2 10.1021/jm800744m
CHEMBL458810 175952 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 453 3 1 6 3.7 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(C#N)cc1C(F)(F)F)CC2 10.1021/jm800744m
42618212 184092 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 395 7 0 7 4.1 CCCCN(CC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL482542 184092 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 395 7 0 7 4.1 CCCCN(CC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
57786096 165095 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 475 4 0 6 5.8 Cc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4227177 165095 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 475 4 0 6 5.8 Cc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
70686154 75587 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 466 9 0 7 5.5 CCN(c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12)C1CCOCC1 10.1016/j.bmcl.2012.05.066
CHEMBL2046530 75587 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 466 9 0 7 5.5 CCN(c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12)C1CCOCC1 10.1016/j.bmcl.2012.05.066
11476167 189704 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 439 4 0 7 3.1 COc1ccc(N2CCc3c(-n4ccc(N5CCCS5(=O)=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL515503 189704 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 439 4 0 7 3.1 COc1ccc(N2CCc3c(-n4ccc(N5CCCS5(=O)=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
10184943 66702 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 490 5 0 4 6.6 CCc1nc2c(n1Cc1ccc(-c3ccccc3)cc1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL185541 66702 0 None - 0 Rat 6.5 pIC50 = 6.5 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 490 5 0 4 6.6 CCc1nc2c(n1Cc1ccc(-c3ccccc3)cc1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
58223455 124424 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 457 9 0 8 4.7 COc1cc(C)cc(OC)c1-c1csc2c(N(CC3CC3)CC3CCOC3)c(OC)nn12 nan
CHEMBL3639634 124424 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 457 9 0 8 4.7 COc1cc(C)cc(OC)c1-c1csc2c(N(CC3CC3)CC3CCOC3)c(OC)nn12 nan
58223403 127872 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 483 10 0 8 5.2 COc1cc(C2CC2)cc(OC)c1-c1csc2c(N(CC3CC3)CC3CCOC3)c(OC)nn12 nan
CHEMBL3664585 127872 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 483 10 0 8 5.2 COc1cc(C2CC2)cc(OC)c1-c1csc2c(N(CC3CC3)CC3CCOC3)c(OC)nn12 nan
58223493 127891 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 468 10 0 9 5.2 CCCN(c1ccccn1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664603 127891 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 468 10 0 9 5.2 CCCN(c1ccccn1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
56683762 65500 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 388 8 0 7 4.2 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830518 65500 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 388 8 0 7 4.2 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
46890979 6839 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 352 4 1 5 4.3 Cc1nc(Nc2c(C)cc(Cl)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1084025 6839 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 352 4 1 5 4.3 Cc1nc(Nc2c(C)cc(Cl)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
46891189 6888 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 397 4 1 6 4.2 Cc1nc(Nc2cc(C(F)(F)F)c(C#N)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1084242 6888 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 397 4 1 6 4.2 Cc1nc(Nc2cc(C(F)(F)F)c(C#N)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
54586829 60654 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 380 6 0 5 4.5 CCCN(CCC)c1nc2c(c(-c3ccc(C)cc3C)c(C)n2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760258 60654 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 380 6 0 5 4.5 CCCN(CCC)c1nc2c(c(-c3ccc(C)cc3C)c(C)n2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
21984580 77552 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 433 8 0 5 5.6 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CC1)CC1CCCO1 10.1021/jm300259r
CHEMBL2087560 77552 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 433 8 0 5 5.6 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CC1)CC1CCCO1 10.1021/jm300259r
60155991 77579 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 515 12 0 9 4.8 COCCN(CC1CCOCC1)c1c(SC)nn2c(-c3c(OC)cc(COC)cc3OC)cccc12 10.1021/jm300259r
CHEMBL2087801 77579 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 515 12 0 9 4.8 COCCN(CC1CCOCC1)c1c(SC)nn2c(-c3c(OC)cc(COC)cc3OC)cccc12 10.1021/jm300259r
45273018 196527 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 381 6 0 5 4.7 CCN(c1c(Cl)cc(OC)cc1Cl)c1nccn([C@H](C)C2CC2)c1=O 10.1021/jm900301y
CHEMBL563618 196527 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 381 6 0 5 4.7 CCN(c1c(Cl)cc(OC)cc1Cl)c1nccn([C@H](C)C2CC2)c1=O 10.1021/jm900301y
44589302 189788 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 425 5 0 7 5.0 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)F)c1 10.1021/jm800743q
CHEMBL516175 189788 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 425 5 0 7 5.0 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)F)c1 10.1021/jm800743q
56677029 65307 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 429 11 1 6 6.1 CCCCc1c(Nc2ccc(OC)cc2Cl)nc2ccnn2c1N(CCC)CCC 10.1016/j.bmc.2011.08.055
CHEMBL1828893 65307 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 429 11 1 6 6.1 CCCCc1c(Nc2ccc(OC)cc2Cl)nc2ccnn2c1N(CCC)CCC 10.1016/j.bmc.2011.08.055
10379 3059 39 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1016/j.bmc.2016.11.011
9884366 3059 39 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1016/j.bmc.2016.11.011
CHEMBL482950 3059 39 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1016/j.bmc.2016.11.011
DB12572 3059 39 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by [125I]-CRF addition measured after 1 hr by liquid scintillation counting method
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1016/j.bmc.2016.11.011
24805438 98009 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Inhibition of CRF1 receptorInhibition of CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(CC)Oc1nc(C)cc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
CHEMBL272893 98009 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Inhibition of CRF1 receptorInhibition of CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(CC)Oc1nc(C)cc(Oc2c(C)cc(C)cc2C)c1C 10.1021/jm070578k
44589221 175645 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 375 3 1 7 4.1 Cc1cc(O)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
CHEMBL458115 175645 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 375 3 1 7 4.1 Cc1cc(O)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
58223394 127857 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 14 0 9 4.9 CCOCc1cc(OC)c(-c2csc3c(N(CCCOC)CC4CC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664570 127857 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 14 0 9 4.9 CCOCc1cc(OC)c(-c2csc3c(N(CCCOC)CC4CC4)c(OC)nn23)c(OC)c1 nan
54582098 61042 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 388 9 0 8 2.6 COCCN(CCCF)c1nc(C)nc2c(-c3ccc(OC)nc3)c(C)nn12 10.1016/j.bmcl.2011.02.050
CHEMBL1762823 61042 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 388 9 0 8 2.6 COCCN(CCCF)c1nc(C)nc2c(-c3ccc(OC)nc3)c(C)nn12 10.1016/j.bmcl.2011.02.050
10075105 77566 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 511 11 0 8 5.5 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087574 77566 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 511 11 0 8 5.5 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
9970050 64740 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 380 6 1 6 4.7 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)COC2 10.1016/j.bmc.2011.07.055
CHEMBL1819064 64740 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 380 6 1 6 4.7 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)COC2 10.1016/j.bmc.2011.07.055
44190055 196093 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 347 5 2 5 3.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@@H](CO)C3CC3)c2=O)c(C)c1 10.1021/jm900301y
CHEMBL560823 196093 0 None - 0 Rat 7.5 pIC50 = 7.5 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 347 5 2 5 3.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@@H](CO)C3CC3)c2=O)c(C)c1 10.1021/jm900301y
53357140 130591 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 554 7 3 4 7.1 COc1ccc(-c2c(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)n[nH]c2C)c(Cl)c1 nan
CHEMBL3681374 130591 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 554 7 3 4 7.1 COc1ccc(-c2c(NC[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)n[nH]c2C)c(Cl)c1 nan
145968888 165158 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc([C@H](OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4228089 165158 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc([C@H](OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
58223459 127866 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 12 0 9 4.5 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC(C)OC)c(OC)nn23)c(OC)c1 nan
CHEMBL3664579 127866 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 12 0 9 4.5 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC(C)OC)c(OC)nn23)c(OC)c1 nan
58223427 127892 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 468 10 0 9 5.2 CCCN(c1cccnc1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664604 127892 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 468 10 0 9 5.2 CCCN(c1cccnc1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
44191107 194804 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 367 5 1 5 4.6 COc1cc(Cl)c(C)cc1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900302q
CHEMBL538866 194804 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 367 5 1 5 4.6 COc1cc(Cl)c(C)cc1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1021/jm900302q
57786134 165122 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 387 4 0 3 6.1 CCN(CC)c1cccc2nc3n(c12)CCCC3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4227554 165122 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 387 4 0 3 6.1 CCN(CC)c1cccc2nc3n(c12)CCCC3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
44589291 175482 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 454 5 1 9 2.9 COc1cc(-n2cccn2)ccc1N1CCc2c(-n3ccc(-n4cc[nH]c4=O)n3)cc(C)nc21 10.1021/jm800744m
CHEMBL457742 175482 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 454 5 1 9 2.9 COc1cc(-n2cccn2)ccc1N1CCc2c(-n3ccc(-n4cc[nH]c4=O)n3)cc(C)nc21 10.1021/jm800744m
44589330 175479 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 398 3 0 6 4.5 N#Cc1ccc(N2CCc3c(-n4ccc(-c5ccccn5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
CHEMBL457740 175479 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 398 3 0 6 4.5 N#Cc1ccc(N2CCc3c(-n4ccc(-c5ccccn5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
90654069 128815 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 461 9 2 9 3.3 CCc1sc2c(NC(=O)C3(O)CC3)c(OC)nn2c1-c1c(OC)cc(COC)cc1OC nan
CHEMBL3669433 128815 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 461 9 2 9 3.3 CCc1sc2c(NC(=O)C3(O)CC3)c(OC)nn2c1-c1c(OC)cc(COC)cc1OC nan
10177704 64736 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 378 6 1 5 5.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819060 64736 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 378 6 1 5 5.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
10178898 64741 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 396 6 1 6 5.4 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CSC2 10.1016/j.bmc.2011.07.055
CHEMBL1819065 64741 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 396 6 1 6 5.4 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CSC2 10.1016/j.bmc.2011.07.055
10222795 64757 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 402 5 1 4 6.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(Cl)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819082 64757 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 402 5 1 4 6.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(Cl)cc4Cl)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
11751039 175880 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 440 4 1 7 3.3 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(-n3cccn3)cc1C)CC2 10.1021/jm800744m
CHEMBL458626 175880 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 440 4 1 7 3.3 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(-n3cccn3)cc1C)CC2 10.1021/jm800744m
21984783 77551 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 433 8 0 5 5.4 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CC1)CC1CCOC1 10.1021/jm300259r
CHEMBL2087559 77551 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 433 8 0 5 5.4 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CC1)CC1CCOC1 10.1021/jm300259r
10135080 64749 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 391 6 1 5 5.2 CCC(CC)Nc1c2c(nc3c(-c4ccc(N(C)C)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819073 64749 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 391 6 1 5 5.2 CCC(CC)Nc1c2c(nc3c(-c4ccc(N(C)C)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
42618205 180170 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 353 5 0 6 3.9 CCN(CC)c1nc(C)nc2c(-c3ccc(OC)c(C)c3C)c(C)nn12 10.1021/jm9000242
CHEMBL474906 180170 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 353 5 0 6 3.9 CCN(CC)c1nc(C)nc2c(-c3ccc(OC)c(C)c3C)c(C)nn12 10.1021/jm9000242
54582962 60652 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 364 2 0 5 3.9 Cc1cc(C)c(-c2cn(C)c3nc(N4CCCCC4)n(C)c(=O)c23)c(C)c1 10.1016/j.bmcl.2011.02.086
CHEMBL1760256 60652 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 364 2 0 5 3.9 Cc1cc(C)c(-c2cn(C)c3nc(N4CCCCC4)n(C)c(=O)c23)c(C)c1 10.1016/j.bmcl.2011.02.086
10296796 63761 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 436 7 0 4 6.5 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)C(C)N2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL180151 63761 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 436 7 0 4 6.5 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)C(C)N2c1ccc(Cl)cc1Cl 10.1021/jm049787k
44589278 175465 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 501 5 0 10 2.9 CS(=O)(=O)c1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(S(C)(=O)=O)c1 10.1021/jm800743q
CHEMBL457708 175465 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 501 5 0 10 2.9 CS(=O)(=O)c1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(S(C)(=O)=O)c1 10.1021/jm800743q
58223475 127831 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 463 11 0 8 5.9 CCCN(CCC)c1c(C)nn2c(-c3c(OC)cc(COC)cc3OC)c(SC)sc12 nan
CHEMBL3664544 127831 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 463 11 0 8 5.9 CCCN(CCC)c1c(C)nn2c(-c3c(OC)cc(COC)cc3OC)c(SC)sc12 nan
58223398 127873 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 471 9 0 8 5.4 CCCN(c1c(OC)nn2c(-c3c(OC)cc(C4CC4)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664586 127873 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 471 9 0 8 5.4 CCCN(c1c(OC)nn2c(-c3c(OC)cc(C4CC4)cc3OC)csc12)C1CCOCC1 nan
46891036 7404 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 422 5 1 6 4.9 Cc1nc(Nc2c(Cl)cc(OC(F)(F)F)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1086511 7404 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 422 5 1 6 4.9 Cc1nc(Nc2c(Cl)cc(OC(F)(F)F)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
44189948 195423 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 347 6 1 4 5.0 CCC(CC)Cn1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL552237 195423 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 347 6 1 4 5.0 CCC(CC)Cn1cc(Cl)nc(Nc2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
57786117 165120 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 402 4 0 4 5.3 CCN(CC)c1cccc2nc3n(c12)CCC(=O)N3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4227537 165120 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 402 4 0 4 5.3 CCN(CC)c1cccc2nc3n(c12)CCC(=O)N3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
3499 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.bmcl.2007.06.077
9909468 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.bmcl.2007.06.077
CHEMBL44698 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.bmcl.2007.06.077
44444314 94257 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 395 7 0 4 6.3 CCCC(CCC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)c(F)c1)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL250182 94257 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 395 7 0 4 6.3 CCCC(CCC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)c(F)c1)CC2 10.1016/j.bmcl.2007.06.077
44444336 94494 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 374 5 0 5 4.8 CCC(COC)n1cc2c3c(nc(C)cc31)N(c1ccc(C#N)cc1C)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL251551 94494 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 374 5 0 5 4.8 CCC(COC)n1cc2c3c(nc(C)cc31)N(c1ccc(C#N)cc1C)CC2 10.1016/j.bmcl.2007.06.077
3499 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm800744m
9909468 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm800744m
CHEMBL44698 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm800744m
3499 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm800743q
9909468 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm800743q
CHEMBL44698 1448 28 None - 1 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm800743q
44589328 189741 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 444 4 0 8 4.5 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)(F)F)n1 10.1021/jm800743q
CHEMBL515843 189741 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 444 4 0 8 4.5 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)(F)F)n1 10.1021/jm800743q
21912363 97501 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 4 5.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C=O)cc2C)c1C 10.1021/jm070578k
CHEMBL270343 97501 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 4 5.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C=O)cc2C)c1C 10.1021/jm070578k
21912239 97707 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 7 1 4 5.9 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C(C)(C)O)cc2C)c1C 10.1021/jm070578k
CHEMBL271373 97707 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 7 1 4 5.9 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C(C)(C)O)cc2C)c1C 10.1021/jm070578k
54581053 61043 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 389 9 0 9 2.0 COCCN(CCCF)c1nc(C)nc2c(-c3cnc(OC)nc3)c(C)nn12 10.1016/j.bmcl.2011.02.050
CHEMBL1762824 61043 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 389 9 0 9 2.0 COCCN(CCCF)c1nc(C)nc2c(-c3cnc(OC)nc3)c(C)nn12 10.1016/j.bmcl.2011.02.050
71451516 81523 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 454 11 0 7 4.9 CCN(CCOC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160172 81523 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 454 11 0 7 4.9 CCN(CCOC)c1ccc(OC)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
10376 2930 4 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
9801039 2930 4 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
CHEMBL1819077 2930 4 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
42618202 189767 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 433 6 0 7 4.0 CCN(CC)c1nc(C)nc2c(-c3cc(OC)c(OC)cc3Br)c(C)nn12 10.1021/jm9000242
CHEMBL516026 189767 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 433 6 0 7 4.0 CCN(CC)c1nc(C)nc2c(-c3cc(OC)c(OC)cc3Br)c(C)nn12 10.1021/jm9000242
71455126 81989 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 395 8 1 6 4.2 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OCF)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL2165195 81989 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 395 8 1 6 4.2 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OCF)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
44190825 195146 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 425 4 1 4 5.9 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL550215 195146 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 425 4 1 4 5.9 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
11948286 156669 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 410 5 0 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4069551 156669 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 410 5 0 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
11363701 67414 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 482 6 1 5 6.0 CCN(Cc1ccco1)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1021/jm049737f
CHEMBL188858 67414 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 482 6 1 5 6.0 CCN(Cc1ccco1)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1021/jm049737f
54754516 65304 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 401 9 1 6 5.3 CCCN(CCC)c1c(CC)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828890 65304 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 401 9 1 6 5.3 CCCN(CCC)c1c(CC)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
9908904 180487 4 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm200365y
CHEMBL474287 180487 4 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm200365y
CHEMBL475306 180487 4 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm200365y
57402456 70009 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 353 4 0 5 4.1 CCC(C)c1cc(C)n2nc(-c3c(C)cc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939603 70009 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 353 4 0 5 4.1 CCC(C)c1cc(C)n2nc(-c3c(C)cc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
24768329 85606 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 368 7 1 5 4.9 CCCCN(CC)c1cc(C)nc2c1NCCN2c1ccc(OC)cc1C 10.1021/jm0611410
CHEMBL228227 85606 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 368 7 1 5 4.9 CCCCN(CC)c1cc(C)nc2c1NCCN2c1ccc(OC)cc1C 10.1021/jm0611410
3499 1448 28 None - 1 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm9000242
9909468 1448 28 None - 1 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm9000242
CHEMBL44698 1448 28 None - 1 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm9000242
9908904 180487 4 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL474287 180487 4 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL475306 180487 4 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
11181033 11774 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 383 7 1 6 3.8 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1C 10.1021/jm049737f
CHEMBL1181692 11774 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 383 7 1 6 3.8 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1C 10.1021/jm049737f
CHEMBL188861 11774 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 383 7 1 6 3.8 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1C 10.1021/jm049737f
44591727 191471 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 381 7 0 6 4.7 CCCCN(CC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL519339 191471 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 381 7 0 6 4.7 CCCCN(CC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3C)c(C)nn12 10.1021/jm9000242
56961969 81996 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 443 9 1 7 3.5 COCC(COC)n1cc(Br)nc(Nc2c(C)cc(OCF)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL2165201 81996 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 443 9 1 7 3.5 COCC(COC)n1cc(Br)nc(Nc2c(C)cc(OCF)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
44191186 195615 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 414 6 1 6 4.7 C[C@H](C1CC1)n1cc(C#N)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL556089 195615 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 414 6 1 6 4.7 C[C@H](C1CC1)n1cc(C#N)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1021/jm900302q
56683688 65314 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 413 10 0 6 5.3 C=CCN(c1cc(N(CCC)CCC)n2nccc2n1)c1ccc(OC)cc1Cl 10.1016/j.bmc.2011.08.055
CHEMBL1828900 65314 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 413 10 0 6 5.3 C=CCN(c1cc(N(CCC)CCC)n2nccc2n1)c1ccc(OC)cc1Cl 10.1016/j.bmc.2011.08.055
57398970 69990 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 403 7 1 6 4.0 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(CCO)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939585 69990 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 403 7 1 6 4.0 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(CCO)c(=O)c12 10.1016/j.bmc.2011.11.015
46891493 6565 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 434 8 1 7 4.2 COC[C@H](C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1083012 6565 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 434 8 1 7 4.2 COC[C@H](C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
9820671 188818 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 369 6 1 7 3.9 CC[C@@H](C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL506214 188818 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 369 6 1 7 3.9 CC[C@@H](C)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
71580313 88438 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 424 8 1 6 4.4 Cc1cc(C#N)cc(Cl)c1Nc1nc(Cl)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
CHEMBL2349564 88438 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 424 8 1 6 4.4 Cc1cc(C#N)cc(Cl)c1Nc1nc(Cl)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
57397279 69999 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC(F)F)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939594 69999 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3ccc(OC(F)F)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
10379 3059 39 None - 1 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cellsDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cells
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
9884366 3059 39 None - 1 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cellsDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cells
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
CHEMBL482950 3059 39 None - 1 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cellsDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cells
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
DB12572 3059 39 None - 1 Human 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cellsDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in human IMR32 cells
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
42618222 179633 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 1 7 3.7 CCC[C@H](C)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL474289 179633 0 None - 0 Rat 8.4 pIC50 = 8.4 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 1 7 3.7 CCC[C@H](C)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
57395433 69988 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 387 6 0 5 5.1 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(CC)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939583 69988 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 387 6 0 5 5.1 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(CC)c(=O)c12 10.1016/j.bmc.2011.11.015
44190341 196124 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 373 6 0 4 5.3 CC[C@H](C1CC1)n1cc(Cl)nc(N(CC)c2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL561035 196124 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 373 6 0 4 5.3 CC[C@H](C1CC1)n1cc(Cl)nc(N(CC)c2c(C)cc(C)cc2C)c1=O 10.1021/jm900301y
9908904 180487 4 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL474287 180487 4 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL475306 180487 4 None - 0 Human 8.3 pIC50 = 8.3 Binding
Binding affinity to CRF1 receptor in human IMR32 cellsBinding affinity to CRF1 receptor in human IMR32 cells
ChEMBL 399 9 0 8 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
56659949 65508 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 381 6 1 5 6.0 CCc1cc(Cl)ccc1Nc1nc2ccnn2c2c1ccn2C(CC)CC 10.1016/j.bmc.2011.08.055
CHEMBL1830525 65508 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 381 6 1 5 6.0 CCc1cc(Cl)ccc1Nc1nc2ccnn2c2c1ccn2C(CC)CC 10.1016/j.bmc.2011.08.055
71580427 88444 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 346 6 1 6 3.2 COc1nc(C)c(Nc2nc(C)cn([C@@H](CF)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2013.02.009
CHEMBL2349571 88444 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 346 6 1 6 3.2 COc1nc(C)c(Nc2nc(C)cn([C@@H](CF)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2013.02.009
58280028 139923 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 463 10 2 8 4.1 CCCCNC(=O)OC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
CHEMBL3799560 139923 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 463 10 2 8 4.1 CCCCNC(=O)OC[C@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2016.03.067
46881836 7744 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 414 8 1 7 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1089038 7744 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 414 8 1 7 3.9 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cc(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.01.129
44191108 196681 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 331 4 1 4 4.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900302q
CHEMBL564639 196681 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 331 4 1 4 4.5 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1C 10.1021/jm900302q
57400682 70002 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 359 4 0 5 4.2 CCC(C)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939597 70002 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 359 4 0 5 4.2 CCC(C)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
127046470 139618 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 469 8 1 9 3.9 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)c3ccncc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3797551 139618 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 469 8 1 9 3.9 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)c3ccncc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
42618234 188276 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 368 7 0 7 3.7 CCCCN(CC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL500013 188276 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 368 7 0 7 3.7 CCCCN(CC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
42618186 179996 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 6 0 7 3.4 C=CCN(C)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL474699 179996 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 6 0 7 3.4 C=CCN(C)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
42618203 179252 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 493 10 0 9 3.3 COCCN(CCOC)c1nc(C)nc2c(-c3cc(OC)c(OC)cc3Br)c(C)nn12 10.1021/jm9000242
CHEMBL472874 179252 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 493 10 0 9 3.3 COCCN(CCOC)c1nc(C)nc2c(-c3cc(OC)c(OC)cc3Br)c(C)nn12 10.1021/jm9000242
58223391 127846 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 463 13 0 9 4.5 CCCCN(CCOC)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664559 127846 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 463 13 0 9 4.5 CCCCN(CCOC)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
60155710 77555 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 463 9 0 6 5.5 CCc1nn2c(-c3c(C)cc(OC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087563 77555 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 463 9 0 6 5.5 CCc1nn2c(-c3c(C)cc(OC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
60155795 77563 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 451 9 0 6 5.5 CCCN(CC1CCOCC1)c1c(CC)nn2c(-c3c(OC)cc(C)cc3OC)cccc12 10.1021/jm300259r
CHEMBL2087571 77563 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 451 9 0 6 5.5 CCCN(CC1CCOCC1)c1c(CC)nn2c(-c3c(OC)cc(C)cc3OC)cccc12 10.1021/jm300259r
21912363 97501 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 4 5.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C=O)cc2C)c1C 10.1021/jm070578k
CHEMBL270343 97501 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 4 5.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C=O)cc2C)c1C 10.1021/jm070578k
21912239 97707 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 7 1 4 5.9 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C(C)(C)O)cc2C)c1C 10.1021/jm070578k
CHEMBL271373 97707 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 7 1 4 5.9 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C(C)(C)O)cc2C)c1C 10.1021/jm070578k
53358377 124446 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 388 5 1 4 4.7 Cc1cc(C(C)C)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
CHEMBL3639802 124446 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 388 5 1 4 4.7 Cc1cc(C(C)C)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
11383860 67023 0 None - 1 Human 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 394 7 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm040058e
CHEMBL187039 67023 0 None - 1 Human 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 394 7 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm040058e
21984555 77549 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 407 9 0 5 5.1 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CCOC)CC1CC1 10.1021/jm300259r
CHEMBL2087557 77549 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 407 9 0 5 5.1 CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CCOC)CC1CC1 10.1021/jm300259r
71455051 81513 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 444 9 0 5 6.2 CCN(CC)c1ccc(C(F)F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160162 81513 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 444 9 0 5 6.2 CCN(CC)c1ccc(C(F)F)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
56670201 65312 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 415 10 0 6 5.6 CCCN(CCC)c1cc(N(CCC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828898 65312 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 415 10 0 6 5.6 CCCN(CCC)c1cc(N(CCC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56659947 65498 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 374 7 1 7 4.2 CCC(CC)Nc1cc(N(C)c2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830516 65498 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 374 7 1 7 4.2 CCC(CC)Nc1cc(N(C)c2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
56663414 65504 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 401 9 0 6 5.2 CCCN(CCC)c1cc(N(CC)c2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
CHEMBL1830521 65504 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 401 9 0 6 5.2 CCCN(CCC)c1cc(N(CC)c2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
58730488 77556 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 479 10 0 7 5.2 CCc1nn2c(-c3c(OC)cc(OC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087564 77556 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 479 10 0 7 5.2 CCc1nn2c(-c3c(OC)cc(OC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
25150449 175761 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 401 4 0 7 5.0 COc1ccc(-n2ccc3c(-n4ccc(-c5nccs5)n4)cc(C)nc32)c(C)c1 10.1021/jm800743q
CHEMBL458353 175761 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 401 4 0 7 5.0 COc1ccc(-n2ccc3c(-n4ccc(-c5nccs5)n4)cc(C)nc32)c(C)c1 10.1021/jm800743q
58223397 127845 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 457 8 0 8 4.8 COc1cc(C)cc(OC)c1-c1csc2c(N(CC3CC3)C3CCOCC3)c(OC)nn12 nan
CHEMBL3664558 127845 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 457 8 0 8 4.8 COc1cc(C)cc(OC)c1-c1csc2c(N(CC3CC3)C3CCOCC3)c(OC)nn12 nan
71462615 82604 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 487 11 0 9 4.6 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCCO4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179182 82604 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 487 11 0 9 4.6 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCCO4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
24768335 85492 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 428 9 1 7 3.7 CCCN(CCOC)c1cc(C)nc2c1NC(=O)CN2c1cc(OC)c(OC)cc1C 10.1021/jm0611410
CHEMBL227028 85492 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 428 9 1 7 3.7 CCCN(CCOC)c1cc(C)nc2c1NC(=O)CN2c1cc(OC)c(OC)cc1C 10.1021/jm0611410
10202622 123822 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 424 7 0 5 4.9 CCCC(COC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL362413 123822 0 None - 0 Rat 7.4 pIC50 = 7.4 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 424 7 0 5 4.9 CCCC(COC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
58223445 127843 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 471 10 0 8 4.9 CCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCOC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664556 127843 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 471 10 0 8 4.9 CCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCOC4)c(OC)nn23)c(OC)c1 nan
58896479 176269 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 496 6 1 5 8.1 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(CC(C)(C)C)c3ccc(Cl)cc3)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4566348 176269 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 496 6 1 5 8.1 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(CC(C)(C)C)c3ccc(Cl)cc3)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4595038 176269 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 496 6 1 5 8.1 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(CC(C)(C)C)c3ccc(Cl)cc3)c2n1C 10.1016/j.bmc.2016.08.005
145959453 162155 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 370 4 1 7 3.3 CCN(CC)c1nc(C)nc2c1s/c(=N/N)n2-c1c(C)cc(C)cc1C 10.1016/j.ejmech.2017.07.016
CHEMBL4161963 162155 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 370 4 1 7 3.3 CCN(CC)c1nc(C)nc2c1s/c(=N/N)n2-c1c(C)cc(C)cc1C 10.1016/j.ejmech.2017.07.016
58223386 127847 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 487 10 0 9 4.6 COCc1cc(OC)c(-c2csc3c(N(CC4CCC4)C4CCOC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664560 127847 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 487 10 0 9 4.6 COCc1cc(OC)c(-c2csc3c(N(CC4CCC4)C4CCOC4)c(OC)nn23)c(OC)c1 nan
58223431 127858 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 10 0 9 4.5 COCc1cc(OC)c(-c2csc3c(N(CC(C)C)C4CCOC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664571 127858 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 10 0 9 4.5 COCc1cc(OC)c(-c2csc3c(N(CC(C)C)C4CCOC4)c(OC)nn23)c(OC)c1 nan
58223396 127895 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 487 11 0 9 4.3 CCCN(CC1C2COCC21)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664607 127895 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 487 11 0 9 4.3 CCCN(CC1C2COCC21)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
58223461 127896 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 499 11 0 9 4.3 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4C5COCC54)c(OC)nn23)c(OC)c1 nan
CHEMBL3664608 127896 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 499 11 0 9 4.3 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4C5COCC54)c(OC)nn23)c(OC)c1 nan
10182058 65258 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 444 5 0 5 5.0 CCc1nc2c(n1Cc1ccc(OC)cc1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL182779 65258 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 444 5 0 5 5.0 CCc1nc2c(n1Cc1ccc(OC)cc1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
10137474 64606 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 428 4 0 4 5.3 CCc1nc2c(n1Cc1ccccc1C)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL181699 64606 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 428 4 0 4 5.3 CCc1nc2c(n1Cc1ccccc1C)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
51352159 82619 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 485 10 0 8 5.2 COCc1cc(OC)c(-c2csc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 nan
CHEMBL2179197 82619 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 485 10 0 8 5.2 COCc1cc(OC)c(-c2csc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 nan
71455473 82618 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 470 9 0 9 4.7 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(C#N)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179196 82618 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 470 9 0 9 4.7 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(C#N)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
51352159 82619 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 485 10 0 8 5.2 COCc1cc(OC)c(-c2csc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179197 82619 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 485 10 0 8 5.2 COCc1cc(OC)c(-c2csc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 10.1021/jm300864p
57786009 164935 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 507 6 0 8 5.2 COc1nc(C)nc(OC)c1N1CCCn2c1nc1c(Cl)ccc(C(OC(F)F)C(F)(F)F)c12 10.1016/j.bmc.2018.01.020
CHEMBL4224781 164935 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 507 6 0 8 5.2 COc1nc(C)nc(OC)c1N1CCCn2c1nc1c(Cl)ccc(C(OC(F)F)C(F)(F)F)c12 10.1016/j.bmc.2018.01.020
24768323 98050 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 7 0 5 5.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C(=O)OC 10.1021/jm070578k
CHEMBL273117 98050 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 7 0 5 5.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C(=O)OC 10.1021/jm070578k
70692631 75900 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Anatgonist activity at CRF1 receptor (unknown origin)Anatgonist activity at CRF1 receptor (unknown origin)
ChEMBL 378 7 2 4 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)[nH]c12 10.1016/j.ejmech.2021.114085
CHEMBL2049190 75900 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Anatgonist activity at CRF1 receptor (unknown origin)Anatgonist activity at CRF1 receptor (unknown origin)
ChEMBL 378 7 2 4 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)[nH]c12 10.1016/j.ejmech.2021.114085
58223442 127889 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 12 0 9 5.4 CCCCN(c1c(OCC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664601 127889 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 12 0 9 5.4 CCCCN(c1c(OCC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 nan
58223478 128813 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 499 11 0 9 4.8 COCc1cc(OC)c(-c2csc3c(N(CC4=CCOCC4)CC4CC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3669431 128813 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 499 11 0 9 4.8 COCc1cc(OC)c(-c2csc3c(N(CC4=CCOCC4)CC4CC4)c(OC)nn23)c(OC)c1 nan
60155888 77574 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 481 9 0 7 5.7 COc1cc(C)cc(OC)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(SC)nn12 10.1021/jm300259r
CHEMBL2087796 77574 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 481 9 0 7 5.7 COc1cc(C)cc(OC)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(SC)nn12 10.1021/jm300259r
24768323 98050 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 7 0 5 5.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C(=O)OC 10.1021/jm070578k
CHEMBL273117 98050 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 371 7 0 5 5.5 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1C(=O)OC 10.1021/jm070578k
70696716 75906 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 437 11 1 6 6.1 CCCN(CCC)c1cccc2nc(Nc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2049197 75906 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 437 11 1 6 6.1 CCCN(CCC)c1cccc2nc(Nc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
58223502 82605 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 461 12 0 9 4.1 COCCN(CC1CC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL2179183 82605 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 461 12 0 9 4.1 COCCN(CC1CC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
58223374 127860 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 13 0 9 4.5 CCOCCN(CC1CC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664573 127860 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 13 0 9 4.5 CCOCCN(CC1CC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
58223416 127881 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 485 11 0 8 5.8 COCCCN(c1c(OC)nn2c(-c3c(OC)cc(C4CC4)cc3OC)csc12)C1CCCC1 nan
CHEMBL3664593 127881 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 485 11 0 8 5.8 COCCCN(c1c(OC)nn2c(-c3c(OC)cc(C4CC4)cc3OC)csc12)C1CCCC1 nan
71455472 82603 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 487 11 0 9 4.5 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCOC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179181 82603 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 487 11 0 9 4.5 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCOC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
58223502 82605 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 461 12 0 9 4.1 COCCN(CC1CC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 10.1021/jm300864p
CHEMBL2179183 82605 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 461 12 0 9 4.1 COCCN(CC1CC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 10.1021/jm300864p
137656239 158530 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 466 7 2 6 4.9 CCN(CCO)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4091442 158530 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 466 7 2 6 4.9 CCN(CCO)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
44156254 164971 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 476 5 0 6 5.8 COc1ccc(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4225373 164971 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 476 5 0 6 5.8 COc1ccc(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
57786307 165224 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 475 5 0 5 6.4 COc1ccc(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)c1 10.1016/j.bmc.2018.01.020
CHEMBL4229125 165224 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 475 5 0 5 6.4 COc1ccc(N2CCCn3c2nc2c(Cl)ccc(C(OC(F)F)C(F)(F)F)c23)c(C)c1 10.1016/j.bmc.2018.01.020
58223379 127848 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 477 9 0 8 5.0 COc1cc(Cl)cc(OC)c1-c1csc2c(N(CC3CC3)CC3CCOC3)c(OC)nn12 nan
CHEMBL3664561 127848 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 477 9 0 8 5.0 COc1cc(Cl)cc(OC)c1-c1csc2c(N(CC3CC3)CC3CCOC3)c(OC)nn12 nan
9827578 77561 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 507 12 0 7 5.8 CCOCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(CC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087569 77561 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 507 12 0 7 5.8 CCOCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(CC)nn23)c(OC)c1 10.1021/jm300259r
22177864 64753 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 410 7 1 6 5.5 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4SC)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819078 64753 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 410 7 1 6 5.5 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4SC)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
56665181 64760 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 386 6 1 5 5.6 CCC(CC)Nc1c(C)c(C)nc2c(-c3ccc(OC)cc3Cl)c(C)nn12 10.1016/j.bmc.2011.07.055
CHEMBL1819085 64760 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 386 6 1 5 5.6 CCC(CC)Nc1c(C)c(C)nc2c(-c3ccc(OC)cc3Cl)c(C)nn12 10.1016/j.bmc.2011.07.055
53357923 130613 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 461 5 1 3 6.1 CCc1nn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c(C)c1Cl nan
CHEMBL3681396 130613 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 461 5 1 3 6.1 CCc1nn(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)c(C)c1Cl nan
44392688 66315 0 None - 1 Human 7.3 pIC50 = 7.3 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL184930 66315 0 None - 1 Human 7.3 pIC50 = 7.3 Binding
Inhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptorInhibition of CRF-stimulated cAMP production in cells expressing CRF1 receptor
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
11237255 12254 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 380 7 1 4 5.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1 10.1021/jm049737f
CHEMBL1184638 12254 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 380 7 1 4 5.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1 10.1021/jm049737f
CHEMBL361296 12254 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 380 7 1 4 5.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1 10.1021/jm049737f
10112758 64744 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 418 7 1 5 6.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C4CCC4)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819068 64744 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 418 7 1 5 6.1 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C4CCC4)nn13)CCC2 10.1016/j.bmc.2011.07.055
71580315 88440 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 444 8 1 6 4.8 N#Cc1cc(Cl)c(Nc2nc(Cl)cn([C@@H](COCCF)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2013.02.009
CHEMBL2349566 88440 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 444 8 1 6 4.8 N#Cc1cc(Cl)c(Nc2nc(Cl)cn([C@@H](COCCF)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2013.02.009
56961966 81991 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 421 8 1 7 3.8 COCC(COC)n1cc(Cl)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL2165197 81991 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 421 8 1 7 3.8 COCC(COC)n1cc(Cl)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1016/j.bmcl.2012.08.112
57400681 70000 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 339 4 0 5 3.8 CCC(C)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939595 70000 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 339 4 0 5 3.8 CCC(C)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
46891154 7340 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 328 5 1 6 3.3 COc1cc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.04.121
CHEMBL1086233 7340 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 328 5 1 6 3.3 COc1cc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2010.04.121
42618177 184355 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 383 7 1 7 4.3 CCC(CC)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL484408 184355 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 383 7 1 7 4.3 CCC(CC)Nc1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
3496 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm200365y
9862166 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm200365y
CHEMBL270948 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm200365y
42618224 179276 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 368 7 1 7 4.1 CCCCC(C)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL473070 179276 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 368 7 1 7 4.1 CCCCC(C)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
3496 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
9862166 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
CHEMBL270948 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
3496 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
9862166 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
CHEMBL270948 1180 42 None -1 2 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 326 6 1 3 6.0 CCC(Nc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
127047521 140019 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 469 8 1 9 3.9 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)c3cccnc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3800125 140019 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 469 8 1 9 3.9 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)c3cccnc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
25114821 69997 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3cnc(OC(F)F)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939592 69997 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3cnc(OC(F)F)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
127047518 139585 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 406 7 1 8 3.2 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(C)=O)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3797368 139585 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 406 7 1 8 3.2 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(C)=O)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
56961968 81992 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 439 9 1 7 4.1 COCC(COC)n1cc(Cl)nc(Nc2c(Cl)cc(OCF)cc2Cl)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL2165198 81992 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 439 9 1 7 4.1 COCC(COC)n1cc(Cl)nc(Nc2c(Cl)cc(OCF)cc2Cl)c1=O 10.1016/j.bmcl.2012.08.112
9841231 97733 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 347 6 0 3 6.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C 10.1021/jm070578k
CHEMBL271546 97733 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 347 6 0 3 6.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C 10.1021/jm070578k
54584993 61038 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 388 8 0 8 2.5 COCCN(CCF)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1016/j.bmcl.2011.02.050
CHEMBL1762819 61038 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 388 8 0 8 2.5 COCCN(CCF)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1016/j.bmcl.2011.02.050
9841231 97733 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 347 6 0 3 6.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C 10.1021/jm070578k
CHEMBL271546 97733 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 347 6 0 3 6.3 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C 10.1021/jm070578k
3495 1175 28 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm960861b
5311055 1175 28 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm960861b
CHEMBL9946 1175 28 None - 1 Rat 8.3 pIC50 = 8.3 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm960861b
44190559 196154 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 378 5 1 6 3.4 C#Cc1cn([C@H](C)C2CC2)c(=O)c(Nc2ccc(OC)nc2C(F)(F)F)n1 10.1021/jm900301y
CHEMBL561225 196154 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 378 5 1 6 3.4 C#Cc1cn([C@H](C)C2CC2)c(=O)c(Nc2ccc(OC)nc2C(F)(F)F)n1 10.1021/jm900301y
21912379 155706 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 390 6 1 3 6.5 CCC(CC)Nc1cc(C)nc(Oc2c(C)cc(Br)cc2C)c1C 10.1021/jm070579c
CHEMBL405198 155706 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 390 6 1 3 6.5 CCC(CC)Nc1cc(C)nc(Oc2c(C)cc(Br)cc2C)c1C 10.1021/jm070579c
21912379 155706 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 390 6 1 3 6.5 CCC(CC)Nc1cc(C)nc(Oc2c(C)cc(Br)cc2C)c1C 10.1021/jm070579c
CHEMBL405198 155706 0 None - 0 Rat 8.3 pIC50 = 8.3 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 390 6 1 3 6.5 CCC(CC)Nc1cc(C)nc(Oc2c(C)cc(Br)cc2C)c1C 10.1021/jm070579c
57397278 69992 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 379 6 0 5 5.0 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939587 69992 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 379 6 0 5 5.0 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(C3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
42618226 179304 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 368 7 0 7 3.7 CCCN(CCC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL473277 179304 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 368 7 0 7 3.7 CCCN(CCC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
54584992 61037 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 358 6 0 7 2.9 CCN(CCF)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1016/j.bmcl.2011.02.050
CHEMBL1762818 61037 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 358 6 0 7 2.9 CCN(CCF)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1016/j.bmcl.2011.02.050
24768343 142798 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 394 7 1 5 4.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)=O)cc1C 10.1021/jm0611410
CHEMBL389288 142798 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 394 7 1 5 4.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)=O)cc1C 10.1021/jm0611410
44190241 196094 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 351 6 1 6 3.5 COC[C@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL560827 196094 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 351 6 1 6 3.5 COC[C@H](C)n1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
25115057 69993 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 399 6 0 5 5.4 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939588 69993 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 399 6 0 5 5.4 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3Cl)n(C3CC3)c(=O)c12 10.1016/j.bmc.2011.11.015
10255153 77559 8 None - 1 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087549 77559 8 None - 1 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
CHEMBL2087567 77559 8 None - 1 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 493 11 0 7 5.4 CCc1nn2c(-c3c(OC)cc(COC)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1 10.1021/jm300259r
71453734 82601 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 501 11 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCCOC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179179 82601 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 501 11 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCCOC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
57786200 165220 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 499 4 0 4 7.4 FC(F)OC(c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl)C(F)(F)F 10.1016/j.bmc.2018.01.020
CHEMBL4229070 165220 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 499 4 0 4 7.4 FC(F)OC(c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl)C(F)(F)F 10.1016/j.bmc.2018.01.020
58896503 176542 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 484 8 1 6 6.7 COCCN(c1ccc(Cl)cc1)c1cccc2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.08.005
CHEMBL4540030 176542 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 484 8 1 6 6.7 COCCN(c1ccc(Cl)cc1)c1cccc2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.08.005
CHEMBL4597163 176542 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 484 8 1 6 6.7 COCCN(c1ccc(Cl)cc1)c1cccc2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.08.005
10113560 65322 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 430 8 0 4 6.5 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049787k
CHEMBL182914 65322 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 430 8 0 4 6.5 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049787k
3520 3267 54 None 1 2 Human 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm040058e
9821250 3267 54 None 1 2 Human 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm040058e
CHEMBL309138 3267 54 None 1 2 Human 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm040058e
11372928 170270 0 None - 1 Human 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 398 7 0 6 4.5 CCCN(CCC)c1c(F)c(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL444614 170270 0 None - 1 Human 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 398 7 0 6 4.5 CCCN(CCC)c1c(F)c(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
9865060 63543 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 387 6 0 5 5.8 CCCC(CCC)n1cc2c3c(nc(C)nc31)N(c1ccc(C#N)cc1C)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL180025 63543 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 387 6 0 5 5.8 CCCC(CCC)n1cc2c3c(nc(C)nc31)N(c1ccc(C#N)cc1C)CC2 10.1016/j.bmcl.2007.06.077
44444318 94410 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 367 5 0 4 5.5 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)c(F)c1)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL250996 94410 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 367 5 0 4 5.5 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)c(F)c1)CC2 10.1016/j.bmcl.2007.06.077
11475476 174992 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 413 4 1 6 3.2 CCc1cc(C#N)ccc1N1CCc2c(-n3ccc(N4CCNC4=O)n3)cc(C)nc21 10.1021/jm800744m
CHEMBL456660 174992 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 413 4 1 6 3.2 CCc1cc(C#N)ccc1N1CCc2c(-n3ccc(N4CCNC4=O)n3)cc(C)nc21 10.1021/jm800744m
58223494 127833 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 501 11 0 9 4.8 COCc1cc(OC)c(-c2c(C)sc3c(N(CC4CC4)CC4CCOC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664546 127833 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 501 11 0 9 4.8 COCc1cc(OC)c(-c2c(C)sc3c(N(CC4CC4)CC4CCOC4)c(OC)nn23)c(OC)c1 nan
58223415 127838 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 461 10 0 9 4.2 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOC1 nan
CHEMBL3664551 127838 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 461 10 0 9 4.2 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOC1 nan
58223501 127890 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 12 0 9 4.9 CCCN(CC1CCOC1)c1c(OCC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664602 127890 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 12 0 9 4.9 CCCN(CC1CCOC1)c1c(OCC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
58801661 77565 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 495 11 0 8 4.8 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(OC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087573 77565 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 495 11 0 8 4.8 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(OC)nn23)c(OC)c1 10.1021/jm300259r
46890981 6841 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 358 7 1 7 2.9 COCC(C1CC1)n1nc(C)nc(Nc2c(C)cc(OC)cc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1084027 6841 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 358 7 1 7 2.9 COCC(C1CC1)n1nc(C)nc(Nc2c(C)cc(OC)cc2C)c1=O 10.1016/j.bmcl.2010.04.121
11361847 63898 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 408 5 0 4 5.5 CCc1nc2c(n1C(CC)C(C)C)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL180491 63898 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 408 5 0 4 5.5 CCc1nc2c(n1C(CC)C(C)C)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
58223387 127841 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 501 11 0 9 5.0 COc1cc(C(C)OC)cc(OC)c1-c1csc2c(N(CC3CC3)CC3CCOC3)c(OC)nn12 nan
CHEMBL3664554 127841 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 501 11 0 9 5.0 COc1cc(C(C)OC)cc(OC)c1-c1csc2c(N(CC3CC3)CC3CCOC3)c(OC)nn12 nan
58223495 127879 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 473 9 0 9 4.4 COCc1cc(OC)c(-c2csc3c(N(C4CCC4)C4CCOC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664591 127879 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 473 9 0 9 4.4 COCc1cc(OC)c(-c2csc3c(N(C4CCC4)C4CCOC4)c(OC)nn23)c(OC)c1 nan
58223451 127886 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 456 9 0 9 4.4 COCCN(c1c(OC)nn2c(-c3c(OC)cc(C#N)cc3OC)csc12)C1CCCC1 nan
CHEMBL3664598 127886 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 456 9 0 9 4.4 COCCN(c1c(OC)nn2c(-c3c(OC)cc(C#N)cc3OC)csc12)C1CCCC1 nan
58223407 127894 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 480 10 0 9 5.2 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)c4cccnc4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664606 127894 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 480 10 0 9 5.2 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)c4cccnc4)c(OC)nn23)c(OC)c1 nan
60155540 77572 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 490 10 0 8 4.7 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(C#N)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087794 77572 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 490 10 0 8 4.7 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4CC4)c(C#N)nn23)c(OC)c1 10.1021/jm300259r
44237814 82610 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 489 11 0 9 5.0 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179188 82610 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 489 11 0 9 5.0 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
155553483 174191 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 508 7 1 6 7.0 COc1cccc(N(c2cccc3nc(Nc4c(C)cc(Br)cc4OC)n(C)c23)C(C)C)c1 10.1016/j.bmc.2016.08.005
CHEMBL4547748 174191 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 508 7 1 6 7.0 COc1cccc(N(c2cccc3nc(Nc4c(C)cc(Br)cc4OC)n(C)c23)C(C)C)c1 10.1016/j.bmc.2016.08.005
10157505 123855 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 394 5 0 4 5.3 CCCC(C)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL362601 123855 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 394 5 0 4 5.3 CCCC(C)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
58223477 127859 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 482 11 0 9 5.0 CCCN(Cc1ccncc1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664572 127859 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 482 11 0 9 5.0 CCCN(Cc1ccncc1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
58223420 127893 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 486 11 0 9 5.1 COCc1cc(OC)c(-c2csc3c(N(CCCF)c4cccnc4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664605 127893 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 486 11 0 9 5.1 COCc1cc(OC)c(-c2csc3c(N(CCCF)c4cccnc4)c(OC)nn23)c(OC)c1 nan
71580428 88445 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 397 8 1 8 3.1 COc1nc(C)c(Nc2nc(Cl)cn(C(CCF)C3CC3)c2=O)c(OC)n1 10.1016/j.bmcl.2013.02.009
CHEMBL2349572 88445 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 397 8 1 8 3.1 COc1nc(C)c(Nc2nc(Cl)cn(C(CCF)C3CC3)c2=O)c(OC)n1 10.1016/j.bmcl.2013.02.009
137635682 156000 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 480 7 2 6 5.3 CCN(CC(C)O)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4061900 156000 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 480 7 2 6 5.3 CCN(CC(C)O)c1ccc(Br)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
155565844 175617 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 535 7 2 6 6.3 CNC(=O)c1cccc(N(c2cccc3nc(Nc4c(C)cc(Br)cc4OC)n(C)c23)C(C)C)c1 10.1016/j.bmc.2016.08.005
CHEMBL4580457 175617 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 535 7 2 6 6.3 CNC(=O)c1cccc(N(c2cccc3nc(Nc4c(C)cc(Br)cc4OC)n(C)c23)C(C)C)c1 10.1016/j.bmc.2016.08.005
44589203 175957 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 389 4 0 7 4.4 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C)c1 10.1021/jm800743q
CHEMBL458825 175957 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 389 4 0 7 4.4 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C)c1 10.1021/jm800743q
90654667 110072 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 386 9 1 5 6.2 CCCN(CCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)c1SCC 10.1016/j.ejmech.2014.03.040
CHEMBL3235703 110072 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 386 9 1 5 6.2 CCCN(CCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)c1SCC 10.1016/j.ejmech.2014.03.040
10432407 66317 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 422 7 0 4 6.1 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL184938 66317 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 422 7 0 4 6.1 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
10271870 123433 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 392 4 0 4 4.9 CCc1nc2c(n1C(C)C1CC1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL361745 123433 0 None - 0 Rat 7.3 pIC50 = 7.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 392 4 0 4 4.9 CCc1nc2c(n1C(C)C1CC1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
10112643 66352 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 416 6 0 4 6.0 CCc1nc2c(n1C(CC)C(C)C)C(=O)N(C)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049787k
CHEMBL185103 66352 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 416 6 0 4 6.0 CCc1nc2c(n1C(CC)C(C)C)C(=O)N(C)CN2c1ccc(C(C)C)cc1Cl 10.1021/jm049787k
58896411 176205 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-stimulated adenylate cyclase activity measured after 4 hrs by Steady-Glo luciferase assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-stimulated adenylate cyclase activity measured after 4 hrs by Steady-Glo luciferase assay
ChEMBL 464 7 1 6 6.8 COc1ccc(N(c2cccc3nc(Nc4c(C)cc(Cl)cc4OC)n(C)c23)C(C)C)cc1 10.1016/j.bmc.2016.08.005
CHEMBL4593848 176205 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Antagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-stimulated adenylate cyclase activity measured after 4 hrs by Steady-Glo luciferase assayAntagonist activity at human CRF1 receptor expressed in CHO cells assessed as inhibition of CRF-stimulated adenylate cyclase activity measured after 4 hrs by Steady-Glo luciferase assay
ChEMBL 464 7 1 6 6.8 COc1ccc(N(c2cccc3nc(Nc4c(C)cc(Cl)cc4OC)n(C)c23)C(C)C)cc1 10.1016/j.bmc.2016.08.005
58223488 127837 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 473 10 0 9 4.2 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)C4CCOC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664550 127837 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 473 10 0 9 4.2 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)C4CCOC4)c(OC)nn23)c(OC)c1 nan
58223480 127840 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 445 8 0 8 4.8 CCCN(c1c(OC)nn2c(-c3c(OC)cc(C)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664553 127840 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 445 8 0 8 4.8 CCCN(c1c(OC)nn2c(-c3c(OC)cc(C)cc3OC)csc12)C1CCOCC1 nan
11374063 176114 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 440 5 1 6 3.7 COc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C(F)F)c1 10.1021/jm800744m
CHEMBL459173 176114 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 440 5 1 6 3.7 COc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C(F)F)c1 10.1021/jm800744m
44589238 177012 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 409 4 0 7 4.7 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
CHEMBL462789 177012 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 409 4 0 7 4.7 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(Cl)c1 10.1021/jm800743q
70692630 75898 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Anatgonist activity at CRF1 receptor (unknown origin)Anatgonist activity at CRF1 receptor (unknown origin)
ChEMBL 376 7 1 4 6.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.ejmech.2021.114085
CHEMBL2049188 75898 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Anatgonist activity at CRF1 receptor (unknown origin)Anatgonist activity at CRF1 receptor (unknown origin)
ChEMBL 376 7 1 4 6.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)nc12 10.1016/j.ejmech.2021.114085
58223497 127850 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 13 0 9 4.5 COCCCN(CC1CC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664563 127850 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 13 0 9 4.5 COCCCN(CC1CC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
58223377 127854 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 463 13 0 9 4.5 CCCN(CCCOC)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664567 127854 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 463 13 0 9 4.5 CCCN(CCCOC)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
21984746 77548 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 365 8 0 4 5.5 CCCN(CCC)c1c(CC)nn2c(-c3ccc(OC)cc3C)cccc12 10.1021/jm300259r
CHEMBL2087556 77548 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 365 8 0 4 5.5 CCCN(CCC)c1c(CC)nn2c(-c3ccc(OC)cc3C)cccc12 10.1021/jm300259r
24768341 85604 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 378 6 1 6 3.7 CCCCN(CC)c1nc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1C 10.1021/jm0611410
CHEMBL228223 85604 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 378 6 1 6 3.7 CCCCN(CC)c1nc(C)nc2c1NC(=O)CN2c1ccc(C#N)cc1C 10.1021/jm0611410
58223474 127883 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 500 12 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CCCF)Cc4cccnc4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664595 127883 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 500 12 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CCCF)Cc4cccnc4)c(OC)nn23)c(OC)c1 nan
42618210 179811 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 5 0 7 3.3 CCN(CC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL474493 179811 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 367 5 0 7 3.3 CCN(CC)c1nc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm900025h
145969226 164997 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc([C@@H](OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
CHEMBL4225709 164997 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 491 5 0 7 5.5 COc1nc(C)c(N2CCCn3c2nc2c(Cl)ccc([C@@H](OC(F)F)C(F)(F)F)c23)c(C)n1 10.1016/j.bmc.2018.01.020
44589115 175468 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 458 4 0 8 5.0 O=[N+]([O-])c1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
CHEMBL457714 175468 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 458 4 0 8 5.0 O=[N+]([O-])c1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
155520133 173240 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 492 8 1 6 7.6 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3cccc(OC(C)C)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4524490 173240 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 492 8 1 6 7.6 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3cccc(OC(C)C)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
90654668 110073 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 418 11 1 7 4.7 CCSc1c(Nc2c(C)cc(C)cc2C)nc(C)nc1N(CCOC)CCOC 10.1016/j.ejmech.2014.03.040
CHEMBL3235705 110073 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysisDisplacement of [125I]Tyr0sauvagine from human CRF1 receptor expressed in HEK293 cell membrane after 120 mins by gamma scintillation counting analysis
ChEMBL 418 11 1 7 4.7 CCSc1c(Nc2c(C)cc(C)cc2C)nc(C)nc1N(CCOC)CCOC 10.1016/j.ejmech.2014.03.040
58223491 127864 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 13 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CCOC(C)C)CC4CC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664577 127864 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 13 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CCOC(C)C)CC4CC4)c(OC)nn23)c(OC)c1 nan
22177860 64745 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 432 6 1 5 5.8 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C(F)(F)F)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819069 64745 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 432 6 1 5 5.8 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C(F)(F)F)nn13)CCC2 10.1016/j.bmc.2011.07.055
67364197 130603 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 519 5 1 5 6.2 Cc1cc(-c2ccc3c(c2)OCO3)nn1C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3681386 130603 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 519 5 1 5 6.2 Cc1cc(-c2ccc3c(c2)OCO3)nn1C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
56678852 64759 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 372 6 1 5 5.3 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3Cl)c(C)nn12 10.1016/j.bmc.2011.07.055
CHEMBL1819084 64759 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 372 6 1 5 5.3 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3Cl)c(C)nn12 10.1016/j.bmc.2011.07.055
10112776 166214 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 418 5 0 4 5.3 CCc1nc2c(n1C(C1CC1)C1CC1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL426607 166214 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 418 5 0 4 5.3 CCc1nc2c(n1C(C1CC1)C1CC1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
42618201 179251 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 447 7 1 7 4.8 CCC(CC)Nc1nc(C)nc2c(-c3cc(OC)c(OC)cc3Br)c(C)nn12 10.1021/jm9000242
CHEMBL472873 179251 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 447 7 1 7 4.8 CCC(CC)Nc1nc(C)nc2c(-c3cc(OC)c(OC)cc3Br)c(C)nn12 10.1021/jm9000242
42618167 180653 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 339 5 0 6 3.6 CCN(CC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL475505 180653 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 339 5 0 6 3.6 CCN(CC)c1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
10379 3059 39 None - 1 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at human CRF1 receptorAntagonist activity at human CRF1 receptor
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1124/dmd.111.043596
9884366 3059 39 None - 1 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at human CRF1 receptorAntagonist activity at human CRF1 receptor
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1124/dmd.111.043596
CHEMBL482950 3059 39 None - 1 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at human CRF1 receptorAntagonist activity at human CRF1 receptor
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1124/dmd.111.043596
DB12572 3059 39 None - 1 Human 8.2 pIC50 = 8.2 Binding
Antagonist activity at human CRF1 receptorAntagonist activity at human CRF1 receptor
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1124/dmd.111.043596
11552261 65510 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 361 5 1 5 5.7 CCC(CC)n1ccc2c(Nc3c(C)cc(C)cc3C)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
CHEMBL1830527 65510 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 361 5 1 5 5.7 CCC(CC)n1ccc2c(Nc3c(C)cc(C)cc3C)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
10379 3059 39 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm200365y
9884366 3059 39 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm200365y
CHEMBL482950 3059 39 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm200365y
DB12572 3059 39 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm200365y
10379 3059 39 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
9884366 3059 39 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
CHEMBL482950 3059 39 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
DB12572 3059 39 None - 1 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 10.1021/jm900025h
46891032 6669 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 398 7 1 7 3.6 COCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1083420 6669 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 398 7 1 7 3.6 COCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
46891091 6822 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 434 8 1 7 4.2 COCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1083948 6822 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 434 8 1 7 4.2 COCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
46891034 7402 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 420 5 1 5 5.4 CCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1086509 7402 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 420 5 1 5 5.4 CCC(C1CC1)n1nc(C)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
44190240 196740 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 382 4 1 5 4.8 C[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900301y
CHEMBL565144 196740 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 382 4 1 5 4.8 C[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C#N)cc2Cl)c1=O 10.1021/jm900301y
24768327 98037 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 392 7 2 6 4.4 CC[C@@H](CO)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C(=O)OC 10.1021/jm070579c
CHEMBL273040 98037 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 392 7 2 6 4.4 CC[C@@H](CO)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C(=O)OC 10.1021/jm070579c
24768327 98037 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 392 7 2 6 4.4 CC[C@@H](CO)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C(=O)OC 10.1021/jm070579c
CHEMBL273040 98037 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 392 7 2 6 4.4 CC[C@@H](CO)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C(=O)OC 10.1021/jm070579c
42618185 179816 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 369 6 0 7 3.6 CCCN(C)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL474499 179816 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 369 6 0 7 3.6 CCCN(C)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
52918269 61041 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 397 8 0 8 3.2 COc1ccc(-c2c(C)nn3c(N(CCC#N)CCCF)nc(C)nc23)c(C)n1 10.1016/j.bmcl.2011.02.050
CHEMBL1762822 61041 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 397 8 0 8 3.2 COc1ccc(-c2c(C)nn3c(N(CCC#N)CCCF)nc(C)nc23)c(C)n1 10.1016/j.bmcl.2011.02.050
46891289 6883 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 343 6 1 7 3.1 CCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1084205 6883 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 343 6 1 7 3.1 CCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(OC)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
46891553 7343 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 395 8 1 8 2.9 COC[C@H](C1CC1)n1nc(C)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1086240 7343 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 395 8 1 8 2.9 COC[C@H](C1CC1)n1nc(C)nc(Nc2cc(C)c(OC(F)F)nc2C)c1=O 10.1016/j.bmcl.2010.04.121
44191014 195026 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 441 5 1 5 5.8 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL549320 195026 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 441 5 1 5 5.8 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(OC(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
44190335 196075 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 331 5 1 4 4.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2ccc(C)cc2C)c1=O 10.1021/jm900301y
CHEMBL560633 196075 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 331 5 1 4 4.6 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2ccc(C)cc2C)c1=O 10.1021/jm900301y
42618228 180659 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 370 7 0 8 2.6 CCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL475507 180659 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 370 7 0 8 2.6 CCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
46891230 6393 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 369 5 1 7 3.1 COc1ccc(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1082300 6393 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 369 5 1 7 3.1 COc1ccc(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
127047692 139857 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 441 8 1 8 4.1 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3cccnc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3799211 139857 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 441 8 1 8 4.1 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3cccnc3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
44190557 196532 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 379 5 1 7 3.3 COc1ccc(Nc2nc(C#N)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
CHEMBL563652 196532 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 379 5 1 7 3.3 COc1ccc(Nc2nc(C#N)cn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1021/jm900301y
10377 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
9818802 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
CHEMBL270738 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
10377 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
9818802 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
CHEMBL270738 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
10377 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm200365y
9818802 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm200365y
CHEMBL270738 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm200365y
127047549 139962 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 466 8 1 9 4.0 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3cc(C#N)ccn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3799801 139962 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 466 8 1 9 4.0 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3cc(C#N)ccn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
46881790 7266 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 387 5 1 6 4.2 Cc1cc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)nc1N1CCCC1 10.1016/j.bmcl.2010.01.129
CHEMBL1085930 7266 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 387 5 1 6 4.2 Cc1cc(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)nc1N1CCCC1 10.1016/j.bmcl.2010.01.129
10377 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
9818802 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
CHEMBL270738 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070579c
10377 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
9818802 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
CHEMBL270738 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
10377 1179 27 None -1 2 Human 8.2 pIC50 = 8.2 Binding
Inhibition of CRF1 receptorInhibition of CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
9818802 1179 27 None -1 2 Human 8.2 pIC50 = 8.2 Binding
Inhibition of CRF1 receptorInhibition of CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
CHEMBL270738 1179 27 None -1 2 Human 8.2 pIC50 = 8.2 Binding
Inhibition of CRF1 receptorInhibition of CRF1 receptor
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1021/jm070578k
24768333 85584 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 400 8 1 8 2.9 CCCCN(CC)c1nc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1OC 10.1021/jm0611410
CHEMBL228169 85584 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 400 8 1 8 2.9 CCCCN(CC)c1nc(C)nc2c1NC(=O)CN2c1ccc(OC)nc1OC 10.1021/jm0611410
46891157 6493 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 323 4 1 6 3.2 Cc1nc(Nc2cc(C)c(C#N)cc2C)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1082705 6493 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 323 4 1 6 3.2 Cc1nc(Nc2cc(C)c(C#N)cc2C)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
44589305 188703 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 390 4 0 8 3.8 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C)n1 10.1021/jm800743q
CHEMBL504383 188703 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 390 4 0 8 3.8 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C)n1 10.1021/jm800743q
10294046 64754 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 394 7 1 6 4.8 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)c(OC)c4)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819079 64754 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 394 7 1 6 4.8 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)c(OC)c4)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
58223382 82600 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 519 11 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4(F)CCOCC4)c(OC)nn23)c(OC)c1 nan
CHEMBL2179178 82600 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 519 11 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4(F)CCOCC4)c(OC)nn23)c(OC)c1 nan
58223515 127875 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 12 0 9 5.0 COCCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCC1 nan
CHEMBL3664588 127875 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 12 0 9 5.0 COCCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCCC1 nan
58223449 127876 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 457 8 0 8 5.0 CCN(c1c(OC)nn2c(-c3c(OC)cc(C4CC4)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664589 127876 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 457 8 0 8 5.0 CCN(c1c(OC)nn2c(-c3c(OC)cc(C4CC4)cc3OC)csc12)C1CCOCC1 nan
58223517 127882 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 500 12 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CCCF)Cc4ccncc4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664594 127882 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 500 12 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CCCF)Cc4ccncc4)c(OC)nn23)c(OC)c1 nan
56673724 65301 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 373 8 1 6 4.8 CCCN(CCC)c1cc(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828888 65301 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 373 8 1 6 4.8 CCCN(CCC)c1cc(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
58223382 82600 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 519 11 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4(F)CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179178 82600 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 519 11 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4(F)CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
21912450 98012 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 1 4 5.2 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(CO)cc2C)c1C 10.1021/jm070578k
CHEMBL272904 98012 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 1 4 5.2 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(CO)cc2C)c1C 10.1021/jm070578k
21912450 98012 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 1 4 5.2 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(CO)cc2C)c1C 10.1021/jm070578k
CHEMBL272904 98012 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 343 7 1 4 5.2 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(CO)cc2C)c1C 10.1021/jm070578k
58223461 127896 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 499 11 0 9 4.3 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4C5COCC54)c(OC)nn23)c(OC)c1 nan
CHEMBL3664608 127896 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 499 11 0 9 4.3 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4C5COCC54)c(OC)nn23)c(OC)c1 nan
71455050 81512 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(Cl)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160161 81512 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(Cl)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
22177936 64746 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 424 8 1 6 5.7 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(CSC)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819070 64746 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 424 8 1 6 5.7 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(CSC)nn13)CCC2 10.1016/j.bmc.2011.07.055
10495051 187176 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 308 3 1 4 4.4 CCNc1nc(C)nc2c1c(C)cn2-c1c(C)cc(C)cc1C 10.1021/jm960861b
CHEMBL49217 187176 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 308 3 1 4 4.4 CCNc1nc(C)nc2c1c(C)cn2-c1c(C)cc(C)cc1C 10.1021/jm960861b
10161139 65197 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 450 8 0 4 6.9 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)C(CC)N2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL182497 65197 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 450 8 0 4 6.9 CCCC(CCC)n1c(CC)nc2c1C(=O)N(C)C(CC)N2c1ccc(Cl)cc1Cl 10.1021/jm049787k
58223442 127889 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 12 0 9 5.4 CCCCN(c1c(OCC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664601 127889 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 12 0 9 5.4 CCCCN(c1c(OCC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 nan
44478733 82615 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 479 9 0 8 5.3 CCCN(c1c(OC)nn2c(-c3c(Cl)cc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179193 82615 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 479 9 0 8 5.3 CCCN(c1c(OC)nn2c(-c3c(Cl)cc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
44191106 196358 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 435 5 1 6 4.3 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(S(C)(=O)=O)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL562492 196358 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 435 5 1 6 4.3 C[C@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(S(C)(=O)=O)cc2Cl)c1=O 10.1021/jm900302q
44444335 94466 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 349 5 0 4 5.4 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)cc1)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL251344 94466 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 349 5 0 4 5.4 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC)cc1)CC2 10.1016/j.bmcl.2007.06.077
53358379 130601 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 394 4 1 4 4.2 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)cnc3C)CC2)n1 nan
CHEMBL3681384 130601 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 394 4 1 4 4.2 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(C(F)(F)F)cnc3C)CC2)n1 nan
58223511 127842 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 459 9 0 8 5.0 CCCN(c1c(OC)nn2c(-c3c(OC)cc(CC)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664555 127842 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 459 9 0 8 5.0 CCCN(c1c(OC)nn2c(-c3c(OC)cc(CC)cc3OC)csc12)C1CCOCC1 nan
70681899 75585 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 480 10 0 7 5.8 CCN(CC1CCOCC1)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2046528 75585 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 480 10 0 7 5.8 CCN(CC1CCOCC1)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
11271502 139406 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 476 10 1 7 4.5 COCCN(CCOC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793560 139406 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 476 10 1 7 4.5 COCCN(CCOC)c1cccc2nc(Nc3c(C)cc(Br)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
71457262 82613 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 489 11 0 9 5.0 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179191 82613 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 489 11 0 9 5.0 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
46881745 7221 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 332 4 1 5 3.9 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)n1 10.1016/j.bmcl.2010.01.129
CHEMBL1085683 7221 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 332 4 1 5 3.9 Cc1cc(C)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)c(C)n1 10.1016/j.bmcl.2010.01.129
58223516 127885 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 493 11 0 8 5.7 COCCCN(c1c(OC)nn2c(-c3c(Cl)cc(COC)cc3OC)csc12)C1CCCC1 nan
CHEMBL3664597 127885 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 493 11 0 8 5.7 COCCCN(c1c(OC)nn2c(-c3c(Cl)cc(COC)cc3OC)csc12)C1CCCC1 nan
57786313 164984 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 418 3 0 4 6.6 CCC(C#N)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4225575 164984 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 418 3 0 4 6.6 CCC(C#N)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
11223423 189542 30 None - 1 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 404 4 1 6 3.1 COc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL514270 189542 30 None - 1 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 404 4 1 6 3.1 COc1ccc(N2CCc3c(-n4ccc(N5CCNC5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
53358376 130605 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 376 5 2 5 3.0 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(CO)cc2C)CC1 nan
CHEMBL3681388 130605 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 376 5 2 5 3.0 Cc1ncc(Cl)cc1C(=O)N[C@H]1CC[C@H](Cn2nc(CO)cc2C)CC1 nan
56683764 65503 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 387 8 0 6 4.8 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
CHEMBL1830520 65503 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 387 8 0 6 4.8 CCCN(CCC)c1cc(N(C)c2ccc(OC)cc2Cl)nc2nccn12 10.1016/j.bmc.2011.08.055
71449705 81508 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(OC)c2nc(-c3c(Cl)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160157 81508 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(OC)c2nc(-c3c(Cl)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
127047520 140068 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 469 8 1 9 3.9 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)c3ccccn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3800457 140068 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 469 8 1 9 3.9 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COC(=O)c3ccccn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
3520 3267 54 None 1 2 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmc.2016.11.011
9821250 3267 54 None 1 2 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmc.2016.11.011
CHEMBL309138 3267 54 None 1 2 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes preincubated for 1 hr followed by compound washout for 2 hrs and subsequent addition of [125I]-CRF measured after 1 hr by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmc.2016.11.011
53357658 130608 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 429 5 1 4 4.9 COc1cc(C)nn1C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
CHEMBL3681391 130608 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 429 5 1 4 4.9 COc1cc(C)nn1C[C@H]1CC[C@H](NC(=O)c2cc(C(F)(F)F)ccc2Cl)CC1 nan
11317069 174981 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 458 4 1 6 4.0 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(OC(F)(F)F)cc1C)CC2 10.1021/jm800744m
CHEMBL456640 174981 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 458 4 1 6 4.0 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(OC(F)(F)F)cc1C)CC2 10.1021/jm800744m
11350078 189787 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 399 3 1 6 3.0 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(C#N)cc1C)CC2 10.1021/jm800744m
CHEMBL516170 189787 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 399 3 1 6 3.0 Cc1cc(-n2ccc(N3CCNC3=O)n2)c2c(n1)N(c1ccc(C#N)cc1C)CC2 10.1021/jm800744m
70692632 75901 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 392 7 1 5 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)n(C)c12 10.1016/j.bmcl.2012.05.066
CHEMBL2049191 75901 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 392 7 1 5 5.2 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(=O)n(C)c12 10.1016/j.bmcl.2012.05.066
46890980 6840 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 328 5 1 6 3.3 COc1cc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C)c1 10.1016/j.bmcl.2010.04.121
CHEMBL1084026 6840 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 328 5 1 6 3.3 COc1cc(C)c(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C)c1 10.1016/j.bmcl.2010.04.121
44397042 12270 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 408 6 2 5 4.6 CCC(CNc1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl)OC 10.1021/jm049737f
CHEMBL1184732 12270 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 408 6 2 5 4.6 CCC(CNc1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl)OC 10.1021/jm049737f
CHEMBL365868 12270 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 408 6 2 5 4.6 CCC(CNc1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl)OC 10.1021/jm049737f
56683761 65495 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 431 11 0 7 4.8 CCCN(CCC)c1cc(N(CCOC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830513 65495 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 431 11 0 7 4.8 CCCN(CCC)c1cc(N(CCOC)c2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
71451919 82598 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 501 11 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CC4CCOCC4)CC4CC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179176 82598 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 501 11 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CC4CCOCC4)CC4CC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
46891389 6486 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 398 7 1 7 3.6 COC[C@@H](C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1082671 6486 0 None - 0 Rat 7.2 pIC50 = 7.2 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 398 7 1 7 3.6 COC[C@@H](C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
58896587 173369 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 449 6 1 6 6.5 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3ccc(C)cn3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4527586 173369 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 449 6 1 6 6.5 COc1cc(Cl)cc(C)c1Nc1nc2cccc(N(c3ccc(C)cn3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
155548925 173815 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 503 6 1 6 6.8 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(C#N)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4538409 173815 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 503 6 1 6 6.8 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(C#N)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
53358268 130604 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 376 5 2 5 3.0 Cc1cc(CO)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
CHEMBL3681387 130604 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 376 5 2 5 3.0 Cc1cc(CO)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
11703582 65511 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 378 7 0 6 5.4 CCc1ccc(Oc2nc3ccnn3c3c2ccn3C(CC)CC)c(OC)c1 10.1016/j.bmc.2011.08.055
CHEMBL1830528 65511 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 378 7 0 6 5.4 CCc1ccc(Oc2nc3ccnn3c3c2ccn3C(CC)CC)c(OC)c1 10.1016/j.bmc.2011.08.055
10376 2930 4 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from corticotropin-releasing factor receptor 1 in rat brain membranes after 2 hrs by gamma countingDisplacement of [125I]CRF from corticotropin-releasing factor receptor 1 in rat brain membranes after 2 hrs by gamma counting
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
9801039 2930 4 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from corticotropin-releasing factor receptor 1 in rat brain membranes after 2 hrs by gamma countingDisplacement of [125I]CRF from corticotropin-releasing factor receptor 1 in rat brain membranes after 2 hrs by gamma counting
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
CHEMBL1819077 2930 4 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from corticotropin-releasing factor receptor 1 in rat brain membranes after 2 hrs by gamma countingDisplacement of [125I]CRF from corticotropin-releasing factor receptor 1 in rat brain membranes after 2 hrs by gamma counting
ChEMBL 398 6 1 5 5.5 CCC(Nc1c2CCCc2nc2n1nc(c2c1ccc(cc1Cl)OC)C)CC 10.1016/j.bmc.2011.07.055
56668633 64761 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 400 6 1 6 4.9 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)CCO2 10.1016/j.bmc.2011.07.055
CHEMBL1819086 64761 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 400 6 1 6 4.9 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)CCO2 10.1016/j.bmc.2011.07.055
42618221 179632 11 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 1 7 3.3 CC[C@H](C)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL474288 179632 11 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 340 5 1 7 3.3 CC[C@H](C)Nc1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
56670271 65509 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 360 5 0 4 5.6 CCC(CC)n1ccc2c(Cc3c(C)cc(C)cc3C)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
CHEMBL1830526 65509 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 360 5 0 4 5.6 CCC(CC)n1ccc2c(Cc3c(C)cc(C)cc3C)nc3ccnn3c21 10.1016/j.bmc.2011.08.055
57786006 164963 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 422 4 0 4 6.4 CCN(CC)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4225254 164963 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 422 4 0 4 6.4 CCN(CC)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
11407418 66721 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 416 6 1 4 4.9 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccccc1Br 10.1021/jm049737f
CHEMBL185648 66721 0 None - 0 Rat 8.2 pIC50 = 8.2 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 416 6 1 4 4.9 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccccc1Br 10.1021/jm049737f
46891492 6564 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 398 7 1 7 3.6 COC[C@H](C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1083011 6564 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 398 7 1 7 3.6 COC[C@H](C1CC1)n1nc(C)nc(Nc2c(Cl)cc(OC)cc2Cl)c1=O 10.1016/j.bmcl.2010.04.121
46891441 7068 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 404 6 1 6 4.6 Cc1nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c(=O)n([C@@H](C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1084988 7068 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 404 6 1 6 4.6 Cc1nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c(=O)n([C@@H](C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
10405373 97403 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 346 6 1 3 6.4 CCC(CC)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C 10.1021/jm070579c
CHEMBL269833 97403 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 346 6 1 3 6.4 CCC(CC)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C 10.1021/jm070579c
10405373 97403 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 346 6 1 3 6.4 CCC(CC)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C 10.1021/jm070579c
CHEMBL269833 97403 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 346 6 1 3 6.4 CCC(CC)Nc1cc(C)nc(Oc2c(C)cc(Cl)cc2C)c1C 10.1021/jm070579c
54754515 65300 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 373 7 2 6 5.0 CCC(CC)Nc1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828887 65300 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 373 7 2 6 5.0 CCC(CC)Nc1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
71580314 88439 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 404 8 1 6 4.1 Cc1cc(C#N)cc(C)c1Nc1nc(Cl)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
CHEMBL2349565 88439 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 404 8 1 6 4.1 Cc1cc(C#N)cc(C)c1Nc1nc(Cl)cn([C@@H](COCCF)C2CC2)c1=O 10.1016/j.bmcl.2013.02.009
24758075 69982 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 350 5 0 4 5.3 CCC(CC)c1cc(C)n2nc(-c3cnc(N(C)C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
CHEMBL1939577 69982 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 350 5 0 4 5.3 CCC(CC)c1cc(C)n2nc(-c3cnc(N(C)C)cc3C)c(C)cc12 10.1016/j.bmc.2011.11.015
58012370 158160 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 433 8 1 4 7.6 CCCC(CCC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4087369 158160 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 433 8 1 4 7.6 CCCC(CCC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
46891440 6397 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 368 5 1 6 4.0 COc1cc(Cl)c(Nc2nc(C)nn([C@@H](C)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2010.04.121
CHEMBL1082309 6397 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 368 5 1 6 4.0 COc1cc(Cl)c(Nc2nc(C)nn([C@@H](C)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2010.04.121
44191185 195935 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 416 4 1 5 5.2 C[C@H](C1CC1)n1cc(C#N)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL559443 195935 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 416 4 1 5 5.2 C[C@H](C1CC1)n1cc(C#N)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
127030925 139493 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 386 6 1 5 5.4 CCN(CC)c1ccc(C)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794475 139493 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 386 6 1 5 5.4 CCN(CC)c1ccc(C)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
10713700 101910 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 362 5 0 4 5.4 C/C=C/CN(CC)c1nc(C)nc2c1c(C)cn2-c1c(C)cc(C)cc1C 10.1021/jm960861b
CHEMBL300935 101910 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneInhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membrane
ChEMBL 362 5 0 4 5.4 C/C=C/CN(CC)c1nc(C)nc2c1c(C)cn2-c1c(C)cc(C)cc1C 10.1021/jm960861b
71580216 88435 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 440 9 1 7 4.1 COc1cc(Cl)c(Nc2nc(C#N)cn([C@@H](COCCF)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2013.02.009
CHEMBL2349561 88435 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma countingDisplacement of [125I]-o-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting
ChEMBL 440 9 1 7 4.1 COc1cc(Cl)c(Nc2nc(C#N)cn([C@@H](COCCF)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2013.02.009
127047691 139680 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 466 8 1 9 4.0 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3ccc(C#N)cn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3797955 139680 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 466 8 1 9 4.0 COc1nc(C)c(Nc2nc(Cl)cn([C@H](COc3ccc(C#N)cn3)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
56961967 81995 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 425 8 1 7 3.2 COCC(COC)n1cc(Br)nc(Nc2c(C)cc(OC)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
CHEMBL2165200 81995 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counterDisplacement of [125I]-o-CRF from CRFR1 in rat frontal cortex after 2 hrs by gamma counter
ChEMBL 425 8 1 7 3.2 COCC(COC)n1cc(Br)nc(Nc2c(C)cc(OC)cc2C)c1=O 10.1016/j.bmcl.2012.08.112
57400679 69989 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 383 7 1 6 3.7 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CCO)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939584 69989 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 383 7 1 6 3.7 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CCO)c(=O)c12 10.1016/j.bmc.2011.11.015
57393714 70003 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 367 5 0 6 3.7 CCC(CC)c1cc(C)n2nc(-c3ccc(N(C)C)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939598 70003 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 367 5 0 6 3.7 CCC(CC)c1cc(C)n2nc(-c3ccc(N(C)C)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
44191105 195248 1 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 425 4 1 4 5.9 C[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL551029 195248 1 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 425 4 1 4 5.9 C[C@@H](C1CC1)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
58012303 156791 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 409 5 1 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4070898 156791 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 409 5 1 3 7.5 CCC(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
42618190 179279 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 429 10 0 9 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
CHEMBL473076 179279 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 429 10 0 9 2.8 COCCN(CCOC)c1nc(C)nc2c(-c3c(C)cc(OC)cc3OC)c(C)nn12 10.1021/jm9000242
60141295 75588 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 410 9 0 6 5.3 CCN(CC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2046534 75588 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 410 9 0 6 5.3 CCN(CC)c1cccc2nc(Oc3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.05.066
57912459 82617 5 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 503 12 0 9 5.4 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179195 82617 5 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 503 12 0 9 5.4 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(COCC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
58223389 127836 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 505 12 0 10 4.5 CCCCN(CC1COCOC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664549 127836 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 505 12 0 10 4.5 CCCCN(CC1COCOC1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
22178019 64755 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 412 7 1 5 5.8 CCOc1ccc(-c2c(C)nn3c(NC(CC)CC)c4c(nc23)CCC4)c(Cl)c1 10.1016/j.bmc.2011.07.055
CHEMBL1819080 64755 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 412 7 1 5 5.8 CCOc1ccc(-c2c(C)nn3c(NC(CC)CC)c4c(nc23)CCC4)c(Cl)c1 10.1016/j.bmc.2011.07.055
24768345 85530 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 395 7 1 6 4.0 CCCCN(CC)c1nc(C)nc2c1NC(=O)CN2c1ccc(C(C)=O)cc1C 10.1021/jm0611410
CHEMBL227572 85530 0 None - 0 Rat 6.2 pIC50 = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 395 7 1 6 4.0 CCCCN(CC)c1nc(C)nc2c1NC(=O)CN2c1ccc(C(C)=O)cc1C 10.1021/jm0611410
22177924 64747 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 362 5 1 4 5.4 CCC(CC)Nc1c2c(nc3c(-c4ccc(C)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819071 64747 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 362 5 1 4 5.4 CCC(CC)Nc1c2c(nc3c(-c4ccc(C)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
46881791 7267 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 372 4 1 5 4.3 Cc1nc(C(F)(F)F)ccc1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1085931 7267 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 372 4 1 5 4.3 Cc1nc(C(F)(F)F)ccc1Nc1nc(Cl)cn([C@H](C)C2CC2)c1=O 10.1016/j.bmcl.2010.01.129
58223439 127874 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 12 0 9 4.6 COCCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCC1 nan
CHEMBL3664587 127874 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 475 12 0 9 4.6 COCCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCC1 nan
58223408 127849 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 465 8 0 8 5.1 CCCN(c1c(OC)nn2c(-c3c(OC)cc(Cl)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664562 127849 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 465 8 0 8 5.1 CCCN(c1c(OC)nn2c(-c3c(OC)cc(Cl)cc3OC)csc12)C1CCOCC1 nan
58223434 128814 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 517 12 0 9 5.8 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(COC(C)C)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3669432 128814 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 517 12 0 9 5.8 CCCCN(c1c(OC)nn2c(-c3c(OC)cc(COC(C)C)cc3OC)csc12)C1CCOCC1 nan
46881746 6924 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 346 4 1 6 3.3 Cc1nc2c(cc1Nc1nc(Cl)cn([C@H](C)C3CC3)c1=O)COC2 10.1016/j.bmcl.2010.01.129
CHEMBL1084422 6924 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 346 4 1 6 3.3 Cc1nc2c(cc1Nc1nc(Cl)cn([C@H](C)C3CC3)c1=O)COC2 10.1016/j.bmcl.2010.01.129
21912204 97705 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 325 6 2 3 6.0 CCC(CC)Nc1cc(C)nc(Nc2c(C)cc(C)cc2C)c1C 10.1021/jm070579c
CHEMBL271368 97705 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 325 6 2 3 6.0 CCC(CC)Nc1cc(C)nc(Nc2c(C)cc(C)cc2C)c1C 10.1021/jm070579c
44589258 175678 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 395 3 0 8 3.8 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C#N)c1 10.1021/jm800743q
CHEMBL458177 175678 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 395 3 0 8 3.8 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C#N)c1 10.1021/jm800743q
70690480 75904 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 443 7 1 4 6.9 Cc1cc(C)c(Nc2nc3cccc(N(CC4CCOCC4)CC4CC4)c3cc2C)c(C)c1 10.1016/j.bmcl.2012.05.066
CHEMBL2049195 75904 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 443 7 1 4 6.9 Cc1cc(C)c(Nc2nc3cccc(N(CC4CCOCC4)CC4CC4)c3cc2C)c(C)c1 10.1016/j.bmcl.2012.05.066
58223505 127884 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 500 12 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CCCF)Cc4ccccn4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664596 127884 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 500 12 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CCCF)Cc4ccccn4)c(OC)nn23)c(OC)c1 nan
70688433 75903 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 399 7 1 3 6.8 Cc1cc(C)c(Nc2nc3cccc(N(CC4CC4)CC4CC4)c3cc2C)c(C)c1 10.1016/j.bmcl.2012.05.066
CHEMBL2049194 75903 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 399 7 1 3 6.8 Cc1cc(C)c(Nc2nc3cccc(N(CC4CC4)CC4CC4)c3cc2C)c(C)c1 10.1016/j.bmcl.2012.05.066
71450106 82602 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 501 11 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCCCO4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179180 82602 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 501 11 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4CCCCO4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
155541854 173045 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 549 7 1 6 6.6 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(C(=O)N(C)C)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4519158 173045 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 549 7 1 6 6.6 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(C(=O)N(C)C)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
10127304 65249 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 436 7 0 6 4.9 CCCC(CCC)n1c(CC)nc2c1c(=O)n(C)c(=O)n2-c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL182744 65249 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 436 7 0 6 4.9 CCCC(CCC)n1c(CC)nc2c1c(=O)n(C)c(=O)n2-c1ccc(Cl)cc1Cl 10.1021/jm049787k
9843355 11230 2 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using HEK293 cells expressing h-CRF1 receptorInhibition of corticotropin releasing factor receptor mediated increase in cAMP level using HEK293 cells expressing h-CRF1 receptor
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
CHEMBL1178813 11230 2 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using HEK293 cells expressing h-CRF1 receptorInhibition of corticotropin releasing factor receptor mediated increase in cAMP level using HEK293 cells expressing h-CRF1 receptor
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
CHEMBL44169 11230 2 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using HEK293 cells expressing h-CRF1 receptorInhibition of corticotropin releasing factor receptor mediated increase in cAMP level using HEK293 cells expressing h-CRF1 receptor
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
21912204 97705 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 325 6 2 3 6.0 CCC(CC)Nc1cc(C)nc(Nc2c(C)cc(C)cc2C)c1C 10.1021/jm070579c
CHEMBL271368 97705 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Displacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counterDisplacement of [125I]oCRF from rat CRF1 after 2 hrs by Betaplate scintillation counter
ChEMBL 325 6 2 3 6.0 CCC(CC)Nc1cc(C)nc(Nc2c(C)cc(C)cc2C)c1C 10.1021/jm070579c
58223421 82486 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 499 10 0 8 5.5 COCc1cc(OC)c(-c2c(C)sc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 nan
CHEMBL2177105 82486 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 499 10 0 8 5.5 COCc1cc(OC)c(-c2c(C)sc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 nan
58223447 127887 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 11 0 9 5.3 CCCN(c1c(OCC)nn2c(-c3c(OC)cc(OCC)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664599 127887 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 11 0 9 5.3 CCCN(c1c(OCC)nn2c(-c3c(OC)cc(OCC)cc3OC)csc12)C1CCOCC1 nan
58223421 82486 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 499 10 0 8 5.5 COCc1cc(OC)c(-c2c(C)sc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2177105 82486 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 499 10 0 8 5.5 COCc1cc(OC)c(-c2c(C)sc3c(N(CC4CCOCC4)CC4CC4)c(C)nn23)c(OC)c1 10.1021/jm300864p
44190056 196345 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 363 7 1 5 4.7 CCC(CC)Cn1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
CHEMBL562435 196345 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 363 7 1 5 4.7 CCC(CC)Cn1cc(Cl)nc(Nc2cc(C)c(OC)cc2C)c1=O 10.1021/jm900301y
9865624 15544 12 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1021/jm040058e
CHEMBL121896 15544 12 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1021/jm040058e
56663337 65313 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 427 10 0 6 5.7 C=C(C)CN(c1cc(N(CCC)CCC)n2nccc2n1)c1ccc(OC)cc1Cl 10.1016/j.bmc.2011.08.055
CHEMBL1828899 65313 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 427 10 0 6 5.7 C=C(C)CN(c1cc(N(CCC)CCC)n2nccc2n1)c1ccc(OC)cc1Cl 10.1016/j.bmc.2011.08.055
70690301 75584 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 506 11 0 7 6.1 COCc1cc(OC)c(Oc2nc3cccc(N(CC4CCOCC4)CC4CC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.05.066
CHEMBL2046527 75584 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 506 11 0 7 6.1 COCc1cc(OC)c(Oc2nc3cccc(N(CC4CCOCC4)CC4CC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.05.066
58223384 127880 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 11 0 9 5.4 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC(C)C)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3664592 127880 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 11 0 9 5.4 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC(C)C)cc3OC)csc12)C1CCOCC1 nan
58896519 139384 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 367 7 1 4 6.6 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)sc12 10.1021/acs.jmedchem.5b01715
CHEMBL3793190 139384 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 367 7 1 4 6.6 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)sc12 10.1021/acs.jmedchem.5b01715
54582017 60648 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 352 4 0 5 3.7 CCN(CC)c1nc2c(c(-c3c(C)cc(C)cc3C)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760252 60648 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 352 4 0 5 3.7 CCN(CC)c1nc2c(c(-c3c(C)cc(C)cc3C)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
70686532 76611 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 408 8 0 5 5.5 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063372 76611 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 408 8 0 5 5.5 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
70692469 75582 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 376 7 0 3 6.9 CCCN(CCC)c1cccc2nc(Oc3c(C)cc(C)cc3C)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2046525 75582 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 376 7 0 3 6.9 CCCN(CCC)c1cccc2nc(Oc3c(C)cc(C)cc3C)c(C)cc12 10.1016/j.bmcl.2012.05.066
9843355 11230 2 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using rat cortical homogenates in vitro.Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using rat cortical homogenates in vitro.
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
CHEMBL1178813 11230 2 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using rat cortical homogenates in vitro.Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using rat cortical homogenates in vitro.
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
CHEMBL44169 11230 2 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using rat cortical homogenates in vitro.Inhibition of corticotropin releasing factor receptor mediated increase in cAMP level using rat cortical homogenates in vitro.
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
44444325 94326 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 417 5 0 4 6.6 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC(F)(F)F)cc1C)CC2 10.1016/j.bmcl.2007.06.077
CHEMBL250603 94326 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membraneDisplacement of [125I]CRF from human recombinant CRF1 receptor expressed in CHO cell membrane
ChEMBL 417 5 0 4 6.6 CCC(CC)n1cc2c3c(nc(C)cc31)N(c1ccc(OC(F)(F)F)cc1C)CC2 10.1016/j.bmcl.2007.06.077
11200917 189708 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 418 4 0 6 3.5 COc1ccc(N2CCc3c(-n4ccc(N5CCN(C)C5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
CHEMBL515532 189708 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 418 4 0 6 3.5 COc1ccc(N2CCc3c(-n4ccc(N5CCN(C)C5=O)n4)cc(C)nc32)c(C)c1 10.1021/jm800744m
11383650 65302 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
CHEMBL1828889 65302 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 387 8 1 6 5.1 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ccnn12 10.1016/j.bmc.2011.08.055
56659948 65499 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 388 8 1 7 4.5 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
CHEMBL1830517 65499 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 388 8 1 7 4.5 CCCN(CCC)c1c(C)c(Nc2ccc(OC)cc2Cl)nc2ncnn12 10.1016/j.bmc.2011.08.055
42618200 184165 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 449 10 0 9 3.2 COCCN(CCOC)c1nc(C)nc2c(-c3cc(OC)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
CHEMBL482983 184165 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 449 10 0 9 3.2 COCCN(CCOC)c1nc(C)nc2c(-c3cc(OC)c(OC)cc3Cl)c(C)nn12 10.1021/jm9000242
42618233 184215 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 0 7 3.4 CCCCN(C)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL483350 184215 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 354 6 0 7 3.4 CCCCN(C)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
24768344 85542 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 380 7 1 5 5.1 CCCCN(CC)c1cc(C)nc2c1NCCN2c1ccc(C(C)=O)cc1C 10.1021/jm0611410
CHEMBL227731 85542 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 380 7 1 5 5.1 CCCCN(CC)c1cc(C)nc2c1NCCN2c1ccc(C(C)=O)cc1C 10.1021/jm0611410
44191110 195625 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 371 5 1 5 4.4 COc1cc(Cl)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1F 10.1021/jm900302q
CHEMBL556255 195625 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 371 5 1 5 4.4 COc1cc(Cl)c(Nc2nc(Cl)cn([C@H](C)C3CC3)c2=O)cc1F 10.1021/jm900302q
46891340 6480 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 368 5 1 6 4.0 COc1cc(Cl)c(Nc2nc(C)nn([C@H](C)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2010.04.121
CHEMBL1082665 6480 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 368 5 1 6 4.0 COc1cc(Cl)c(Nc2nc(C)nn([C@H](C)C3CC3)c2=O)c(Cl)c1 10.1016/j.bmcl.2010.04.121
25114821 69997 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from rat CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from rat CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3cnc(OC(F)F)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939592 69997 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from rat CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from rat CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 390 6 0 6 4.2 CCC(CC)c1cc(C)n2nc(-c3cnc(OC(F)F)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
3520 3267 54 None 1 2 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/acs.jmedchem.5b01715
9821250 3267 54 None 1 2 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/acs.jmedchem.5b01715
CHEMBL309138 3267 54 None 1 2 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/acs.jmedchem.5b01715
42618227 189567 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 400 9 0 9 2.2 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL514465 189567 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 400 9 0 9 2.2 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
44191011 196247 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 459 7 1 6 4.8 COCC(COC)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
CHEMBL561757 196247 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration techniqueDisplacement of [125I]ovine-CRF from CRF1 receptor in rat frontal cortex by rapid filtration technique
ChEMBL 459 7 1 6 4.8 COCC(COC)n1cc(Cl)nc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)c1=O 10.1021/jm900302q
57400680 69996 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 354 5 0 6 3.6 CCC(CC)c1cc(C)n2nc(-c3cnc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939591 69996 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 354 5 0 6 3.6 CCC(CC)c1cc(C)n2nc(-c3cnc(OC)cc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
46891388 6485 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 383 6 1 7 3.5 CCOc1ccc(Nc2nc(C)nn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1082670 6485 0 None - 0 Rat 8.1 pIC50 = 8.1 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 383 6 1 7 3.5 CCOc1ccc(Nc2nc(C)nn([C@H](C)C3CC3)c2=O)c(C(F)(F)F)n1 10.1016/j.bmcl.2010.04.121
24964079 158964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 401 5 0 4 6.8 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(C#N)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL4096045 158964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 401 5 0 4 6.8 CCC(CC)c1ccc(Cl)c2nc(Oc3c(C)cc(C#N)cc3Cl)n(C)c12 10.1016/j.bmc.2016.11.011
57402455 70001 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 345 3 0 5 3.8 COc1ccc(-c2nn3c(C)cc(C(C)C)c3c(=O)n2C)c(Cl)c1 10.1016/j.bmc.2011.11.015
CHEMBL1939596 70001 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 345 3 0 5 3.8 COc1ccc(-c2nn3c(C)cc(C(C)C)c3c(=O)n2C)c(Cl)c1 10.1016/j.bmc.2011.11.015
24758076 69981 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 380 7 0 4 6.1 CCc1cc(OC)c(OC)cc1-c1nn2c(C)cc(C(CC)CC)c2cc1C 10.1016/j.bmc.2011.11.015
CHEMBL1939576 69981 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 380 7 0 4 6.1 CCc1cc(OC)c(OC)cc1-c1nn2c(C)cc(C(CC)CC)c2cc1C 10.1016/j.bmc.2011.11.015
58223396 127895 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 487 11 0 9 4.3 CCCN(CC1C2COCC21)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
CHEMBL3664607 127895 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 487 11 0 9 4.3 CCCN(CC1C2COCC21)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12 nan
58223425 127897 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 469 9 0 8 4.7 CCN(CC1C2COCC21)c1c(OC)nn2c(-c3c(OC)cc(C4CC4)cc3OC)csc12 nan
CHEMBL3664609 127897 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 469 9 0 8 4.7 CCN(CC1C2COCC21)c1c(OC)nn2c(-c3c(OC)cc(C4CC4)cc3OC)csc12 nan
10222402 64738 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 396 6 1 6 5.3 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCS2 10.1016/j.bmc.2011.07.055
CHEMBL1819062 64738 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 396 6 1 6 5.3 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4C)c(C)nn13)CCS2 10.1016/j.bmc.2011.07.055
42618173 189589 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 337 3 0 6 3.3 COc1ccc(-c2c(C)nn3c(N4CCCC4)nc(C)nc23)c(C)c1 10.1021/jm9000242
CHEMBL514649 189589 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 337 3 0 6 3.3 COc1ccc(-c2c(C)nn3c(N4CCCC4)nc(C)nc23)c(C)c1 10.1021/jm9000242
70684376 76619 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063382 76619 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmcl.2012.07.047
70684376 76619 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2063382 76619 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 428 8 0 5 5.9 CCN(CC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(Cl)cc12 10.1016/j.bmc.2012.09.028
57400683 70006 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 353 4 0 6 3.3 CCC(C)c1cc(C)n2nc(-c3ccc(N(C)C)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939600 70006 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 353 4 0 6 3.3 CCC(C)c1cc(C)n2nc(-c3ccc(N(C)C)nc3C)n(C)c(=O)c12 10.1016/j.bmc.2011.11.015
42618231 173475 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 326 4 0 7 2.6 CCN(C)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
CHEMBL453001 173475 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 326 4 0 7 2.6 CCN(C)c1nc(C)nc2c(-c3ccc(OC)nc3C)c(C)nn12 10.1021/jm900025h
53357409 130602 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 505 6 1 4 6.5 COc1ccc(-c2cc(C)n(C[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)n2)cc1 nan
CHEMBL3681385 130602 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 505 6 1 4 6.5 COc1ccc(-c2cc(C)n(C[C@H]3CC[C@H](NC(=O)c4cc(C(F)(F)F)ccc4Cl)CC3)n2)cc1 nan
3499 1448 28 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in adenylate cyclase activity was evaluatedInhibition of corticotropin releasing factor receptor mediated increase in adenylate cyclase activity was evaluated
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
9909468 1448 28 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in adenylate cyclase activity was evaluatedInhibition of corticotropin releasing factor receptor mediated increase in adenylate cyclase activity was evaluated
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
CHEMBL44698 1448 28 None - 1 Human 7.1 pIC50 = 7.1 Binding
Inhibition of corticotropin releasing factor receptor mediated increase in adenylate cyclase activity was evaluatedInhibition of corticotropin releasing factor receptor mediated increase in adenylate cyclase activity was evaluated
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
22177795 64750 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 362 5 1 4 5.4 CCC(CC)Nc1c2c(nc3c(-c4cc(C)ccc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819074 64750 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 362 5 1 4 5.4 CCC(CC)Nc1c2c(nc3c(-c4cc(C)ccc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
51352161 128812 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 505 11 0 9 5.7 CCCCN(c1c(SC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 nan
CHEMBL3669430 128812 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 505 11 0 9 5.7 CCCCN(c1c(SC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 nan
71460919 82609 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 501 11 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CCC4CC4)C4CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179187 82609 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 501 11 0 9 5.0 COCc1cc(OC)c(-c2csc3c(N(CCC4CC4)C4CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
25150450 175943 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 510 3 1 7 5.4 Cc1cc(-n2ccc(-c3nccs3)n2)c2[nH]c(=O)n(-c3ccc(C(F)(F)F)cc3C(F)(F)F)c2n1 10.1021/jm800743q
CHEMBL458780 175943 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 510 3 1 7 5.4 Cc1cc(-n2ccc(-c3nccs3)n2)c2[nH]c(=O)n(-c3ccc(C(F)(F)F)cc3C(F)(F)F)c2n1 10.1021/jm800743q
58896438 139502 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 1 4 5.6 CCCN(CCC)c1cccc2nc(Nc3ccc(C)cc3C)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793744 139502 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 1 4 5.6 CCCN(CCC)c1cccc2nc(Nc3ccc(C)cc3C)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3794592 139502 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 350 7 1 4 5.6 CCCN(CCC)c1cccc2nc(Nc3ccc(C)cc3C)n(C)c12 10.1021/acs.jmedchem.5b01715
56668634 64763 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 400 6 1 6 4.9 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)OCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819088 64763 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 400 6 1 6 4.9 CCC(CC)Nc1c2c(nc3c(-c4ccc(OC)cc4Cl)c(C)nn13)OCC2 10.1016/j.bmc.2011.07.055
68581422 174586 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 503 6 1 6 6.8 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3ccc(C#N)cc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4556873 174586 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 503 6 1 6 6.8 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3ccc(C#N)cc3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
44589257 174814 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 452 4 0 8 5.7 N#Cc1cc(-c2cccs2)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
CHEMBL456241 174814 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 452 4 0 8 5.7 N#Cc1cc(-c2cccs2)ccc1N1CCc2c(-n3ccc(-c4nccs4)n3)ccnc21 10.1021/jm800743q
21912341 97955 1 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1cc(OC(CC)CC)c(C)c(Oc2c(C)cc(C)cc2C)n1 10.1021/jm070578k
CHEMBL272619 97955 1 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1cc(OC(CC)CC)c(C)c(Oc2c(C)cc(C)cc2C)n1 10.1021/jm070578k
10160760 124070 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 444 6 0 5 5.1 CCc1nc2c(n1COCc1ccccc1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL363240 124070 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 444 6 0 5 5.1 CCc1nc2c(n1COCc1ccccc1)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
58223395 127865 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 13 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CCC(C)OC)CC4CC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664578 127865 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 489 13 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CCC(C)OC)CC4CC4)c(OC)nn23)c(OC)c1 nan
24768336 85528 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 414 9 1 7 4.1 CCCN(CCOC)c1cc(C)nc2c1NCCN2c1cc(OC)c(OC)cc1C 10.1021/jm0611410
CHEMBL227503 85528 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 414 9 1 7 4.1 CCCN(CCOC)c1cc(C)nc2c1NCCN2c1cc(OC)c(OC)cc1C 10.1021/jm0611410
44589202 175956 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 438 3 0 7 5.0 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
CHEMBL458824 175956 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 438 3 0 7 5.0 N#Cc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
21912341 97955 1 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1cc(OC(CC)CC)c(C)c(Oc2c(C)cc(C)cc2C)n1 10.1021/jm070578k
CHEMBL272619 97955 1 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1cc(OC(CC)CC)c(C)c(Oc2c(C)cc(C)cc2C)n1 10.1021/jm070578k
44589303 176019 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 375 4 0 7 4.1 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)cc1 10.1021/jm800743q
CHEMBL458980 176019 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 375 4 0 7 4.1 COc1ccc(N2CCc3c(-n4ccc(-c5nccs5)n4)ccnc32)cc1 10.1021/jm800743q
10159424 122813 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 424 5 0 5 4.6 CCc1nc2c(n1Cc1ccccc1C)C(=O)N(C)CN2c1ccc(OC)cc1Cl 10.1021/jm049787k
CHEMBL360532 122813 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 424 5 0 5 4.6 CCc1nc2c(n1Cc1ccccc1C)C(=O)N(C)CN2c1ccc(OC)cc1Cl 10.1021/jm049787k
58223376 127899 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 513 11 0 9 4.7 COCc1cc(OC)c(-c2csc3c(N(CC4CCC4)CC4C5COCC54)c(OC)nn23)c(OC)c1 nan
CHEMBL3664610 127899 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 513 11 0 9 4.7 COCc1cc(OC)c(-c2csc3c(N(CC4CCC4)CC4C5COCC54)c(OC)nn23)c(OC)c1 nan
70682293 76608 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 436 10 0 5 6.3 CCCN(CCC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063369 76608 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 436 10 0 5 6.3 CCCN(CCC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
70692846 76612 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 460 10 0 5 6.3 COCc1cc(OC)c(-c2nc3c(C)ccc(N(CC4CC4)CC4CC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
CHEMBL2063373 76612 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 460 10 0 5 6.3 COCc1cc(OC)c(-c2nc3c(C)ccc(N(CC4CC4)CC4CC4)c3cc2C)c(OC)c1 10.1016/j.bmcl.2012.07.047
70682293 76608 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 436 10 0 5 6.3 CCCN(CCC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2063369 76608 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 436 10 0 5 6.3 CCCN(CCC)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
70688432 75902 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 375 7 1 3 6.8 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)cc12 10.1016/j.bmcl.2012.05.066
CHEMBL2049193 75902 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 375 7 1 3 6.8 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)c(C)cc12 10.1016/j.bmcl.2012.05.066
67117558 139953 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 364 6 2 7 2.6 COc1nc(C)c(Nc2nc(Cl)cn([C@H](CO)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
CHEMBL3799741 139953 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 364 6 2 7 2.6 COc1nc(C)c(Nc2nc(Cl)cn([C@H](CO)C3CC3)c2=O)cc1C 10.1016/j.bmcl.2016.03.067
53357410 126538 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 360 4 1 4 3.8 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
CHEMBL3652116 126538 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 360 4 1 4 3.8 Cc1cc(C)n(C[C@H]2CC[C@H](NC(=O)c3cc(Cl)cnc3C)CC2)n1 nan
58223512 127852 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 507 12 0 9 5.0 CCOCc1cc(OC)c(-c2csc3c(N(CCCF)C4CCOCC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664565 127852 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 507 12 0 9 5.0 CCOCc1cc(OC)c(-c2csc3c(N(CCCF)C4CCOCC4)c(OC)nn23)c(OC)c1 nan
90654176 127888 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 515 12 0 9 5.3 CCOc1nn2c(-c3c(OC)cc(COC)cc3OC)csc2c1N(CC1CCOCC1)CC1CC1 nan
CHEMBL3664600 127888 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 515 12 0 9 5.3 CCOc1nn2c(-c3c(OC)cc(COC)cc3OC)csc2c1N(CC1CCOCC1)CC1CC1 nan
58223489 128808 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 480 9 0 9 4.1 COc1cc(C#N)cc(OC)c1-c1csc2c(N(CC3CC3)CC3C4COCC43)c(OC)nn12 nan
CHEMBL3669427 128808 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 480 9 0 9 4.1 COc1cc(C#N)cc(OC)c1-c1csc2c(N(CC3CC3)CC3C4COCC43)c(OC)nn12 nan
70684375 76613 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 424 9 0 6 4.8 COCCN(C)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
CHEMBL2063374 76613 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrsDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs
ChEMBL 424 9 0 6 4.8 COCCN(C)c1ccc(C)c2nc(-c3c(OC)cc(COC)cc3OC)c(C)cc12 10.1016/j.bmcl.2012.07.047
145967853 165004 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 410 3 1 5 5.8 CCN(O)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
CHEMBL4225843 165004 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 410 3 1 5 5.8 CCN(O)c1ccc(Cl)c2nc3n(c12)CCCN3c1ccc(Cl)cc1Cl 10.1016/j.bmc.2018.01.020
44589318 177685 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 494 3 1 6 4.8 Cc1cc(-n2ccc(-n3cc[nH]c3=O)n2)c2c(n1)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1021/jm800744m
CHEMBL464185 177685 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cellsDisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells
ChEMBL 494 3 1 6 4.8 Cc1cc(-n2ccc(-n3cc[nH]c3=O)n2)c2c(n1)N(c1ccc(C(F)(F)F)cc1C(F)(F)F)CC2 10.1021/jm800744m
145955820 162674 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 355 4 1 6 4.0 CCN(CC)c1nc(C)nc2c1sc(=N)n2-c1c(C)cc(C)cc1C 10.1016/j.ejmech.2017.07.016
CHEMBL4170184 162674 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting methodDisplacement of [125I]-Tyr0-sauvagine from human CRFR1 expressed in HEK293 cell membrane homogenates after 120 mins by gamma counting method
ChEMBL 355 4 1 6 4.0 CCN(CC)c1nc(C)nc2c1sc(=N)n2-c1c(C)cc(C)cc1C 10.1016/j.ejmech.2017.07.016
10272004 166244 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 394 6 0 4 5.5 CCCC(CCC)n1cnc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL426791 166244 0 None - 0 Rat 6.1 pIC50 = 6.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 394 6 0 4 5.5 CCCC(CCC)n1cnc2c1C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
10111139 64752 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 392 6 1 5 5.4 CCC(CC)Nc1c2c(nc3c(-c4c(C)cc(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819076 64752 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 392 6 1 5 5.4 CCC(CC)Nc1c2c(nc3c(-c4c(C)cc(OC)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
9819381 97698 3 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1c(OC(CC)CC)cc(C)nc1Oc1c(C)cc(C)cc1C 10.1021/jm070578k
CHEMBL271324 97698 3 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1c(OC(CC)CC)cc(C)nc1Oc1c(C)cc(C)cc1C 10.1021/jm070578k
9819381 97698 3 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1c(OC(CC)CC)cc(C)nc1Oc1c(C)cc(C)cc1C 10.1021/jm070578k
CHEMBL271324 97698 3 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 341 7 0 3 6.2 CCc1c(OC(CC)CC)cc(C)nc1Oc1c(C)cc(C)cc1C 10.1021/jm070578k
58280029 139756 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 528 9 2 10 4.6 COc1ccc(NC(=O)OC[C@H](C2CC2)n2cc(Cl)nc(Nc3cc(C)c(OC)nc3C)c2=O)c(C)n1 10.1016/j.bmcl.2016.03.067
CHEMBL3798497 139756 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysisDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate after 2 hrs by gamma counting analysis
ChEMBL 528 9 2 10 4.6 COc1ccc(NC(=O)OC[C@H](C2CC2)n2cc(Cl)nc(Nc3cc(C)c(OC)nc3C)c2=O)c(C)n1 10.1016/j.bmcl.2016.03.067
46891158 6494 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 337 5 1 6 3.5 CCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(C#N)cc2C)c1=O 10.1016/j.bmcl.2010.04.121
CHEMBL1082706 6494 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 337 5 1 6 3.5 CCC(C1CC1)n1nc(C)nc(Nc2cc(C)c(C#N)cc2C)c1=O 10.1016/j.bmcl.2010.04.121
44190243 196103 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 351 5 1 4 5.0 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cccc2Cl)c1=O 10.1021/jm900301y
CHEMBL560896 196103 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 351 5 1 4 5.0 CC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)cccc2Cl)c1=O 10.1021/jm900301y
70909805 139314 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 434 8 1 5 6.6 CCCN(CCC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3792517 139314 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 434 8 1 5 6.6 CCCN(CCC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1021/acs.jmedchem.5b01715
70909805 139314 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 434 8 1 5 6.6 CCCN(CCC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
CHEMBL3792517 139314 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 434 8 1 5 6.6 CCCN(CCC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2016.11.011
127030314 139389 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 406 6 1 5 5.8 CCN(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2018.01.020
CHEMBL3793277 139389 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting methodDisplacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes after 1.5 hrs by liquid scintillation counting method
ChEMBL 406 6 1 5 5.8 CCN(CC)c1ccc(Cl)c2nc(Nc3c(C)cc(Cl)cc3OC)n(C)c12 10.1016/j.bmc.2018.01.020
57392001 69987 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 367 6 0 5 4.7 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC)c(=O)c12 10.1016/j.bmc.2011.11.015
CHEMBL1939582 69987 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counterDisplacement of [125I]CRF from human CRF1 receptor expressed in CHO-K1 cells after 2 hrs by gamma counter
ChEMBL 367 6 0 5 4.7 CCC(CC)c1cc(C)n2nc(-c3ccc(OC)cc3C)n(CC)c(=O)c12 10.1016/j.bmc.2011.11.015
42618174 193334 0 None - 1 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 385 8 1 8 2.8 COCC(COC)Nc1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
CHEMBL524616 193334 0 None - 1 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyr0-ovine CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 385 8 1 8 2.8 COCC(COC)Nc1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm9000242
24768324 97660 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 391 6 0 3 6.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1Br 10.1021/jm070578k
CHEMBL271125 97660 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 391 6 0 3 6.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1Br 10.1021/jm070578k
9820041 158232 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 355 8 0 3 6.6 CCCc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
CHEMBL408824 158232 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 355 8 0 3 6.6 CCCc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
24768324 97660 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 391 6 0 3 6.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1Br 10.1021/jm070578k
CHEMBL271125 97660 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 391 6 0 3 6.4 CCC(CC)Oc1cc(C)nc(Oc2c(C)cc(C)cc2C)c1Br 10.1021/jm070578k
9820041 158232 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 355 8 0 3 6.6 CCCc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
CHEMBL408824 158232 0 None - 0 Rat 8.0 pIC50 = 8.0 Binding
Displacement of [125]oCRF from rat cortex CRF1 receptorDisplacement of [125]oCRF from rat cortex CRF1 receptor
ChEMBL 355 8 0 3 6.6 CCCc1cc(C)c(Oc2nc(C)cc(OC(CC)CC)c2C)c(C)c1 10.1021/jm070578k
24768334 144578 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 386 8 1 8 3.4 CCCCN(CC)c1nc(C)nc2c1NCCN2c1ccc(OC)nc1OC 10.1021/jm0611410
CHEMBL390763 144578 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 386 8 1 8 3.4 CCCCN(CC)c1nc(C)nc2c1NCCN2c1ccc(OC)nc1OC 10.1021/jm0611410
46891089 6820 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 404 6 1 6 4.6 Cc1nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
CHEMBL1083946 6820 0 None - 0 Rat 8.0 pIC50 = 8 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 404 6 1 6 4.6 Cc1nc(Nc2c(Cl)cc(OC(F)F)cc2Cl)c(=O)n(C(C)C2CC2)n1 10.1016/j.bmcl.2010.04.121
70690481 75905 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 429 6 1 4 6.6 Cc1cc(C)c(Nc2nc3cccc(N(CC4CC4)C4CCOCC4)c3cc2C)c(C)c1 10.1016/j.bmcl.2012.05.066
CHEMBL2049196 75905 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 429 6 1 4 6.6 Cc1cc(C)c(Nc2nc3cccc(N(CC4CC4)C4CCOCC4)c3cc2C)c(C)c1 10.1016/j.bmcl.2012.05.066
58801667 77564 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 481 11 0 7 5.4 CCCN(CC1CCOCC1)c1c(CC)nn2c(-c3c(OC)cc(COC)cc3OC)cccc12 10.1021/jm300259r
CHEMBL2087572 77564 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 481 11 0 7 5.4 CCCN(CC1CCOCC1)c1c(CC)nn2c(-c3c(OC)cc(COC)cc3OC)cccc12 10.1021/jm300259r
46881866 8012 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 395 8 1 9 2.4 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)nc(OC)nc2OC)c1=O 10.1016/j.bmcl.2010.01.129
CHEMBL1090740 8012 0 None - 0 Rat 7.1 pIC50 = 7.1 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 395 8 1 9 2.4 COC[C@H](C1CC1)n1cc(Cl)nc(Nc2c(C)nc(OC)nc2OC)c1=O 10.1016/j.bmcl.2010.01.129
58896512 172977 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 556 7 1 7 6.3 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(S(C)(=O)=O)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
CHEMBL4517763 172977 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount methodDisplacement of ovine [125I-Tyr0]-CRF from human CRF1 receptor expressed in CHO cell membrane measured after 1.5 hrs by TopCount method
ChEMBL 556 7 1 7 6.3 COc1cc(Br)cc(C)c1Nc1nc2cccc(N(c3cccc(S(C)(=O)=O)c3)C(C)C)c2n1C 10.1016/j.bmc.2016.08.005
10205141 63465 0 None - 0 Rat 5.1 pIC50 = 5.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 464 4 0 4 6.1 CCc1nc2c(n1Cc1cccc3ccccc13)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
CHEMBL179826 63465 0 None - 0 Rat 5.1 pIC50 = 5.1 Binding
Inhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptorInhibition of [125I]- Ovine CRF binding to rat frontal cortex corticotropin releasing factor 1 receptor
ChEMBL 464 4 0 4 6.1 CCc1nc2c(n1Cc1cccc3ccccc13)C(=O)N(C)CN2c1ccc(Cl)cc1Cl 10.1021/jm049787k
71453736 82612 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 489 10 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CC(C)C)C4CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
CHEMBL2179190 82612 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 489 10 0 9 4.9 COCc1cc(OC)c(-c2csc3c(N(CC(C)C)C4CCOCC4)c(OC)nn23)c(OC)c1 10.1021/jm300864p
42618215 184094 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 413 9 0 9 2.3 COCCN(CCOC)c1nc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm900025h
CHEMBL482544 184094 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma countingDisplacement of [125I]Tyro-rat/human CRF from CRF1 receptor in rat cortical membrane by gamma counting
ChEMBL 413 9 0 9 2.3 COCCN(CCOC)c1nc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm900025h
44190338 196123 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 453 9 1 6 5.4 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OCc3ccccc3)cc2C)c1=O 10.1021/jm900301y
CHEMBL561034 196123 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
Displacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma countingDisplacement of [125I]Tyr-ovine-CRF from CRF1 receptor in rat frontal cortex homogenate by gamma counting
ChEMBL 453 9 1 6 5.4 COC[C@@H](C1CC1)n1cc(Cl)nc(Nc2cc(C)c(OCc3ccccc3)cc2C)c1=O 10.1021/jm900301y
51352160 127835 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 11 0 10 4.1 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4COCOC4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664548 127835 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 503 11 0 10 4.1 COCc1cc(OC)c(-c2csc3c(N(CC4CC4)CC4COCOC4)c(OC)nn23)c(OC)c1 nan
10377 1179 27 None -1 2 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2011.02.086
9818802 1179 27 None -1 2 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2011.02.086
CHEMBL270738 1179 27 None -1 2 Human 7.0 pIC50 = 7.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2011.02.086
11280845 126836 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 393 7 1 6 3.9 CCN(CCCC#N)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1021/jm049737f
CHEMBL365511 126836 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 393 7 1 6 3.9 CCN(CCCC#N)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1021/jm049737f
58223470 127830 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 563 12 0 10 6.3 COCc1cc(OC)c(-c2c(SC)sc3c(N(CC4CCOCC4)CC4CC4)c(SC)nn23)c(OC)c1 nan
CHEMBL3664543 127830 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 563 12 0 10 6.3 COCc1cc(OC)c(-c2c(SC)sc3c(N(CC4CCOCC4)CC4CC4)c(SC)nn23)c(OC)c1 nan
23567868 64748 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 366 5 1 4 5.2 CCC(CC)Nc1c2c(nc3c(-c4ccc(F)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
CHEMBL1819072 64748 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 366 5 1 4 5.2 CCC(CC)Nc1c2c(nc3c(-c4ccc(F)cc4C)c(C)nn13)CCC2 10.1016/j.bmc.2011.07.055
44589348 176026 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 432 3 0 6 4.9 N#Cc1ccc(N2CCc3c(-n4ccc(-c5ccccn5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
CHEMBL459006 176026 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPADisplacement of [125I]sauvagine from human recombinant CRF1 receptor expressed in CHO cells by SPA
ChEMBL 432 3 0 6 4.9 N#Cc1ccc(N2CCc3c(-n4ccc(-c5ccccn5)n4)ccnc32)c(C(F)(F)F)c1 10.1021/jm800743q
46891190 6426 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 339 5 1 7 2.9 COc1cc(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C)cc1C#N 10.1016/j.bmcl.2010.04.121
CHEMBL1082401 6426 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr-ovine CRF from rat CRF1 receptorDisplacement of [125I]Tyr-ovine CRF from rat CRF1 receptor
ChEMBL 339 5 1 7 2.9 COc1cc(Nc2nc(C)nn(C(C)C3CC3)c2=O)c(C)cc1C#N 10.1016/j.bmcl.2010.04.121
67363460 130590 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 468 7 3 3 5.4 O=C(O)Cc1ccc(NC[C@H]2CC[C@@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)cc1 nan
CHEMBL3681373 130590 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 468 7 3 3 5.4 O=C(O)Cc1ccc(NC[C@H]2CC[C@@H](NC(=O)c3cc(C(F)(F)F)ccc3Cl)CC2)cc1 nan
58223507 127853 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 537 11 0 9 5.1 COCc1cc(OC)c(-c2csc3c(N(CC4CCOC4)CC4CC(F)(F)C4)c(OC)nn23)c(OC)c1 nan
CHEMBL3664566 127853 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 537 11 0 9 5.1 COCc1cc(OC)c(-c2csc3c(N(CC4CCOC4)CC4CC(F)(F)C4)c(OC)nn23)c(OC)c1 nan
24768330 85576 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 383 7 1 6 3.8 CCCCN(CC)c1nc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1021/jm0611410
CHEMBL228110 85576 0 None - 0 Rat 7.0 pIC50 = 7.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 383 7 1 6 3.8 CCCCN(CC)c1nc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1021/jm0611410
53357797 130610 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 449 5 2 4 4.7 O=C(N[C@H]1CC[C@H](Cn2cc(Cl)c(CO)n2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
CHEMBL3681393 130610 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.Homogeneous Time-Resolved Fluorescence Assay: Chinese hamster ovary (CHO) cells expressing either the human or rat recombinant CRF-1 or human CRF-2alpha (Chen et al, Proc Natl Acad Sci USA 90, 8967-8971, 1993; Liaw et al, Endocrinology 137, 72-77, 1996) are propagated in Dulbecco's modified Eagle medium supplemented with 10% foetal calf serum, non-essential amino acids, 100 U/ml penicillin, 100 mg/l streptomycin and 1 g/l geneticin. CHO cells expressing the rat CRF-2beta receptor (Wu et al, Endocrinology 148, 1675-1687, 2007) are propagated in HAM's-F12 Glutamax supplemented with 10% foetal calf serum, 100 IU/ml penicillin, 100 mg/l streptomycin, 600 ug/ml hygromycin, 10 ug/ml blasticidin and induced with 1 ug/ml of tetracyclin for 24 hours prior to experimentation. For cyclic AMP determinations the Homogeneous Time-Resolved Fluoresce (HTRF) CAMP dynamic 2 kit (Cisbio International, France) was used as per manufacturers' instructions.
ChEMBL 449 5 2 4 4.7 O=C(N[C@H]1CC[C@H](Cn2cc(Cl)c(CO)n2)CC1)c1cc(C(F)(F)F)ccc1Cl nan
58896424 139414 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 392 8 1 4 6.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)n(C(C)C)c12 10.1021/acs.jmedchem.5b01715
CHEMBL3793781 139414 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 392 8 1 4 6.9 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)n(C(C)C)c12 10.1021/acs.jmedchem.5b01715
22178115 64743 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 392 7 1 5 5.4 CCc1nn2c(NC(CC)CC)c3c(nc2c1-c1ccc(OC)cc1C)CCC3 10.1016/j.bmc.2011.07.055
CHEMBL1819067 64743 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 392 7 1 5 5.4 CCc1nn2c(NC(CC)CC)c3c(nc2c1-c1ccc(OC)cc1C)CCC3 10.1016/j.bmc.2011.07.055
54580961 60650 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 408 8 0 5 5.3 CCCCN(CCCC)c1nc2c(c(-c3c(C)cc(C)cc3C)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
CHEMBL1760254 60650 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cellsDisplacement of ovine [125I]CRF from human CRF1 receptor expressed in CHO cells
ChEMBL 408 8 0 5 5.3 CCCCN(CCCC)c1nc2c(c(-c3c(C)cc(C)cc3C)cn2C)c(=O)n1C 10.1016/j.bmcl.2011.02.086
60155889 77575 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 527 11 1 9 4.6 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4(O)CC4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
CHEMBL2087797 77575 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counterDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by liquid scintillation counter
ChEMBL 527 11 1 9 4.6 COCc1cc(OC)c(-c2cccc3c(N(CC4CCOCC4)CC4(O)CC4)c(SC)nn23)c(OC)c1 10.1021/jm300259r
57912441 82608 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 475 10 0 9 4.6 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
CHEMBL2179186 82608 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assayDisplacement of [125I]CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation proximity assay
ChEMBL 475 10 0 9 4.6 CCCN(c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12)C1CCOCC1 10.1021/jm300864p
58223406 128809 0 None - 0 Human 7.0 pIC50 = 7 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 468 9 0 9 4.1 CCCN(CC1C2COCC21)c1c(OC)nn2c(-c3c(OC)cc(C#N)cc3OC)csc12 nan
CHEMBL3669428 128809 0 None - 0 Human 7.0 pIC50 = 7 Binding
Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.Binding Assay: A binding competition experiment with CRF was conducted by the SPA (GE Healthcare) method using a 96-well plate.
ChEMBL 468 9 0 9 4.1 CCCN(CC1C2COCC21)c1c(OC)nn2c(-c3c(OC)cc(C#N)cc3OC)csc12 nan
71456848 81510 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 394 7 0 5 5.4 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(C)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
CHEMBL2160159 81510 0 None - 0 Human 7.0 pIC50 = 7 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation countingDisplacement of [125I]-CRF from human CRF1 receptor expressed in HEK293 cells after 2 hrs by scintillation counting
ChEMBL 394 7 0 5 5.4 CCN(CC)c1ccc(OC)c2nc(-c3c(OC)cc(C)cc3OC)c(C)cc12 10.1016/j.bmc.2012.09.028
58896475 139366 0 None - 0 Human 6.0 pIC50 = 6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 351 7 1 4 6.1 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)oc12 10.1021/acs.jmedchem.5b01715
CHEMBL3793059 139366 0 None - 0 Human 6.0 pIC50 = 6 Binding
Displacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting methodDisplacement of [125I]-CRF from human CRF1 receptor expressed in CHO cellular membrane fraction after 1.5 hrs by liquid scintillation counting method
ChEMBL 351 7 1 4 6.1 CCCN(CCC)c1cccc2nc(Nc3c(C)cc(C)cc3C)oc12 10.1021/acs.jmedchem.5b01715
9884878 173025 18 None - 1 Human 9.6 pKd = 9.6 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2011.08.040
CHEMBL45187 173025 18 None - 1 Human 9.6 pKd = 9.6 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2011.08.040
54591779 66030 0 None - 1 Human 9.5 pKd = 9.5 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 429 8 1 7 4.6 COc1cc(OC(F)F)ccc1-n1c(C)nc2c(NC(C3CC3)C3CC3)nc(C)nc21 10.1016/j.bmcl.2011.08.040
CHEMBL1836947 66030 0 None - 1 Human 9.5 pKd = 9.5 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 429 8 1 7 4.6 COc1cc(OC(F)F)ccc1-n1c(C)nc2c(NC(C3CC3)C3CC3)nc(C)nc21 10.1016/j.bmcl.2011.08.040
3520 3267 54 None 1 2 Human 9.5 pKd = 9.5 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2011.08.040
9821250 3267 54 None 1 2 Human 9.5 pKd = 9.5 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2011.08.040
CHEMBL309138 3267 54 None 1 2 Human 9.5 pKd = 9.5 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2011.08.040
44545165 66028 0 None - 1 Human 9.4 pKd = 9.4 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 433 7 1 6 5.3 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3Cl)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836945 66028 0 None - 1 Human 9.4 pKd = 9.4 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 433 7 1 6 5.3 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3Cl)c2n1 10.1016/j.bmcl.2011.08.040
54591854 66015 0 None - 1 Human 7.9 pKd = 7.9 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 363 6 1 6 4.0 COc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
CHEMBL1836932 66015 0 None - 1 Human 7.9 pKd = 7.9 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 363 6 1 6 4.0 COc1ccc(-n2c(C)nc3c(NC(C4CC4)C4CC4)nc(C)nc32)cc1 10.1016/j.bmcl.2011.08.040
45485040 197284 0 None - 1 Human 7.9 pKd = 7.9 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 383 8 0 7 3.6 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2011.08.040
CHEMBL568606 197284 0 None - 1 Human 7.9 pKd = 7.9 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 383 8 0 7 3.6 CCCN(CCOC)c1nc(C)nc2c1c(C)nn2-c1ccc(OC)cc1C 10.1016/j.bmcl.2011.08.040
44545161 66027 0 None - 1 Human 8.5 pKd = 8.5 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 399 7 1 6 4.6 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL1836944 66027 0 None - 1 Human 8.5 pKd = 8.5 Binding
Binding affinity to recombinant human CRF1 receptor expressed in CHO cellsBinding affinity to recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 399 7 1 6 4.6 Cc1nc(NC(C2CC2)C2CC2)c2nc(C)n(-c3ccc(OC(F)F)cc3)c2n1 10.1016/j.bmcl.2011.08.040
CHEMBL4299295 213562 0 None 1 2 Human 9.8 pKi = 9.8 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127033542 138622 0 None 2 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3960 128 56 50 -10.4 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775796 138622 0 None 2 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3960 128 56 50 -10.4 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127032315 138428 0 None 1 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3880 126 55 49 -10.4 CCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3774395 138428 0 None 1 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3880 126 55 49 -10.4 CCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL4299341 213570 0 None -1 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@H](CC(N)=O)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C(N)=O)[C@H](C)CC)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
11546255 188117 0 None 12022 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 419 5 0 7 4.9 CCC(CC)c1cc(C)nn2c(-c3sc(N4CCOCC4)nc3Cl)c(C)nc12 10.1016/j.bmcl.2008.07.063
CHEMBL498311 188117 0 None 12022 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 419 5 0 7 4.9 CCC(CC)c1cc(C)nn2c(-c3sc(N4CCOCC4)nc3Cl)c(C)nc12 10.1016/j.bmcl.2008.07.063
127031741 138496 0 None 1 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4028 129 57 50 -9.6 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@H](Cc2ccc(NC(N)=O)cc2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3774868 138496 0 None 1 2 Human 9.7 pKi = 9.7 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4028 129 57 50 -9.6 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@H](Cc2ccc(NC(N)=O)cc2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127033842 138517 0 None 8 2 Human 9.6 pKi = 9.6 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4000 127 56 51 -10.2 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc2cccs2)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
CHEMBL3775030 138517 0 None 8 2 Human 9.6 pKi = 9.6 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4000 127 56 51 -10.2 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc2cccs2)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
127032010 138471 0 None 9 2 Human 9.6 pKi = 9.6 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4000 127 56 51 -10.2 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc2ccsc2)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
CHEMBL3774682 138471 0 None 9 2 Human 9.6 pKi = 9.6 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4000 127 56 51 -10.2 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc2ccsc2)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
127032315 138428 0 None 1 2 Human 9.6 pKi = 9.6 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3880 126 55 49 -10.4 CCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3774395 138428 0 None 1 2 Human 9.6 pKi = 9.6 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3880 126 55 49 -10.4 CCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL4299349 213572 0 None 1 2 Human 9.5 pKi = 9.5 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)N[C@@](C)(CC(C)C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL4299348 213571 0 None 1 2 Human 9.5 pKi = 9.5 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)NC(C)(CC(C)C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127033542 138622 0 None 2 2 Human 9.5 pKi = 9.5 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3960 128 56 50 -10.4 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775796 138622 0 None 2 2 Human 9.5 pKi = 9.5 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3960 128 56 50 -10.4 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127031439 138599 0 None 5 2 Human 9.5 pKi = 9.5 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3994 127 56 50 -10.3 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
CHEMBL3775621 138599 0 None 5 2 Human 9.5 pKi = 9.5 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3994 127 56 50 -10.3 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
CHEMBL4299340 213569 0 None -1 2 Human 9.5 pKi = 9.5 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC(=O)C(CCCC)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@H](C)C(=O)N1)C(=O)N[C@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C(N)=O)[C@H](C)CC 10.1021/acs.jmedchem.5b00926
10111093 118751 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 391 6 0 5 5.3 CCCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL341820 118751 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 391 6 0 5 5.3 CCCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
127031736 138606 0 None 1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3876 124 56 50 -12.4 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775678 138606 0 None 1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3876 124 56 50 -12.4 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127032314 138620 0 None -1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3902 125 55 49 -10.2 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](C)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775778 138620 0 None -1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3902 125 55 49 -10.2 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](C)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL4299352 213573 0 None 2 2 Human 9.4 pKi = 9.4 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL4299286 213559 0 None 2 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(Cc2ccccc2)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(Cc1ccccc1)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL4299295 213562 0 None 1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127031441 138576 0 None 1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3900 124 55 49 -10.7 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(Cc2ccccc2)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775437 138576 0 None 1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3900 124 55 49 -10.7 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(Cc2ccccc2)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127033544 138625 0 None 2 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4044 127 56 50 -9.1 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc2ccc3ccccc3c2)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
CHEMBL3775812 138625 0 None 2 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4044 127 56 50 -9.1 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc2ccc3ccccc3c2)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
9908879 10080 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 398 6 0 2 7.1 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL115389 10080 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 398 6 0 2 7.1 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
127031132 138463 0 None 7 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4044 127 56 50 -9.1 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc2cccc3ccccc23)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
CHEMBL3774594 138463 0 None 7 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4044 127 56 50 -9.1 CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc2cccc3ccccc23)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
127031129 138617 0 None -1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3936 130 55 49 -8.8 CCCCCCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3775761 138617 0 None -1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3936 130 55 49 -8.8 CCCCCCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL4299308 213564 0 None 1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC(=O)C(CCCC)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N1)C(=O)N[C@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C(N)=O)[C@H](C)CC 10.1021/acs.jmedchem.5b00926
127029856 138540 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3866 125 55 49 -10.8 CCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3775192 138540 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3866 125 55 49 -10.8 CCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
10715520 119336 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL344223 119336 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
127030817 138507 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3824 122 55 49 -12.0 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3774939 138507 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3824 122 55 49 -12.0 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
9909978 10038 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
CHEMBL115142 10038 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
9909978 10038 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL115142 10038 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
127031129 138617 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3936 130 55 49 -8.8 CCCCCCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3775761 138617 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3936 130 55 49 -8.8 CCCCCCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
127033847 138490 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3880 124 55 49 -10.7 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C(=O)N[C@H](C(N)=O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b00926
CHEMBL3774836 138490 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3880 124 55 49 -10.7 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C(=O)N[C@H](C(N)=O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b00926
127029856 138540 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3866 125 55 49 -10.8 CCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3775192 138540 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3866 125 55 49 -10.8 CCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
127031738 138446 0 None 1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3903 125 55 49 -9.6 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3774485 138446 0 None 1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3903 125 55 49 -9.6 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
127031126 138478 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3838 123 55 49 -11.6 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)CC)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3774742 138478 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3838 123 55 49 -11.6 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)CC)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL4299297 213563 0 None -1 2 Human 9.2 pKi = 9.2 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C(=O)N[C@H](C(N)=O)[C@@H](C)CC)C(C)C 10.1021/acs.jmedchem.5b00926
10294626 32134 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 403 6 0 5 5.3 CCCN(CC1CC1)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL140894 32134 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 403 6 0 5 5.3 CCCN(CC1CC1)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
44347388 114551 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 434 7 0 5 6.4 CCCN(CC1CC1)c1cc(SC)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL333735 114551 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 434 7 0 5 6.4 CCCN(CC1CC1)c1cc(SC)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.019
127033848 138443 0 None -2 2 Human 9.1 pKi = 9.1 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3852 124 55 49 -11.2 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)CCC)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3774465 138443 0 None -2 2 Human 9.1 pKi = 9.1 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3852 124 55 49 -11.2 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)CCC)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL4299286 213559 0 None 2 2 Human 9.1 pKi = 9.1 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(Cc2ccccc2)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(Cc1ccccc1)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL4299340 213569 0 None -1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC(=O)C(CCCC)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@H](C)C(=O)N1)C(=O)N[C@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C(N)=O)[C@H](C)CC 10.1021/acs.jmedchem.5b00926
44392711 123546 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 437 6 0 5 5.7 CCCN(CC1CC1)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL361782 123546 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 437 6 0 5 5.7 CCCN(CC1CC1)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
10552787 120735 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 480 7 1 6 5.4 CCCC(CCC)Nc1nc(C)nc2c1nnn2-c1ccc(Br)cc1Br 10.1021/jm980224g
CHEMBL354886 120735 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 480 7 1 6 5.4 CCCC(CCC)Nc1nc(C)nc2c1nnn2-c1ccc(Br)cc1Br 10.1021/jm980224g
CHEMBL439883 213849 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [125I]-Tyr0-sauvagine from CRF1 receptor (unknown origin)Displacement of [125I]-Tyr0-sauvagine from CRF1 receptor (unknown origin)
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1016/j.bmcl.2015.10.010
CHEMBL439883 213849 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@@H]1CCC(=O)N1)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(=O)O 10.1016/j.bmcl.2015.10.010
127033261 138474 0 None 1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3992 134 55 49 -7.3 CCCCCCCCCCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3774713 138474 0 None 1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3992 134 55 49 -7.3 CCCCCCCCCCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
177990 426 23 None -1 2 Human 9.1 pKi = 9.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm980224g
3489 426 23 None -1 2 Human 9.1 pKi = 9.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm980224g
CHEMBL296641 426 23 None -1 2 Human 9.1 pKi = 9.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm980224g
10694584 58732 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 443 7 0 5 5.9 CCCCN(CC)c1nc(C)nc2c1nc(C)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168554 58732 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 443 7 0 5 5.9 CCCCN(CC)c1nc(C)nc2c1nc(C)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10388138 9999 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 432 9 0 4 7.0 CCCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL114912 9999 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 432 9 0 4 7.0 CCCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9821586 168103 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity towards cloned human CRF1 receptor expressed in CHO cells using [125I]-o-CRF as the radioligandBinding affinity towards cloned human CRF1 receptor expressed in CHO cells using [125I]-o-CRF as the radioligand
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL432800 168103 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity towards cloned human CRF1 receptor expressed in CHO cells using [125I]-o-CRF as the radioligandBinding affinity towards cloned human CRF1 receptor expressed in CHO cells using [125I]-o-CRF as the radioligand
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
9821586 168103 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/j.bmcl.2007.12.050
CHEMBL432800 168103 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/j.bmcl.2007.12.050
10251024 168416 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 410 8 0 4 6.2 CCCN(CCCCF)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(00)00071-8
CHEMBL434882 168416 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 410 8 0 4 6.2 CCCN(CCCCF)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(00)00071-8
CHEMBL4299335 213568 0 None -1 2 Human 9.0 pKi = 9.0 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(Cc1ccccc1)C(=O)N[C@@H](C(N)=O)[C@H](C)CC 10.1021/acs.jmedchem.5b00926
177990 426 23 None 1 2 Rat 9.0 pKi = 9 Binding
Affinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brainAffinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brain
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm034077k
3489 426 23 None 1 2 Rat 9.0 pKi = 9 Binding
Affinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brainAffinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brain
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm034077k
CHEMBL296641 426 23 None 1 2 Rat 9.0 pKi = 9 Binding
Affinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brainAffinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brain
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm034077k
44341921 10294 0 None - 1 Human 9.0 pKi = 9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 444 9 0 4 7.0 CCCCCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL116171 10294 0 None - 1 Human 9.0 pKi = 9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 444 9 0 4 7.0 CCCCCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9998661 57948 0 None - 1 Rat 9.0 pKi = 9 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 360 3 0 4 4.4 COc1cc(Br)c(-n2ccc3c(C)cc(C)nc32)c(OC)c1 10.1021/jm980223o
CHEMBL167241 57948 0 None - 1 Rat 9.0 pKi = 9 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 360 3 0 4 4.4 COc1cc(Br)c(-n2ccc3c(C)cc(C)nc32)c(OC)c1 10.1021/jm980223o
9884878 173025 18 None - 1 Human 9.0 pKi = 9 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptorsCompound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm990590f
CHEMBL45187 173025 18 None - 1 Human 9.0 pKi = 9 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptorsCompound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1021/jm990590f
9884878 173025 18 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptorDisplacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptor
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.ejmech.2016.11.019
CHEMBL45187 173025 18 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptorDisplacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptor
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.ejmech.2016.11.019
10428930 203687 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 365 6 0 5 4.9 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)nn(C)c12 10.1016/s0960-894x(02)00358-x
CHEMBL67484 203687 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 365 6 0 5 4.9 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)nn(C)c12 10.1016/s0960-894x(02)00358-x
9822241 64009 8 None 9 2 Human 9.0 pKi = 9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 8 1 6 5.0 CCC(CC)Nc1nc(C)c(-c2ccc(OC(F)(F)F)cc2OC)nc1OC 10.1021/jm200365y
CHEMBL1807053 64009 8 None 9 2 Human 9.0 pKi = 9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 8 1 6 5.0 CCC(CC)Nc1nc(C)c(-c2ccc(OC(F)(F)F)cc2OC)nc1OC 10.1021/jm200365y
9884878 173025 18 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmc.2011.07.055
CHEMBL45187 173025 18 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma countingDisplacement of [125I]CRF from human corticotropin-releasing factor receptor 1 expressed in CHO-K1 cells after 2 hrs by gamma counting
ChEMBL 352 6 1 5 4.9 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmc.2011.07.055
CHEMBL2373995 210382 0 None 1 2 Human 9.0 pKi = 9.0 Binding
Binding affinity of the receptor corticotropin releasing factor receptor with peptidic agonistsBinding affinity of the receptor corticotropin releasing factor receptor with peptidic agonists
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCCN1C(=O)N[C@@H](CC(=O)O)C(=O)[C@H](CC(=O)O)NC(=O)[C@@H](N)CC(N)=O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(N)=O)C(C)C 10.1021/jm990590f
CHEMBL4299314 213566 0 None -1 2 Human 9.0 pKi = 9.0 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@H](CC(N)=O)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C(N)=O)[C@H](C)CC)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
9913240 67947 0 None - 1 Human 9.0 pKi = 9.0 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 484 7 0 5 6.2 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(C(C)C)cc3Br)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL191090 67947 0 None - 1 Human 9.0 pKi = 9.0 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 484 7 0 5 6.2 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(C(C)C)cc3Br)c3nc(C)cc1c32 10.1021/jm050384+
44392663 65521 0 None - 1 Human 9.0 pKi = 9.0 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 453 8 0 5 6.5 CCCCN(CCCC)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL183068 65521 0 None - 1 Human 9.0 pKi = 9.0 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 453 8 0 5 6.5 CCCCN(CCCC)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
44290322 101170 0 None - 1 Human 9.0 pKi = 9.0 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 382 8 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL295563 101170 0 None - 1 Human 9.0 pKi = 9.0 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 382 8 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
23595022 64014 0 None - 1 Human 9.0 pKi = 9.0 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 363 8 1 5 5.0 CCc1nc(-c2ccc(OC)cc2Cl)c(OC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1807058 64014 0 None - 1 Human 9.0 pKi = 9.0 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 363 8 1 5 5.0 CCc1nc(-c2ccc(OC)cc2Cl)c(OC)nc1NC(CC)CC 10.1021/jm200365y
10667354 116600 0 None - 1 Human 9.0 pKi = 9.0 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 377 5 1 5 5.3 CCC(CC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL336678 116600 0 None - 1 Human 9.0 pKi = 9.0 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 377 5 1 5 5.3 CCC(CC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL4299294 213561 0 None -3 2 Human 9.0 pKi = 9.0 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@H](C)C(=O)N[C@H](CCC(=O)O)C(=O)N[C@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@H](C)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@@H]1CCC(=O)NCCCC[C@H](C(=O)N[C@H](CC(N)=O)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CC(C)C)C(=O)NC(CC2CCCCC2)C(=O)N[C@H](CC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C(N)=O)[C@H](C)CC)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@H](C)NC1=O 10.1021/acs.jmedchem.5b00926
CHEMBL4299355 213574 0 None -1 2 Human 8.9 pKi = 8.9 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)N(C)[C@@H](C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
44392722 64566 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 439 7 0 5 6.1 CCCCN(CCC)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL181536 64566 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 439 7 0 5 6.1 CCCCN(CCC)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
44392695 123872 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 425 6 0 5 5.7 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL362697 123872 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 425 6 0 5 5.7 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
44341892 110320 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 418 8 0 4 6.7 CCCCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL323886 110320 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 418 8 0 4 6.7 CCCCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
10668220 31278 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 391 6 1 5 5.7 CCCC(CC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL140143 31278 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 391 6 1 5 5.7 CCCC(CC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
10832574 116789 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 363 4 0 5 4.6 CCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL337768 116789 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 363 4 0 5 4.6 CCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
44347200 161741 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 382 8 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)c(OC)c3)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL413756 161741 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 382 8 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)c(OC)c3)c(C)nn12 10.1016/j.bmcl.2004.05.019
11774042 203352 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL65078 203352 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.019
44341936 9616 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 404 7 0 4 6.3 CCCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112626 9616 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 404 7 0 4 6.3 CCCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
44341723 168133 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 416 7 0 4 6.3 CCCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL432976 168133 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 416 7 0 4 6.3 CCCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
18629227 101487 0 None - 1 Human 8.9 pKi = 8.9 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.
ChEMBL 389 4 0 5 5.5 CCC(CC)n1nnc2c(N3CCc4cc(Cl)cc(Cl)c43)nc(C)cc21 10.1021/jm990590f
CHEMBL297868 101487 0 None - 1 Human 8.9 pKi = 8.9 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.
ChEMBL 389 4 0 5 5.5 CCC(CC)n1nnc2c(N3CCc4cc(Cl)cc(Cl)c43)nc(C)cc21 10.1021/jm990590f
90231873 123950 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 494 6 1 4 5.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Br)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628728 123950 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 494 6 1 4 5.6 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Br)cc1Br 10.1016/j.bmcl.2015.10.010
23595046 64010 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 383 7 1 5 5.1 CCC(CC)Nc1nc(C)c(-c2ccc(C(F)(F)F)cc2OC)nc1OC 10.1021/jm200365y
CHEMBL1807054 64010 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 383 7 1 5 5.1 CCC(CC)Nc1nc(C)c(-c2ccc(C(F)(F)F)cc2OC)nc1OC 10.1021/jm200365y
11236249 126199 0 None - 1 Human 8.9 pKi = 8.9 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 448 6 0 6 5.5 CCN(Cc1ccc(Cl)cc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL364987 126199 0 None - 1 Human 8.9 pKi = 8.9 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 448 6 0 6 5.5 CCN(Cc1ccc(Cl)cc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
10648981 120742 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 497 7 0 5 6.7 CCCCN(CC)c1nc(C)nc2c1nc(C(F)(F)F)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL354982 120742 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 497 7 0 5 6.7 CCCCN(CC)c1nc(C)nc2c1nc(C(F)(F)F)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341845 9498 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 436 8 0 5 6.2 CCCCN(CCSC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112057 9498 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 436 8 0 5 6.2 CCCCN(CCSC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
22248935 64008 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 9 1 5 5.6 CCc1nc(NC(CC)CC)c(OC)nc1-c1ccc(OC(F)F)cc1Cl 10.1021/jm200365y
CHEMBL1807052 64008 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 9 1 5 5.6 CCc1nc(NC(CC)CC)c(OC)nc1-c1ccc(OC(F)F)cc1Cl 10.1021/jm200365y
10479355 129479 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 459 8 0 6 5.6 CCCCN(CC)c1nc(C)nc2c1nc(OC)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL367253 129479 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 459 8 0 6 5.6 CCCCN(CC)c1nc(C)nc2c1nc(OC)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
44386320 131344 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 463 7 0 5 6.3 CCCCN(CC)c1nc(C)nc2c1nc(Cl)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL368772 131344 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 463 7 0 5 6.3 CCCCN(CC)c1nc(C)nc2c1nc(Cl)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
10813254 120761 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 445 8 0 6 5.8 CCCCC(CC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL355214 120761 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 445 8 0 6 5.8 CCCCC(CC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341735 110921 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 430 8 0 4 6.7 CCCCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL326156 110921 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 430 8 0 4 6.7 CCCCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
15486940 159801 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptorDisplacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptor
ChEMBL 356 5 1 4 5.6 CCC(CC)Nc1cc(C)nc2c(-c3ccc(C)cc3Cl)c(C)nn12 10.1016/j.ejmech.2016.11.019
CHEMBL4105538 159801 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptorDisplacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptor
ChEMBL 356 5 1 4 5.6 CCC(CC)Nc1cc(C)nc2c(-c3ccc(C)cc3Cl)c(C)nn12 10.1016/j.ejmech.2016.11.019
9952997 170603 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1021/jm049085v
CHEMBL445075 170603 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1021/jm049085v
11462455 114772 2 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 356 6 0 4 5.3 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL333903 114772 2 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 356 6 0 4 5.3 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
3495 1175 28 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm9904351
5311055 1175 28 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm9904351
CHEMBL9946 1175 28 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm9904351
10136000 29139 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 405 7 1 5 6.1 CCCC(CCC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL138154 29139 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 405 7 1 5 6.1 CCCC(CCC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
10692703 32373 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 405 7 1 5 6.1 CCCCC(CC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL141085 32373 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 405 7 1 5 6.1 CCCCC(CC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
11774042 203352 0 None - 1 Human 8.8 pKi = 8.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm040058e
CHEMBL65078 203352 0 None - 1 Human 8.8 pKi = 8.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm040058e
3495 1175 28 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm980224g
5311055 1175 28 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm980224g
CHEMBL9946 1175 28 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm980224g
44392653 123231 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 473 6 0 5 6.5 CCCN(Cc1ccccc1)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL361314 123231 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 473 6 0 5 6.5 CCCN(Cc1ccccc1)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
9951076 67411 2 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1016/j.bmcl.2012.08.112
CHEMBL188844 67411 2 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1016/j.bmcl.2012.08.112
CHEMBL2165204 67411 2 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1016/j.bmcl.2012.08.112
10291750 84613 26 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 355 7 1 7 3.8 CCC(COC)n1nnc2c(Nc3ccc(OC)cc3C)nc(C)cc21 10.1016/j.bmcl.2012.08.112
CHEMBL2165203 84613 26 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 355 7 1 7 3.8 CCC(COC)n1nnc2c(Nc3ccc(OC)cc3C)nc(C)cc21 10.1016/j.bmcl.2012.08.112
CHEMBL2221285 84613 26 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 355 7 1 7 3.8 CCC(COC)n1nnc2c(Nc3ccc(OC)cc3C)nc(C)cc21 10.1016/j.bmcl.2012.08.112
78075688 84614 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 436 9 0 6 4.4 COCCN(CCOC)Cc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2012.08.112
CHEMBL2165205 84614 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 436 9 0 6 4.4 COCCN(CCOC)Cc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2012.08.112
CHEMBL2221286 84614 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 436 9 0 6 4.4 COCCN(CCOC)Cc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2012.08.112
3499 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to human CRF1 receptor assessed as inhibition constantBinding affinity to human CRF1 receptor assessed as inhibition constant
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.ejmech.2021.113537
9909468 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to human CRF1 receptor assessed as inhibition constantBinding affinity to human CRF1 receptor assessed as inhibition constant
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.ejmech.2021.113537
CHEMBL44698 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to human CRF1 receptor assessed as inhibition constantBinding affinity to human CRF1 receptor assessed as inhibition constant
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1016/j.ejmech.2021.113537
9931767 9516 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 416 7 0 4 6.4 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(CC)c12 10.1016/s0960-894x(03)00621-8
CHEMBL112152 9516 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 416 7 0 4 6.4 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(CC)c12 10.1016/s0960-894x(03)00621-8
9952997 170603 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
CHEMBL445075 170603 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
9952997 170603 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL445075 170603 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
3499 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
9909468 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
CHEMBL44698 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
137645497 157634 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptorDisplacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptor
ChEMBL 356 5 1 4 5.6 CCC(CC)Nc1cc(C)nc2c(-c3ccc(Cl)cc3C)c(C)nn12 10.1016/j.ejmech.2016.11.019
CHEMBL4081285 157634 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptorDisplacement of [125I-Tyr0]-CRF from recombinant human CRF1 receptor
ChEMBL 356 5 1 4 5.6 CCC(CC)Nc1cc(C)nc2c(-c3ccc(Cl)cc3C)c(C)nn12 10.1016/j.ejmech.2016.11.019
3499 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm9904351
9909468 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm9904351
CHEMBL44698 1448 28 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm9904351
176157 2738 28 None 9 2 Human 8.8 pKi = 8.8 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm960149e
3512 2738 28 None 9 2 Human 8.8 pKi = 8.8 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm960149e
CHEMBL45281 2738 28 None 9 2 Human 8.8 pKi = 8.8 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm960149e
176157 2738 28 None 9 2 Human 8.8 pKi = 8.8 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm9900117
3512 2738 28 None 9 2 Human 8.8 pKi = 8.8 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm9900117
CHEMBL45281 2738 28 None 9 2 Human 8.8 pKi = 8.8 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm9900117
3499 1448 28 None - 1 Human 8.7 pKi = 8.7 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
9909468 1448 28 None - 1 Human 8.7 pKi = 8.7 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
CHEMBL44698 1448 28 None - 1 Human 8.7 pKi = 8.7 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10.1021/jm990590f
10224173 32371 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 423 8 0 7 3.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL141084 32371 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 423 8 0 7 3.8 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
10344587 167844 0 None 1 2 Rat 8.7 pKi = 8.7 Binding
Affinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brainAffinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brain
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1021/jm034077k
CHEMBL1762817 167844 0 None 1 2 Rat 8.7 pKi = 8.7 Binding
Affinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brainAffinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brain
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1021/jm034077k
CHEMBL430892 167844 0 None 1 2 Rat 8.7 pKi = 8.7 Binding
Affinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brainAffinity for the Corticotropin releasing factor receptor 1 (CRHR1) was determined in rat brain
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1021/jm034077k
9824227 58951 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 433 7 0 7 4.2 CCC(COC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168936 58951 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 433 7 0 7 4.2 CCC(COC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
9931814 59018 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 417 6 0 6 5.0 CCC(CC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169248 59018 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 417 6 0 6 5.0 CCC(CC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44347138 15271 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 382 8 0 6 4.7 CCCCN(CC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL121286 15271 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 382 8 0 6 4.7 CCCCN(CC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
23595043 64005 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 357 9 1 5 4.9 CCc1cc(OC)ccc1-c1nc(OC)c(NC(CC)CC)nc1CC 10.1021/jm200365y
CHEMBL1807049 64005 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 357 9 1 5 4.9 CCc1cc(OC)ccc1-c1nc(OC)c(NC(CC)CC)nc1CC 10.1021/jm200365y
10786785 29140 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 393 6 1 6 4.6 CCC(COC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL138155 29140 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 393 6 1 6 4.6 CCC(COC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
11639435 71571 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 376 5 0 5 4.7 CC[C@H]1Cn2nc(-c3ccc(OC)cc3C)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL196312 71571 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 376 5 0 5 4.7 CC[C@H]1Cn2nc(-c3ccc(OC)cc3C)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11575986 124368 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 448 4 0 4 6.7 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3C[C@H](c1ccccc1)N2CC1CC1 10.1021/jm049085v
CHEMBL363779 124368 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 448 4 0 4 6.7 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3C[C@H](c1ccccc1)N2CC1CC1 10.1021/jm049085v
10740981 57836 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 423 8 0 7 4.0 CCN(CC)c1nc(C)nc(N(CC)c2c(Br)cc(OC)cc2OC)n1 10.1021/jm980222w
CHEMBL167122 57836 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 423 8 0 7 4.0 CCN(CC)c1nc(C)nc(N(CC)c2c(Br)cc(OC)cc2OC)n1 10.1021/jm980222w
10595854 120259 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 378 8 0 6 4.5 CCN(CC)c1cc(C)nc(N(CC)c2c(Cl)cc(OC)cc2OC)n1 10.1021/jm980222w
CHEMBL352378 120259 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 378 8 0 6 4.5 CCN(CC)c1cc(C)nc(N(CC)c2c(Cl)cc(OC)cc2OC)n1 10.1021/jm980222w
44392741 65240 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 367 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL182700 65240 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 367 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
11164902 66302 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(C)C)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL184850 66302 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(C)C)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
44375351 56518 0 None - 1 Rat 8.0 pKi = 8 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 424 9 0 4 6.6 CCCCN(CCCCF)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(00)00071-8
CHEMBL163618 56518 0 None - 1 Rat 8.0 pKi = 8 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 424 9 0 4 6.6 CCCCN(CCCCF)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(00)00071-8
44307737 100852 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 383 8 0 7 4.0 CCCN(CCC)c1nc(C)nc2c(-c3ccc(OC)cc3OC)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL293469 100852 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 383 8 0 7 4.0 CCCN(CCC)c1nc(C)nc2c(-c3ccc(OC)cc3OC)n(C)nc12 10.1016/s0960-894x(02)00358-x
11164902 66302 0 None - 1 Human 8.0 pKi = 8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL184850 66302 0 None - 1 Human 8.0 pKi = 8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
44337527 7448 0 None - 1 Human 8.0 pKi = 8 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 402 7 0 4 5.0 CCCN(c1nc(-c2ccc(Br)cc2C)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL108673 7448 0 None - 1 Human 8.0 pKi = 8 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 402 7 0 4 5.0 CCCN(c1nc(-c2ccc(Br)cc2C)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
44266482 4499 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 5 0 3 7.8 CCN(c1nc(C)cc(-c2c(Cl)cccc2Cl)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10208 4499 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 5 0 3 7.8 CCN(c1nc(C)cc(-c2c(Cl)cccc2Cl)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
10813394 59171 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 448 8 1 8 3.5 COCC(COC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169998 59171 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 448 8 1 8 3.5 COCC(COC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341818 110495 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 420 8 0 5 5.5 CCCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL324889 110495 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 420 8 0 5 5.5 CCCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9867507 59067 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 0 7 3.9 CCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169539 59067 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 0 7 3.9 CCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10576086 59101 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 463 9 0 9 2.4 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(N(C)C)cc1Br 10.1021/jm980224g
CHEMBL169711 59101 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 463 9 0 9 2.4 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(N(C)C)cc1Br 10.1021/jm980224g
44341817 172575 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 420 7 0 5 5.4 COCCN(CC(C)C)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL448788 172575 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 420 7 0 5 5.4 COCCN(CC(C)C)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
10574875 120744 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 434 7 0 7 4.6 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(SC)cc1Br 10.1021/jm980224g
CHEMBL355006 120744 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 434 7 0 7 4.6 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(SC)cc1Br 10.1021/jm980224g
12967651 19919 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 445 8 0 4 6.8 CCCN(Cc1sc(N(C)c2c(C)cc(C)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL130264 19919 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 445 8 0 4 6.8 CCCN(Cc1sc(N(C)c2c(C)cc(C)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
44392710 64600 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 366 7 0 7 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N=O)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL181684 64600 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 366 7 0 7 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N=O)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
10671924 59376 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 466 7 0 8 3.3 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(S(C)(=O)=O)cc1Br 10.1021/jm980224g
CHEMBL170844 59376 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 466 7 0 8 3.3 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(S(C)(=O)=O)cc1Br 10.1021/jm980224g
44347108 15246 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 370 7 0 4 5.5 CCCN(CCC)c1cc(CC)nc2c(-c3ccc(Cl)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL121116 15246 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 370 7 0 4 5.5 CCCN(CCC)c1cc(CC)nc2c(-c3ccc(Cl)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
44305971 100604 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 395 10 0 6 4.4 C=CCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL291828 100604 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 395 10 0 6 4.4 C=CCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
20780034 130468 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 382 7 0 4 4.8 CCCN(CCC)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL368041 130468 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 382 7 0 4 4.8 CCCN(CCC)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
10298157 123233 0 None - 1 Human 7.0 pKi = 7 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 457 8 1 4 7.3 C=CCN(CCC)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL361323 123233 0 None - 1 Human 7.0 pKi = 7 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 457 8 1 4 7.3 C=CCN(CCC)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
10207702 131991 0 None - 1 Human 7.0 pKi = 7 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 508 8 1 5 7.7 CCCN(Cc1ccncc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL369531 131991 0 None - 1 Human 7.0 pKi = 7 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 508 8 1 5 7.7 CCCN(Cc1ccncc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
11246476 124055 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 396 6 0 7 3.4 CCCC(OC)N1CCn2c(=O)n(-c3ccc(OC)cc3C)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL363152 124055 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 396 6 0 7 3.4 CCCC(OC)N1CCn2c(=O)n(-c3ccc(OC)cc3C)c3nc(C)cc1c32 10.1021/jm050384+
44389125 64617 0 None - 1 Human 5.0 pKi = 5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 429 4 1 4 6.5 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN1CCCC1 10.1016/j.bmcl.2004.10.055
CHEMBL181765 64617 0 None - 1 Human 5.0 pKi = 5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 429 4 1 4 6.5 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN1CCCC1 10.1016/j.bmcl.2004.10.055
44460545 205567 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 452 7 1 3 6.8 O=C(CCc1ccncc1)C(Nc1ccc(Cl)cc1Cl)c1ccccc1C(F)(F)F 10.1021/jm049974i
CHEMBL81262 205567 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 452 7 1 3 6.8 O=C(CCc1ccncc1)C(Nc1ccc(Cl)cc1Cl)c1ccccc1C(F)(F)F 10.1021/jm049974i
10790231 59038 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 462 10 0 10 2.1 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1S(C)(=O)=O 10.1021/jm980224g
CHEMBL169365 59038 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 462 10 0 10 2.1 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1S(C)(=O)=O 10.1021/jm980224g
44446715 94741 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1c(C)nc(-c2ccc(Cl)cc2Cl)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253084 94741 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 386 6 0 2 7.1 CCCN(CCC)c1c(C)nc(-c2ccc(Cl)cc2Cl)c2ccccc12 10.1016/j.bmcl.2007.12.050
44460553 205896 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity of compound towards human Corticotropin releasing factor receptor 1Binding affinity of compound towards human Corticotropin releasing factor receptor 1
ChEMBL 442 7 1 3 6.2 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2Br)c(Cl)c1 10.1021/jm049974i
CHEMBL83914 205896 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity of compound towards human Corticotropin releasing factor receptor 1Binding affinity of compound towards human Corticotropin releasing factor receptor 1
ChEMBL 442 7 1 3 6.2 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2Br)c(Cl)c1 10.1021/jm049974i
10548395 102860 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 389 8 1 5 5.7 CCCCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
CHEMBL305671 102860 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 389 8 1 5 5.7 CCCCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
10542924 205138 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 309 3 1 5 3.6 Cc1cc(C)c(Nc2nc(C)nc(N3CC=CCC3)n2)c(C)c1 10.1021/jm960148m
CHEMBL78035 205138 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 309 3 1 5 3.6 Cc1cc(C)c(Nc2nc(C)nc(N3CC=CCC3)n2)c(C)c1 10.1021/jm960148m
10548395 102860 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 389 8 1 5 5.7 CCCCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
CHEMBL305671 102860 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 389 8 1 5 5.7 CCCCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
10542924 205138 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 309 3 1 5 3.6 Cc1cc(C)c(Nc2nc(C)nc(N3CC=CCC3)n2)c(C)c1 10.1021/jm9900117
CHEMBL78035 205138 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 309 3 1 5 3.6 Cc1cc(C)c(Nc2nc(C)nc(N3CC=CCC3)n2)c(C)c1 10.1021/jm9900117
44446735 94629 0 None - 1 Human 6.0 pKi = 6.0 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 428 8 0 5 5.9 CCCN(CCn1ccnc1)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL252301 94629 0 None - 1 Human 6.0 pKi = 6.0 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 428 8 0 5 5.9 CCCN(CCn1ccnc1)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
44460602 205746 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 459 6 2 4 6.2 COc1ccc(C(=O)C(Nc2ccc(C)cc2Cl)c2ccccc2Br)cc1O 10.1021/jm049974i
CHEMBL82707 205746 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 459 6 2 4 6.2 COc1ccc(C(=O)C(Nc2ccc(C)cc2Cl)c2ccccc2Br)cc1O 10.1021/jm049974i
44317955 103920 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 470 6 2 3 5.8 CNC(=O)c1cccc(C(=O)C(Nc2ccc(C)cc2Cl)c2ccccc2Br)c1 10.1021/jm049974i
CHEMBL309244 103920 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 470 6 2 3 5.8 CNC(=O)c1cccc(C(=O)C(Nc2ccc(C)cc2Cl)c2ccccc2Br)c1 10.1021/jm049974i
11395370 74178 0 None - 1 Rat 6.0 pKi = 6.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 396 5 2 5 4.4 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(CO)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL202299 74178 0 None - 1 Rat 6.0 pKi = 6.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 396 5 2 5 4.4 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(CO)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
11065773 202995 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 278 4 2 4 2.8 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1C#N 10.1021/jm025512y
CHEMBL63140 202995 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 278 4 2 4 2.8 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1C#N 10.1021/jm025512y
44266473 4418 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 409 5 0 3 6.5 CCN(c1nc(C)cc(-c2ccccc2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10150 4418 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 409 5 0 3 6.5 CCN(c1nc(C)cc(-c2ccccc2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
10494830 120348 1 None - 1 Rat 6.0 pKi = 6.0 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 305 2 0 3 3.9 Cc1ccc(N(C)c2nc(C)cc(C)n2)c(Br)c1 10.1021/jm980222w
CHEMBL353075 120348 1 None - 1 Rat 6.0 pKi = 6.0 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 305 2 0 3 3.9 Cc1ccc(N(C)c2nc(C)cc(C)n2)c(Br)c1 10.1021/jm980222w
20780064 124329 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 480 7 0 4 6.8 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CC4CC4)CC4CC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL363592 124329 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 480 7 0 4 6.8 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CC4CC4)CC4CC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
11797750 58096 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 448 10 0 5 5.7 CCCN(CCOC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL167444 58096 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 448 10 0 5 5.7 CCCN(CCOC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10739468 59005 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 395 7 0 5 4.9 CCN(CC)c1cc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
CHEMBL169094 59005 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 395 7 0 5 4.9 CCN(CC)c1cc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
44347356 112869 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 372 7 1 5 4.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)c(CO)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL330954 112869 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 372 7 1 5 4.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)c(CO)nn12 10.1016/j.bmcl.2004.05.019
44341712 114960 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL334262 114960 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
10024020 203102 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 401 9 0 5 5.2 CCCN(c1nccc(-c2c(Cl)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL63989 203102 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 401 9 0 5 5.2 CCCN(c1nccc(-c2c(Cl)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
44307806 203772 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 393 8 0 5 5.8 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)n(CCC)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL68076 203772 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 393 8 0 5 5.8 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)n(CCC)nc12 10.1016/s0960-894x(02)00358-x
44305523 102168 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 392 6 0 5 4.8 CCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL302645 102168 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 392 6 0 5 4.8 CCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
20780164 93721 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 421 7 0 5 5.7 C=CCN(CCC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL247151 93721 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 421 7 0 5 5.7 C=CCN(CCC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
20780148 151123 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 435 7 0 5 5.9 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
CHEMBL395929 151123 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 435 7 0 5 5.9 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
9980466 154128 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 436 9 1 6 5.2 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1016/j.bmcl.2007.09.008
CHEMBL398531 154128 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 436 9 1 6 5.2 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1016/j.bmcl.2007.09.008
10302495 123289 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 541 8 1 4 8.9 CCCN(Cc1ccc(Cl)cc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL361438 123289 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 541 8 1 4 8.9 CCCN(Cc1ccc(Cl)cc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
11189570 127483 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 6 0 6 5.2 Cc1cc(N(Cc2ccccc2)C(C)C)n2nc(C)c(-c3cnc(N(C)C)cc3C)c2n1 10.1021/jm040058e
CHEMBL366096 127483 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 6 0 6 5.2 Cc1cc(N(Cc2ccccc2)C(C)C)n2nc(C)c(-c3cnc(N(C)C)cc3C)c2n1 10.1021/jm040058e
9803645 58723 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 446 7 0 7 4.3 CCC(COC)N(C)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168519 58723 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 446 7 0 7 4.3 CCC(COC)N(C)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341858 111134 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 446 7 0 5 6.0 CCCCN(CC1CCCO1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL326355 111134 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 446 7 0 5 6.0 CCCCN(CC1CCCO1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
18691306 98576 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 451 5 0 3 7.4 CCN(c1nc(C)cc(-c2c(C)cc(C)cc2C)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL276716 98576 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 451 5 0 3 7.4 CCN(c1nc(C)cc(-c2c(C)cc(C)cc2C)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
22249041 63977 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 358 9 1 6 4.3 CCc1nc(-c2ccc(OC)nc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806958 63977 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 358 9 1 6 4.3 CCc1nc(-c2ccc(OC)nc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
11155051 106350 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 446 8 0 5 6.2 CCCN(c1nc(-c2ccc(OC)cc2C)n(C)n1)[C@@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
CHEMBL3085415 106350 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 446 8 0 5 6.2 CCCN(c1nc(-c2ccc(OC)cc2C)n(C)n1)[C@@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
CHEMBL3139200 106350 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 446 8 0 5 6.2 CCCN(c1nc(-c2ccc(OC)cc2C)n(C)n1)[C@@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
136216703 78905 0 None -5 5 Rat 7.0 pKi = 7.0 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 482 2 4 7 4.0 N[C@H]1CCCC[C@@H]1NC(=O)c1c2c(c3c4c(ncnc14)-c1ccccc1C3=O)N[C@@H]1CCCC[C@H]1N2 10.1016/s0960-894x(99)00075-x
CHEMBL2112936 78905 0 None -5 5 Rat 7.0 pKi = 7.0 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 482 2 4 7 4.0 N[C@H]1CCCC[C@@H]1NC(=O)c1c2c(c3c4c(ncnc14)-c1ccccc1C3=O)N[C@@H]1CCCC[C@H]1N2 10.1016/s0960-894x(99)00075-x
44392740 123826 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 337 6 0 5 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncccc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL362437 123826 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 337 6 0 5 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncccc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
10142769 6502 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 520 8 0 4 7.3 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC4CC4)CCC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082720 6502 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 520 8 0 4 7.3 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC4CC4)CCC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
44392771 66671 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 399 10 0 7 3.7 CCCN(CC1CC1)c1cc(C(=O)c2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL185400 66671 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 399 10 0 7 3.7 CCCN(CC1CC1)c1cc(C(=O)c2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
44389050 62502 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 505 6 2 8 7.1 CSc1snnc1NCc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL178131 62502 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 505 6 2 8 7.1 CSc1snnc1NCc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
10140223 123255 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 471 8 1 4 7.5 CCN(CCC1CC1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL361394 123255 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 471 8 1 4 7.5 CCN(CCC1CC1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
10160871 19812 0 None - 1 Human 5.0 pKi = 5.0 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 445 8 1 4 6.7 CCCN(CC1CC1)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1CC 10.1016/j.bmcl.2003.08.055
CHEMBL130180 19812 0 None - 1 Human 5.0 pKi = 5.0 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 445 8 1 4 6.7 CCCN(CC1CC1)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1CC 10.1016/j.bmcl.2003.08.055
10551027 57589 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 438 3 0 5 4.9 Cc1cc(N2CCOCC2)c2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL166760 57589 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 438 3 0 5 4.9 Cc1cc(N2CCOCC2)c2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
44307652 203798 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 391 7 1 5 5.6 CCCCCCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL68303 203798 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 391 7 1 5 5.6 CCCCCCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
44385525 60040 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 394 6 0 7 3.4 CCCN(CC1CC1)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)nc1C 10.1016/s0960-894x(99)00108-0
CHEMBL173624 60040 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 394 6 0 7 3.4 CCCN(CC1CC1)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)nc1C 10.1016/s0960-894x(99)00108-0
10902707 203598 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 301 4 2 3 3.9 CC(=O)/C(=N\c1cccc(C)c1)NNc1ccccc1Cl 10.1021/jm025512y
CHEMBL66950 203598 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 301 4 2 3 3.9 CC(=O)/C(=N\c1cccc(C)c1)NNc1ccccc1Cl 10.1021/jm025512y
44308155 203715 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 446 7 0 6 5.0 CCCN(CCN1CCCC1)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL67646 203715 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 446 7 0 6 5.0 CCCN(CCN1CCCC1)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
44443574 94331 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 381 8 2 5 5.6 CCc1nc(NC(CC)CC)c(CC)nc1Nc1ncc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.008
CHEMBL250616 94331 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 381 8 2 5 5.6 CCc1nc(NC(CC)CC)c(CC)nc1Nc1ncc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.008
10567951 205078 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 323 7 1 5 4.0 C=CCN(CC=C)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
CHEMBL77391 205078 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 323 7 1 5 4.0 C=CCN(CC=C)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
10567951 205078 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 323 7 1 5 4.0 C=CCN(CC=C)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
CHEMBL77391 205078 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 323 7 1 5 4.0 C=CCN(CC=C)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
10222698 187850 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 401 10 1 6 4.3 CCCN(CCC)c1c(CC(C)O)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL496269 187850 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 401 10 1 6 4.3 CCCN(CCC)c1c(CC(C)O)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
44385545 60277 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 499 9 0 6 5.8 CCCCN(CC)c1nc(C)nc2c1n(CC1CC1)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL174213 60277 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 499 9 0 6 5.8 CCCCN(CC)c1nc(C)nc2c1n(CC1CC1)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
44385463 61379 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 433 6 1 7 3.4 COCCNc1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL176937 61379 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 433 6 1 7 3.4 COCCNc1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
20780127 135242 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 446 6 0 4 5.9 CCCN(CC1CC1)C(=O)c1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ccc(F)cc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL372499 135242 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 446 6 0 4 5.9 CCCN(CC1CC1)C(=O)c1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ccc(F)cc3n12 10.1016/j.bmcl.2005.06.028
135593026 63947 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 343 8 2 5 4.6 CCc1nc(-c2ccc(OC)cc2O)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806735 63947 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 343 8 2 5 4.6 CCc1nc(-c2ccc(OC)cc2O)c(CC)nc1NC(CC)CC 10.1021/jm200365y
44443571 94330 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 314 7 0 5 4.2 CCCN(CCC)c1nc(C)c(Oc2cc(C)ccn2)nc1C 10.1016/j.bmcl.2007.09.008
CHEMBL250615 94330 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 314 7 0 5 4.2 CCCN(CCC)c1nc(C)c(Oc2cc(C)ccn2)nc1C 10.1016/j.bmcl.2007.09.008
11475729 75376 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 422 7 1 5 5.5 C=CCOc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
CHEMBL203807 75376 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 422 7 1 5 5.5 C=CCOc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
9887145 126651 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 398 6 0 5 4.9 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(Cl)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL365260 126651 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 398 6 0 5 4.9 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(Cl)cc3)c3nc(C)cc1c32 10.1021/jm050384+
9907170 178099 0 None -2 2 Human 7.9 pKi = 7.9 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 365 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980222w
CHEMBL46479 178099 0 None -2 2 Human 7.9 pKi = 7.9 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 365 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980222w
44392687 66668 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 457 8 0 7 4.2 COCCN(CCOC)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL185393 66668 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 457 8 0 7 4.2 COCCN(CCOC)c1cc(C)nc2c(-c3ncc(C(F)(F)F)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
21916254 6405 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 576 7 0 4 8.3 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)Cc4ccc(Cl)cc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082338 6405 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 576 7 0 4 8.3 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)Cc4ccc(Cl)cc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
10300313 6819 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 494 7 0 4 6.9 CCCN(CCC(F)(F)F)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1083935 6819 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 494 7 0 4 6.9 CCCN(CCC(F)(F)F)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
22248932 63994 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 463 6 1 3 6.2 CCc1nc(NC(CC)CC)c(I)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
CHEMBL1807034 63994 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 463 6 1 3 6.2 CCc1nc(NC(CC)CC)c(I)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
44388407 63011 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 466 8 0 5 6.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
CHEMBL178735 63011 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 466 8 0 5 6.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
9907170 178099 0 None -2 2 Human 7.9 pKi = 7.9 Binding
Inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneInhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 365 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm990590f
CHEMBL46479 178099 0 None -2 2 Human 7.9 pKi = 7.9 Binding
Inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneInhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 365 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm990590f
44341663 110874 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 432 8 0 4 5.9 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)ccc12 10.1016/s0960-894x(03)00684-x
CHEMBL326107 110874 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 432 8 0 4 5.9 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)ccc12 10.1016/s0960-894x(03)00684-x
44384779 59711 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 487 8 0 7 4.2 COCCN(CC1CC1)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL172358 59711 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 487 8 0 7 4.2 COCCN(CC1CC1)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
10739849 58503 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 401 5 0 5 4.9 CCN(CC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168353 58503 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 401 5 0 5 4.9 CCN(CC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341762 10155 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 406 7 0 5 5.1 CCN(CCCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL115820 10155 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 406 7 0 5 5.1 CCN(CCCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
11625175 71912 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 384 4 0 4 5.2 CC[C@H]1Cn2nc(-c3ccc(F)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL197187 71912 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 384 4 0 4 5.2 CC[C@H]1Cn2nc(-c3ccc(F)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11530590 140776 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 360 4 0 4 5.0 CC[C@H]1Cn2nc(-c3ccc(C)cc3C)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL381850 140776 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 360 4 0 4 5.0 CC[C@H]1Cn2nc(-c3ccc(C)cc3C)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
9957261 65276 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 490 7 0 6 7.0 CCCN(CC1CC1)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
CHEMBL18285 65276 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 490 7 0 6 7.0 CCCN(CC1CC1)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
10669526 165414 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 414 4 1 6 4.8 Cc1nc(NC2CCCC2)c2nnn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980224g
CHEMBL423833 165414 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 414 4 1 6 4.8 Cc1nc(NC2CCCC2)c2nnn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980224g
44446738 94648 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 473 10 0 4 7.3 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCCCC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL252492 94648 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 473 10 0 4 7.3 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCCCC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
10117501 64185 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 493 7 1 4 7.9 CCN(Cc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL180880 64185 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 493 7 1 4 7.9 CCN(Cc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
11441193 63416 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 408 10 0 6 5.3 CCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL179647 63416 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 408 10 0 6 5.3 CCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2OC)n(C)n1 10.1021/jm049339c
44337549 9174 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 352 7 0 4 4.8 CCCN(c1nc(-c2c(C)cc(C)cc2C)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL110222 9174 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 352 7 0 4 4.8 CCCN(c1nc(-c2c(C)cc(C)cc2C)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
11223627 68671 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 410 6 0 6 3.9 COCC(COC)N1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL192082 68671 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 410 6 0 6 3.9 COCC(COC)N1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
44392731 123752 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 385 9 0 6 3.3 COCCN(CCOC)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL362226 123752 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 385 9 0 6 3.3 COCCN(CCOC)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
46891008 6434 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 424 3 0 4 5.7 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCCCC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082441 6434 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 424 3 0 4 5.7 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCCCC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
20780056 146241 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 444 5 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)Cc4ccncc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL392044 146241 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 444 5 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)Cc4ccncc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
20780286 7329 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 448 6 0 4 5.6 CCCN(CC1CC1)C(=O)c1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
CHEMBL1086164 7329 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 448 6 0 4 5.6 CCCN(CC1CC1)C(=O)c1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
44389097 63015 0 None - 1 Human 4.9 pKi = 4.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 441 4 1 4 6.6 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN1CC=CCC1 10.1016/j.bmcl.2004.10.055
CHEMBL178751 63015 0 None - 1 Human 4.9 pKi = 4.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 441 4 1 4 6.6 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN1CC=CCC1 10.1016/j.bmcl.2004.10.055
10853581 120264 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 326 5 1 7 2.5 COCCNc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL352436 120264 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 326 5 1 7 2.5 COCCNc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
44443572 154774 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 326 7 0 5 4.2 CCCN(CC1CC1)c1nc(C)c(Oc2cc(C)ccn2)nc1C 10.1016/j.bmcl.2007.09.008
CHEMBL400155 154774 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 326 7 0 5 4.2 CCCN(CC1CC1)c1nc(C)c(Oc2cc(C)ccn2)nc1C 10.1016/j.bmcl.2007.09.008
44443661 94119 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 503 9 1 6 6.1 CCc1nc(N(C)c2ncc(Cl)cc2Cl)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1016/j.bmcl.2007.09.008
CHEMBL249212 94119 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 503 9 1 6 6.1 CCc1nc(N(C)c2ncc(Cl)cc2Cl)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1016/j.bmcl.2007.09.008
44443636 94414 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 390 6 1 6 4.7 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(C)c(Oc2cc(C)ccn2)nc1C 10.1016/j.bmcl.2007.09.008
CHEMBL251006 94414 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 390 6 1 6 4.7 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(C)c(Oc2cc(C)ccn2)nc1C 10.1016/j.bmcl.2007.09.008
9890659 99062 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 464 3 0 7 5.2 Cc1nc(N2CCOCC2)c2sc(=S)n(-c3ccc(C(C)C)cc3Br)c2n1 10.1016/s0960-894x(99)00159-6
CHEMBL280449 99062 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 464 3 0 7 5.2 Cc1nc(N2CCOCC2)c2sc(=S)n(-c3ccc(C(C)C)cc3Br)c2n1 10.1016/s0960-894x(99)00159-6
10552595 59001 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 476 9 0 8 3.9 CCN(c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br)C(COC)COC 10.1021/jm980224g
CHEMBL169070 59001 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 476 9 0 8 3.9 CCN(c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br)C(COC)COC 10.1021/jm980224g
44384893 59907 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 382 6 0 7 3.4 CCCCN(CC)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)nc1C 10.1016/s0960-894x(99)00108-0
CHEMBL173074 59907 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 382 6 0 7 3.4 CCCCN(CC)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)nc1C 10.1016/s0960-894x(99)00108-0
11684703 71737 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 400 4 0 4 5.7 CC[C@@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL196604 71737 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 400 4 0 4 5.7 CC[C@@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
20780017 64944 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 458 7 0 4 5.2 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1Br 10.1016/j.bmcl.2005.05.117
CHEMBL182278 64944 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 458 7 0 4 5.2 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1Br 10.1016/j.bmcl.2005.05.117
44443634 93985 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 7 0 6 4.8 CCc1nc(N(C)[C@@H]2c3ccccc3C[C@@H]2OC)c(CC)nc1Oc1cc(C)ccn1 10.1016/j.bmcl.2007.09.008
CHEMBL248577 93985 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 7 0 6 4.8 CCc1nc(N(C)[C@@H]2c3ccccc3C[C@@H]2OC)c(CC)nc1Oc1cc(C)ccn1 10.1016/j.bmcl.2007.09.008
10641825 120466 0 None - 1 Rat 5.9 pKi = 5.9 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 353 2 0 3 5.1 Cc1ccc2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL354092 120466 0 None - 1 Rat 5.9 pKi = 5.9 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 353 2 0 3 5.1 Cc1ccc2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
53310410 63986 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 411 10 0 5 4.7 CCc1nc(N(CCOC)CCOC)c(CC)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
CHEMBL1807026 63986 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 411 10 0 5 4.7 CCc1nc(N(CCOC)CCOC)c(CC)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
20780074 67671 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 522 7 0 4 7.4 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC(F)(F)F)CC4CC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL190745 67671 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 522 7 0 4 7.4 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC(F)(F)F)CC4CC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
10643831 57614 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 385 10 0 6 4.5 CCCCN(CCOC)c1nc(C)nc(N(CC)c2c(C)cc(C)cc2C)n1 10.1021/jm980222w
CHEMBL166835 57614 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 385 10 0 6 4.5 CCCCN(CCOC)c1nc(C)nc(N(CC)c2c(C)cc(C)cc2C)n1 10.1021/jm980222w
9866114 65250 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 407 10 0 4 5.6 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(CC)cc(CC)cc2CC)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL182752 65250 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 407 10 0 4 5.6 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(CC)cc(CC)cc2CC)c1C 10.1016/j.bmcl.2004.05.072
44392693 66339 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 408 9 0 6 5.2 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(CC)CC)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL185055 66339 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 408 9 0 6 5.2 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N(CC)CC)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
44392753 66655 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 366 7 1 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3NC)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL185292 66655 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 366 7 1 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3NC)c(C)nn12 10.1016/j.bmcl.2004.05.056
44342015 110217 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 467 8 0 5 6.5 CCCCN(CCc1ccccn1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL323756 110217 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 467 8 0 5 6.5 CCCCN(CCc1ccccn1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9846806 110611 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 454 6 1 5 6.4 CCCN(Cc1ccc(O)cc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL325638 110611 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 454 6 1 5 6.4 CCCN(Cc1ccc(O)cc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
46891116 6811 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 454 8 0 5 5.7 CCCN(Cc1c(C(F)(F)F)nc2n(-c3ccc(OC)cc3C)c(Cl)cn12)CC1CC1 10.1016/j.bmcl.2010.04.094
CHEMBL1083922 6811 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 454 8 0 5 5.7 CCCN(Cc1c(C(F)(F)F)nc2n(-c3ccc(OC)cc3C)c(Cl)cn12)CC1CC1 10.1016/j.bmcl.2010.04.094
20780266 6886 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 6 0 4 6.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CC4CCC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1084235 6886 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 6 0 4 6.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CC4CCC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
21916134 7127 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 436 7 0 4 5.9 C=CCN(CC=C)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1085265 7127 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 436 7 0 4 5.9 C=CCN(CC=C)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
21916107 7430 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 452 7 0 4 6.3 CCN(CCC1CC1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1086594 7430 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 452 7 0 4 6.3 CCN(CCC1CC1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
11280879 67547 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 394 7 1 6 5.0 Cc1cc(NC(C)CCC(C)C)n2nc(C)c(-c3cnc(N(C)C)cc3C)c2n1 10.1021/jm040058e
CHEMBL189754 67547 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 394 7 1 6 5.0 Cc1cc(NC(C)CCC(C)C)n2nc(C)c(-c3cnc(N(C)C)cc3C)c2n1 10.1021/jm040058e
11306515 70452 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 459 7 0 5 5.7 CCCC(CCC)N1CCc2cn(-c3ccc(S(C)(=O)=O)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL194607 70452 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 459 7 0 5 5.7 CCCC(CCC)N1CCc2cn(-c3ccc(S(C)(=O)=O)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
11166658 133413 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 406 6 0 4 6.2 CCCC(CCC)N1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL370501 133413 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 406 6 0 4 6.2 CCCC(CCC)N1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
9844591 60813 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 412 6 0 6 6.1 CCCN(CC1CC1)c1nc(C)nc2c1sc(=S)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
CHEMBL17619 60813 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 412 6 0 6 6.1 CCCN(CC1CC1)c1nc(C)nc2c1sc(=S)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
44266463 4562 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 443 5 0 3 7.1 CCN(c1nc(C)cc(-c2ccccc2Cl)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10249 4562 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 443 5 0 3 7.1 CCN(c1nc(C)cc(-c2ccccc2Cl)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
44290640 101489 0 None - 1 Human 7.9 pKi = 7.9 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)c(OC)c3)c(C)nn12 10.1021/jm990590f
CHEMBL297886 101489 0 None - 1 Human 7.9 pKi = 7.9 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)c(OC)c3)c(C)nn12 10.1021/jm990590f
44266481 5372 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 427 6 0 5 5.4 CCN(c1nc(C)cc(-c2ccccc2)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
CHEMBL10698 5372 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 427 6 0 5 5.4 CCN(c1nc(C)cc(-c2ccccc2)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
122193806 123976 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 490 8 0 4 6.0 CCN(C)c1cc(C)nc2c1N(CCCCF)C(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628854 123976 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 490 8 0 4 6.0 CCN(C)c1cc(C)nc2c1N(CCCCF)C(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL2372939 210320 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)C(CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm034180+
9800789 123141 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 394 7 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3cccc(OC)c3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL361242 123141 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 394 7 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3cccc(OC)c3)c3nc(C)cc1c32 10.1021/jm050384+
44384828 59761 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 491 9 0 8 3.4 COCCN(CCOC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL172544 59761 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 491 9 0 8 3.4 COCCN(CCOC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
21916340 7380 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 502 8 0 4 7.5 CCCCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1086380 7380 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 502 8 0 4 7.5 CCCCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
10616216 103550 1 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 327 7 1 5 4.5 CCCN(CCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
CHEMBL308544 103550 1 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 327 7 1 5 4.5 CCCN(CCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
10616216 103550 1 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 327 7 1 5 4.5 CCCN(CCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
CHEMBL308544 103550 1 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 327 7 1 5 4.5 CCCN(CCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
10186078 64584 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 513 8 1 5 8.3 CCCN(Cc1cccs1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181625 64584 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 513 8 1 5 8.3 CCCN(Cc1cccs1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
18672249 64595 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 575 9 1 4 8.9 FC(F)(F)CCN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181673 64595 0 None - 1 Human 6.9 pKi = 6.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 575 9 1 4 8.9 FC(F)(F)CCN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
20780053 168949 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 497 6 0 5 6.8 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCCC4CCc4ccccc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL438847 168949 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 497 6 0 5 6.8 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCCC4CCc4ccccc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
10229290 130420 0 None - 1 Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 508 8 1 5 7.7 CCCN(Cc1ccccn1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL368018 130420 0 None - 1 Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 508 8 1 5 7.7 CCCN(Cc1ccccn1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
44389082 62549 0 None - 1 Human 4.9 pKi = 4.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 500 9 1 5 6.6 CN(C)CCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
CHEMBL178246 62549 0 None - 1 Human 4.9 pKi = 4.9 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 500 9 1 5 6.6 CN(C)CCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
11340431 73392 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 472 7 1 5 6.5 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2cccc(OCc3ccccc3)c2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL201518 73392 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 472 7 1 5 6.5 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2cccc(OCc3ccccc3)c2)c(C)c1 10.1016/j.bmcl.2005.10.097
11798911 120353 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 479 9 0 7 6.1 CCCCN(CC)c1nc(C)nc2c1nc(-c1ccccc1)n2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL353098 120353 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 479 9 0 7 6.1 CCCCN(CC)c1nc(C)nc2c1nc(-c1ccccc1)n2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
44318119 205900 0 None - 1 Human 6.9 pKi = 6.9 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 341 6 0 4 4.3 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2C)n(C)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL83934 205900 0 None - 1 Human 6.9 pKi = 6.9 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 341 6 0 4 4.3 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2C)n(C)c1=O 10.1016/s0960-894x(03)00483-9
20780073 67285 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 452 7 0 4 6.4 C=CCN(CC=C)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL188194 67285 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 452 7 0 4 6.4 C=CCN(CC=C)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
10830877 205514 0 None - 1 Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 338 7 1 4 5.1 CCCN(CC1CC1)c1cc(Nc2c(C)cc(C)cc2C)nc(C)n1 10.1021/jm960149e
CHEMBL80806 205514 0 None - 1 Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 338 7 1 4 5.1 CCCN(CC1CC1)c1cc(Nc2c(C)cc(C)cc2C)nc(C)n1 10.1021/jm960149e
10830877 205514 0 None - 1 Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 338 7 1 4 5.1 CCCN(CC1CC1)c1cc(Nc2c(C)cc(C)cc2C)nc(C)n1 10.1021/jm9900117
CHEMBL80806 205514 0 None - 1 Human 5.9 pKi = 5.9 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 338 7 1 4 5.1 CCCN(CC1CC1)c1cc(Nc2c(C)cc(C)cc2C)nc(C)n1 10.1021/jm9900117
10506052 57446 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 516 8 0 4 5.9 CCCCN(CC)c1cc(C)nc(N(CC)c2ccc(I)cc2Br)n1 10.1021/jm980222w
CHEMBL165531 57446 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 516 8 0 4 5.9 CCCCN(CC)c1cc(C)nc(N(CC)c2ccc(I)cc2Br)n1 10.1021/jm980222w
10529311 57528 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 496 10 0 5 6.5 CCN(c1nc(C)cc(N(CCOC)Cc2ccccc2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
CHEMBL166235 57528 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 496 10 0 5 6.5 CCN(c1nc(C)cc(N(CCOC)Cc2ccccc2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
44392657 65212 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3[N+](=O)[O-])c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL182567 65212 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3[N+](=O)[O-])c(C)nn12 10.1016/j.bmcl.2004.05.056
10346761 110603 1 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL 524 7 1 4 6.7 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(I)cc2Cl)c1Cl 10.1016/s0960-894x(00)00661-2
CHEMBL325577 110603 1 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL 524 7 1 4 6.7 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(I)cc2Cl)c1Cl 10.1016/s0960-894x(00)00661-2
21916292 7502 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 524 7 0 4 6.8 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN(CC2CC2)CC(F)(F)C(F)(F)F)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1087166 7502 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 524 7 0 4 6.8 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN(CC2CC2)CC(F)(F)C(F)(F)F)c(C)c1 10.1016/j.bmcl.2010.01.127
11442212 62497 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 446 8 0 5 6.2 CCCN(c1nc(-c2ccc(OC)cc2C)n(C)n1)C(CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
CHEMBL178117 62497 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 446 8 0 5 6.2 CCCN(c1nc(-c2ccc(OC)cc2C)n(C)n1)C(CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
11212115 122327 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 412 9 0 5 5.9 CCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL359863 122327 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 412 9 0 5 5.9 CCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
44337106 6253 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 356 8 1 5 3.9 CCCN(CCC)c1nc(-c2ccc(Cl)cc2Cl)n(CCO)n1 10.1016/s0960-894x(01)00657-6
CHEMBL108158 6253 0 None - 1 Human 7.9 pKi = 7.9 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 356 8 1 5 3.9 CCCN(CCC)c1nc(-c2ccc(Cl)cc2Cl)n(CCO)n1 10.1016/s0960-894x(01)00657-6
122193726 123966 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 474 6 0 4 5.4 Cc1cc(N(C)C)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2C/C=C/CF 10.1016/j.bmcl.2015.10.010
CHEMBL3628745 123966 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 474 6 0 4 5.4 Cc1cc(N(C)C)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2C/C=C/CF 10.1016/j.bmcl.2015.10.010
9946605 64003 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 353 6 1 4 5.4 CCC(CC)Nc1nc(OC)c(-c2ccc(Cl)cc2Cl)nc1C 10.1021/jm200365y
CHEMBL1807043 64003 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 353 6 1 4 5.4 CCC(CC)Nc1nc(OC)c(-c2ccc(Cl)cc2Cl)nc1C 10.1021/jm200365y
9957428 61279 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 494 9 0 8 4.1 COCCN(CCOC)c1nc(C)nc2c1sc(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
CHEMBL17666 61279 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 494 9 0 8 4.1 COCCN(CCOC)c1nc(C)nc2c1sc(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
9798798 63152 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 356 4 0 6 3.9 CCN(CC)c1nc(C)nc2c1sc(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
CHEMBL17897 63152 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 356 4 0 6 3.9 CCN(CC)c1nc(C)nc2c1sc(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
44341687 111316 1 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 378 8 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL326722 111316 1 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 378 8 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)cccc12 10.1016/s0960-894x(03)00684-x
11475328 126187 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 408 8 0 6 4.7 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(OCC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL364938 126187 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 408 8 0 6 4.7 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(OCC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
44341634 10258 1 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 317 2 0 2 5.5 COc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL116106 10258 1 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 317 2 0 2 5.5 COc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
20780054 169130 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 409 3 0 6 4.1 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCOCC4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL440232 169130 0 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 409 3 0 6 4.1 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCOCC4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
11109264 102559 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 297 5 2 4 3.4 COc1cccc(N/C(=N/Nc2ccccc2C)C(C)=O)c1 10.1021/jm025512y
CHEMBL304072 102559 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 297 5 2 4 3.4 COc1cccc(N/C(=N/Nc2ccccc2C)C(C)=O)c1 10.1021/jm025512y
20780180 67204 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 468 7 0 4 6.8 CCN(CCC1CC1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL187815 67204 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 468 7 0 4 6.8 CCN(CCC1CC1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
11782614 203959 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 335 4 2 3 4.3 CC(=O)/C(=N\c1cccc(C)c1)NNc1ccccc1C(F)(F)F 10.1021/jm025512y
CHEMBL69374 203959 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 335 4 2 3 4.3 CC(=O)/C(=N\c1cccc(C)c1)NNc1ccccc1C(F)(F)F 10.1021/jm025512y
44308156 102331 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 420 7 0 6 4.4 CCCN(CCN(C)C)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL303639 102331 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 420 7 0 6 4.4 CCCN(CCN(C)C)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
11245983 75913 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 380 4 1 4 5.2 Cc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
CHEMBL204967 75913 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 380 4 1 4 5.2 Cc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
1799083 204013 3 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 365 4 2 3 4.3 CC(=O)/C(=N\c1cccc(Cl)c1)NNc1ccc(Br)cc1 10.1021/jm025512y
CHEMBL69686 204013 3 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 365 4 2 3 4.3 CC(=O)/C(=N\c1cccc(Cl)c1)NNc1ccc(Br)cc1 10.1021/jm025512y
10594766 103136 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 361 6 1 5 4.9 CCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
CHEMBL307871 103136 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 361 6 1 5 4.9 CCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
10594766 103136 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 361 6 1 5 4.9 CCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
CHEMBL307871 103136 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 361 6 1 5 4.9 CCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
22324320 205948 0 None - 1 Human 7.8 pKi = 7.8 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 381 7 0 4 5.2 CCCN(CCC)c1c(C)nc(-c2ccc(Cl)cc2Cl)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL84339 205948 0 None - 1 Human 7.8 pKi = 7.8 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 381 7 0 4 5.2 CCCN(CCC)c1c(C)nc(-c2ccc(Cl)cc2Cl)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
10596113 120586 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 382 7 0 5 5.1 CCN(CC)c1cc(C)nc(N(CC)c2c(Cl)cc(OC)cc2Cl)n1 10.1021/jm980222w
CHEMBL354584 120586 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 382 7 0 5 5.1 CCN(CC)c1cc(C)nc(N(CC)c2c(Cl)cc(OC)cc2Cl)n1 10.1021/jm980222w
10474043 64577 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 365 7 0 4 4.9 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL181593 64577 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 365 7 0 4 4.9 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
4183319 114749 1 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 352 7 0 5 4.6 CCCN(CCC)c1cc(C)nc2c(-c3ccccc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL333880 114749 1 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 352 7 0 5 4.6 CCCN(CCC)c1cc(C)nc2c(-c3ccccc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
44306488 202749 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 395 9 0 5 5.2 CCCN(c1ncc(C)c(-c2c(C)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL61954 202749 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 395 9 0 5 5.2 CCCN(c1ncc(C)c(-c2c(C)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
9865575 203397 1 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 397 10 0 6 4.6 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL65484 203397 1 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 397 10 0 6 4.6 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
44308017 102531 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 379 7 0 5 5.4 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)nn(CC)c12 10.1016/s0960-894x(02)00358-x
CHEMBL304059 102531 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 379 7 0 5 5.4 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)nn(CC)c12 10.1016/s0960-894x(02)00358-x
44305208 100747 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 356 6 0 4 5.3 CCCCN(CC)c1cc(C)nc2c(-c3ccccc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL292764 100747 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 356 6 0 4 5.3 CCCCN(CC)c1cc(C)nc2c(-c3ccccc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
20780153 93761 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 449 8 0 5 6.3 CCCN(CCC1CC1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL247359 93761 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 449 8 0 5 6.3 CCCN(CCC1CC1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
20780142 145063 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 415 7 0 5 5.5 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
CHEMBL391141 145063 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 415 7 0 5 5.5 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
20780165 147760 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 423 7 0 5 5.9 CCCN(CCC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL393250 147760 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 423 7 0 5 5.9 CCCN(CCC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
10132995 187991 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 357 8 0 5 4.7 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL497301 187991 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 357 8 0 5 4.7 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
11375016 124078 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 478 7 0 6 6.4 CCCN(Cc1ccc2ccccc2c1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL363269 124078 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 478 7 0 6 6.4 CCCN(Cc1ccc2ccccc2c1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
44337304 109883 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 396 7 0 4 5.3 CCCN(c1nc(-c2cc(F)c(Cl)cc2Cl)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL323437 109883 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 396 7 0 4 5.3 CCCN(c1nc(-c2cc(F)c(Cl)cc2Cl)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
44387103 61786 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 473 8 1 6 5.7 CCCCC(CC)Nc1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL177310 61786 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 473 8 1 6 5.7 CCCCC(CC)Nc1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
10717531 58510 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 430 10 0 9 3.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1SC 10.1021/jm980224g
CHEMBL168388 58510 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 430 10 0 9 3.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1SC 10.1021/jm980224g
10812125 59135 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 421 7 0 7 4.2 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(N(C)C)cc1C(F)(F)F 10.1021/jm980224g
CHEMBL169862 59135 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 421 7 0 7 4.2 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(N(C)C)cc1C(F)(F)F 10.1021/jm980224g
11656502 71197 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 402 4 0 4 6.0 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC(C)C 10.1021/jm049085v
CHEMBL195636 71197 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 402 4 0 4 6.0 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC(C)C 10.1021/jm049085v
11361057 67672 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 382 6 0 7 3.1 CCCC(OC)N1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL190757 67672 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 382 6 0 7 3.1 CCCC(OC)N1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
21916165 67231 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 446 8 0 4 6.5 CCCN(Cc1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ccc(F)cc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL187940 67231 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 446 8 0 4 6.5 CCCN(Cc1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ccc(F)cc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
44397642 67558 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 546 8 0 4 7.8 CCCN(Cc1c(C(F)(F)F)nc2n(-c3ccc(C(C)C)cc3Br)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL189809 67558 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 546 8 0 4 7.8 CCCN(Cc1c(C(F)(F)F)nc2n(-c3ccc(C(C)C)cc3Br)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
44347117 16447 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 466 7 0 6 5.0 CCCN(CC1CC1)c1cc(S(C)(=O)=O)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL123306 16447 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 466 7 0 6 5.0 CCCN(CC1CC1)c1cc(S(C)(=O)=O)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.019
21916109 6706 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 533 8 0 6 7.0 CCCN(Cc1ccc([N+](=O)[O-])cc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1083612 6706 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 533 8 0 6 7.0 CCCN(Cc1ccc([N+](=O)[O-])cc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
21916289 6876 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 474 6 0 4 6.4 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)CCc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1084184 6876 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 474 6 0 4 6.4 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)CCc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
10502620 119419 0 None - 1 Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 426 7 0 4 6.4 CCCN(CC1CC1)c1nc(C)nc(N(C)c2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm960149e
CHEMBL344805 119419 0 None - 1 Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 426 7 0 4 6.4 CCCN(CC1CC1)c1nc(C)nc(N(C)c2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm960149e
10275456 63377 0 None - 1 Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 445 7 1 4 7.1 CCCN(CC)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL179576 63377 0 None - 1 Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 445 7 1 4 7.1 CCCN(CC)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
11429073 62618 0 None - 1 Human 6.8 pKi = 6.8 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 384 7 0 5 5.1 CCC(c1ccccc1)N(CC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL178346 62618 0 None - 1 Human 6.8 pKi = 6.8 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 384 7 0 5 5.1 CCC(c1ccccc1)N(CC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
44337446 5200 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 420 8 0 4 5.8 CCCN(c1nc(-c2c(C)cc(C)cc2C)n(CC(F)(F)F)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL106093 5200 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 420 8 0 4 5.8 CCCN(c1nc(-c2c(C)cc(C)cc2C)n(CC(F)(F)F)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
22248956 63996 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 381 8 1 4 6.0 CCOc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1807036 63996 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 381 8 1 4 6.0 CCOc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(CC)CC 10.1021/jm200365y
46881398 7505 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 408 3 0 5 4.2 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN2CCOCC2)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1087173 7505 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 408 3 0 5 4.2 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN2CCOCC2)c(C)c1 10.1016/j.bmcl.2010.01.127
22249081 63987 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 408 9 0 4 5.4 CCCN(CCN(C)C)c1nc(CC)c(-c2ccc(Cl)cc2Cl)nc1CC 10.1021/jm200365y
CHEMBL1807027 63987 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 408 9 0 4 5.4 CCCN(CCN(C)C)c1nc(CC)c(-c2ccc(Cl)cc2Cl)nc1CC 10.1021/jm200365y
44460260 205338 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 398 7 1 3 6.1 Cc1ccccc1[C@@H](Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
CHEMBL79587 205338 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 398 7 1 3 6.1 Cc1ccccc1[C@@H](Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
44443575 93986 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 414 8 2 4 6.9 CCc1nc(NC(CC)CC)c(CC)nc1Nc1c(Cl)cc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.008
CHEMBL248585 93986 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 414 8 2 4 6.9 CCc1nc(NC(CC)CC)c(CC)nc1Nc1c(Cl)cc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.008
20780024 65225 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 472 8 0 4 5.7 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2005.05.117
CHEMBL182624 65225 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 472 8 0 4 5.7 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2005.05.117
11454794 75609 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 497 7 1 6 6.3 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCc3ccc(C#N)cc3)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL204706 75609 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 497 7 1 6 6.3 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCc3ccc(C#N)cc3)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
11704536 71765 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 424 5 0 6 4.9 CC[C@H]1Cn2nc(-c3ccc(C(=O)OC)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL196682 71765 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 424 5 0 6 4.9 CC[C@H]1Cn2nc(-c3ccc(C(=O)OC)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
9843989 71919 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 400 2 0 4 5.9 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3CCN2C1CCCCC1 10.1021/jm049085v
CHEMBL197204 71919 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 400 2 0 4 5.9 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3CCN2C1CCCCC1 10.1021/jm049085v
11524923 124806 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 436 4 0 4 6.5 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1Cc1ccccc1 10.1021/jm049085v
CHEMBL364261 124806 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 436 4 0 4 6.5 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1Cc1ccccc1 10.1021/jm049085v
44352386 18962 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 451 8 1 4 7.1 CCCN(Cc1sc(Nc2c(C)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL128709 18962 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 451 8 1 4 7.1 CCCN(Cc1sc(Nc2c(C)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
44341635 10001 1 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 333 2 0 2 6.2 CSc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL114914 10001 1 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 333 2 0 2 6.2 CSc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
46891210 6638 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 7 0 4 6.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)CC4CC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1083320 6638 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 7 0 4 6.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)CC4CC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
20780253 6949 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 452 6 0 4 6.3 CCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC1CCC1 10.1016/j.bmcl.2010.04.094
CHEMBL1084511 6949 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 452 6 0 4 6.3 CCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC1CCC1 10.1016/j.bmcl.2010.04.094
44307870 203543 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 377 5 1 5 5.2 CCC(CC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL66492 203543 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 377 5 1 5 5.2 CCC(CC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
44307654 203567 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 351 6 1 4 4.8 CCCN(CCC)c1[nH]c(C)nc2c(-c3c(C)cc(C)cc3C)nnc1-2 10.1016/s0960-894x(02)00358-x
CHEMBL66719 203567 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 351 6 1 4 4.8 CCCN(CCC)c1[nH]c(C)nc2c(-c3c(C)cc(C)cc3C)nnc1-2 10.1016/s0960-894x(02)00358-x
21916343 93380 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 469 7 0 5 6.2 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
CHEMBL245671 93380 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 469 7 0 5 6.2 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
44587491 188119 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 371 9 0 5 5.1 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OCC 10.1016/j.bmcl.2008.07.063
CHEMBL498318 188119 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 371 9 0 5 5.1 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OCC 10.1016/j.bmcl.2008.07.063
11235868 135184 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 397 5 0 4 5.4 CCC(COC)N1CCc2cn(-c3c(C)cc(Cl)cc3C)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL372009 135184 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 397 5 0 4 5.4 CCC(COC)N1CCc2cn(-c3c(C)cc(Cl)cc3C)c3nc(C)cc1c23 10.1021/jm050070m
44341452 9515 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 446 9 0 4 7.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C(C)C)c12 10.1016/s0960-894x(03)00621-8
CHEMBL112151 9515 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 446 9 0 4 7.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C(C)C)c12 10.1016/s0960-894x(03)00621-8
9843717 66778 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 396 6 0 6 4.7 CCCN(CC1CC1)c1nc(C)nc2c1sc(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
CHEMBL18590 66778 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 396 6 0 6 4.7 CCCN(CC1CC1)c1nc(C)nc2c1sc(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
11166649 106425 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 442 10 0 6 5.9 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2cc(OC)c(OC)cc2Cl)n(C)n1 10.1021/jm049339c
CHEMBL3085418 106425 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 442 10 0 6 5.9 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2cc(OC)c(OC)cc2Cl)n(C)n1 10.1021/jm049339c
CHEMBL3139572 106425 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 442 10 0 6 5.9 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2cc(OC)c(OC)cc2Cl)n(C)n1 10.1021/jm049339c
122193722 123963 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 416 4 1 4 4.8 CCN(C)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628742 123963 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 416 4 1 4 4.8 CCN(C)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
135444727 120224 0 None -3 2 Rat 6.8 pKi = 6.8 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 428 3 4 7 2.4 NCCNC(=O)c1c2c(c3c(O)c4ccccc4c4ncnc1c34)=N[C@@H]1CCCC[C@H]1N2 10.1016/s0960-894x(99)00075-x
CHEMBL352154 120224 0 None -3 2 Rat 6.8 pKi = 6.8 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 428 3 4 7 2.4 NCCNC(=O)c1c2c(c3c(O)c4ccccc4c4ncnc1c34)=N[C@@H]1CCCC[C@H]1N2 10.1016/s0960-894x(99)00075-x
21916299 6406 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 460 5 0 4 6.4 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082339 6406 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 460 5 0 4 6.4 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
21916288 6699 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 546 6 0 4 7.4 Cc1cc(C)c(-n2c(Cl)cn3c(CN(Cc4ccc(F)cc4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1083593 6699 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 546 6 0 4 7.4 Cc1cc(C)c(-n2c(Cl)cn3c(CN(Cc4ccc(F)cc4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
10276375 63276 0 None - 1 Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 459 8 1 4 7.5 CCCN(CCC)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL179225 63276 0 None - 1 Human 6.8 pKi = 6.8 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 459 8 1 4 7.5 CCCN(CCC)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
20780156 123675 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 544 8 0 4 8.1 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3ccc(Cl)cc3Cl)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL362124 123675 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 544 8 0 4 8.1 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3ccc(Cl)cc3Cl)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
46891009 6435 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 3 0 4 6.1 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCCCC4C)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082442 6435 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 3 0 4 6.1 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCCCC4C)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
10273816 19378 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 421 7 1 5 5.3 CCN(CCOC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
CHEMBL129196 19378 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 421 7 1 5 5.3 CCN(CCOC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
44587372 187989 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 387 10 1 6 4.1 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OCCO 10.1016/j.bmcl.2008.07.063
CHEMBL497286 187989 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 387 10 1 6 4.1 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OCCO 10.1016/j.bmcl.2008.07.063
44462061 106591 0 None - 1 Human 5.8 pKi = 5.8 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 425 8 0 5 5.0 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(CC(F)(F)F)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL314267 106591 0 None - 1 Human 5.8 pKi = 5.8 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 425 8 0 5 5.0 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(CC(F)(F)F)c1=O 10.1016/s0960-894x(03)00483-9
44446732 94869 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 334 5 1 3 5.7 CCCNc1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253915 94869 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 334 5 1 3 5.7 CCCNc1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
22249005 63992 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 355 6 1 3 5.8 CCc1nc(NC(CC)CC)c(F)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
CHEMBL1807032 63992 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 355 6 1 3 5.8 CCc1nc(NC(CC)CC)c(F)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
44446717 155431 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 352 6 0 2 6.5 CCCN(CCC)c1c(C)nc(-c2ccccc2Cl)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL403745 155431 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 352 6 0 2 6.5 CCCN(CCC)c1c(C)nc(-c2ccccc2Cl)c2ccccc12 10.1016/j.bmcl.2007.12.050
10787219 205171 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 401 5 2 5 5.5 Cc1cc(C)c(Nc2nc(C)nc(NCc3ccc(C(F)(F)F)cc3)n2)c(C)c1 10.1021/jm960148m
CHEMBL78271 205171 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 401 5 2 5 5.5 Cc1cc(C)c(Nc2nc(C)nc(NCc3ccc(C(F)(F)F)cc3)n2)c(C)c1 10.1021/jm960148m
10787219 205171 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 401 5 2 5 5.5 Cc1cc(C)c(Nc2nc(C)nc(NCc3ccc(C(F)(F)F)cc3)n2)c(C)c1 10.1021/jm9900117
CHEMBL78271 205171 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 401 5 2 5 5.5 Cc1cc(C)c(Nc2nc(C)nc(NCc3ccc(C(F)(F)F)cc3)n2)c(C)c1 10.1021/jm9900117
9954503 67552 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 432 6 0 5 5.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(C(F)(F)F)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL189780 67552 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 432 6 0 5 5.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(C(F)(F)F)cc3)c3nc(C)cc1c32 10.1021/jm050384+
10669045 58140 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 405 7 0 6 4.1 CCN(CC)c1nc(C)nc(N(CC)c2ccc(C(C)=O)cc2Br)n1 10.1021/jm980222w
CHEMBL167853 58140 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 405 7 0 6 4.1 CCN(CC)c1nc(C)nc(N(CC)c2ccc(C(C)=O)cc2Br)n1 10.1021/jm980222w
10647940 120723 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 466 8 0 4 6.9 CCN(Cc1ccccc1)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL354791 120723 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 466 8 0 4 6.9 CCN(Cc1ccccc1)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
44392709 129896 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 420 7 0 6 5.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N4CCCCC4)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL367583 129896 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 420 7 0 6 5.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N4CCCCC4)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
44308187 204052 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 375 3 1 5 5.0 Cc1nc(NC2CCCC2)c2nn(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(02)00358-x
CHEMBL69968 204052 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 375 3 1 5 5.0 Cc1nc(NC2CCCC2)c2nn(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(02)00358-x
20780144 150989 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 443 8 0 5 6.2 CCCN(Cc1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CCC1 10.1016/j.bmcl.2007.01.008
CHEMBL395833 150989 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 443 8 0 5 6.2 CCCN(Cc1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CCC1 10.1016/j.bmcl.2007.01.008
11454873 140755 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 502 8 1 6 6.5 COc1ccccc1COc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
CHEMBL381824 140755 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 502 8 1 6 6.5 COc1ccccc1COc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
44446724 94807 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 414 9 0 4 6.4 CCCN(CCC)c1c(C)nc(-c2ccc(OC(F)F)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253493 94807 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 414 9 0 4 6.4 CCCN(CCC)c1c(C)nc(-c2ccc(OC(F)F)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
11485413 166155 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 5 1 6 4.2 Cc1cc(NC(C)C(C)C)n2nc(C)c(-c3cnc(N(C)C)cc3C)c2n1 10.1021/jm040058e
CHEMBL426260 166155 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 5 1 6 4.2 Cc1cc(NC(C)C(C)C)n2nc(C)c(-c3cnc(N(C)C)cc3C)c2n1 10.1021/jm040058e
22249061 63980 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 359 9 1 7 3.7 CCc1nc(-c2cnc(OC)nc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1807020 63980 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 359 9 1 7 3.7 CCc1nc(-c2cnc(OC)nc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
44384750 131801 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 395 7 1 6 4.7 CCCCC(CC)Nc1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00108-0
CHEMBL369371 131801 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 395 7 1 6 4.7 CCCCC(CC)Nc1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00108-0
44266437 208408 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 5 0 3 7.5 CCN(c1nc(C)cc(-c2cccc(C(F)(F)F)c2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL9975 208408 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 5 0 3 7.5 CCN(c1nc(C)cc(-c2cccc(C(F)(F)F)c2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
11429605 124537 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 404 4 0 5 4.5 CCC(CC)N1CCn2c(=O)n(-c3ccc(C(F)(F)F)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL364037 124537 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 404 4 0 5 4.5 CCC(CC)N1CCn2c(=O)n(-c3ccc(C(F)(F)F)cc3)c3nc(C)cc1c32 10.1021/jm050384+
44341983 9539 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 362 5 1 4 5.5 CCCCNc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112266 9539 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 362 5 1 4 5.5 CCCCNc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
21916286 6703 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 488 7 0 4 7.1 CCCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1083608 6703 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 488 7 0 4 7.1 CCCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
46891057 7283 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 426 3 0 5 4.6 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCOCC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1086016 7283 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 426 3 0 5 4.6 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCOCC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
20780039 6690 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 444 7 0 4 5.8 CCCN(CCc1ccccc1)C(=O)c1c(C)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
CHEMBL1083513 6690 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 444 7 0 4 5.8 CCCN(CCc1ccccc1)C(=O)c1c(C)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
10785716 28291 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 375 8 1 5 5.1 CCc1cccc(CC)c1Nc1nc(C)nc(N(CC)Cc2ccccc2)n1 10.1021/jm960148m
CHEMBL137434 28291 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 375 8 1 5 5.1 CCc1cccc(CC)c1Nc1nc(C)nc(N(CC)Cc2ccccc2)n1 10.1021/jm960148m
44446737 155608 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 459 10 0 4 6.9 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCCC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL404559 155608 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 459 10 0 4 6.9 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCCC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
44443658 154919 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 489 9 2 6 6.1 CCc1nc(N[C@@H]2c3ccccc3C[C@@H]2OCCF)c(CC)nc1Nc1ncc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.008
CHEMBL400952 154919 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 489 9 2 6 6.1 CCc1nc(N[C@@H]2c3ccccc3C[C@@H]2OCCF)c(CC)nc1Nc1ncc(Cl)cc1Cl 10.1016/j.bmcl.2007.09.008
44307479 203555 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 389 3 1 5 5.4 Cc1nc(NC2CCCCC2)c2nn(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(02)00358-x
CHEMBL66631 203555 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 389 3 1 5 5.4 Cc1nc(NC2CCCCC2)c2nn(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(02)00358-x
44407869 75117 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 394 4 1 4 5.5 Cc1ccc(S(=O)(=O)c2c(C)cc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
CHEMBL203609 75117 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 394 4 1 4 5.5 Cc1ccc(S(=O)(=O)c2c(C)cc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
44379386 120753 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 465 11 0 7 4.3 CCN(c1nc(C)nc(N(CCOC)CCOC)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
CHEMBL355055 120753 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 465 11 0 7 4.3 CCN(c1nc(C)nc(N(CCOC)CCOC)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
44341823 10006 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 434 9 0 5 5.9 CCCCN(CCCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL114928 10006 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 434 9 0 5 5.9 CCCCN(CCCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
20780123 195612 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 451 9 0 5 6.7 CCCCN(CCCC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL556060 195612 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 451 9 0 5 6.7 CCCCN(CCCC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
44379486 120032 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 432 9 0 4 6.5 CCCCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm049737f
CHEMBL350356 120032 0 None - 1 Human 7.8 pKi = 7.8 Binding
Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1Inhibition of [125I]ovine-CRF binding to corticotropin releasing factor receptor 1
ChEMBL 432 9 0 4 6.5 CCCCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm049737f
18691318 97160 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 423 5 0 3 6.8 CCN(c1nc(C)cc(-c2ccccc2C)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL268043 97160 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 423 5 0 3 6.8 CCN(c1nc(C)cc(-c2ccccc2C)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
135958362 58166 0 None -2 2 Rat 6.8 pKi = 6.8 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 482 2 4 7 3.7 N[C@@H]1CCCC[C@H]1NC(=O)c1c2c(c3c(O)c4ccccc4c4ncnc1c34)=N[C@H]1CCCC[C@@H]1N2 10.1016/s0960-894x(99)00075-x
CHEMBL168162 58166 0 None -2 2 Rat 6.8 pKi = 6.8 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 482 2 4 7 3.7 N[C@@H]1CCCC[C@H]1NC(=O)c1c2c(c3c(O)c4ccccc4c4ncnc1c34)=N[C@H]1CCCC[C@@H]1N2 10.1016/s0960-894x(99)00075-x
44392788 123751 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 387 6 0 4 5.8 CCCN(c1ccccc1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL362224 123751 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 387 6 0 4 5.8 CCCN(c1ccccc1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
44341612 110674 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 446 10 0 4 7.5 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(CCC)c12 10.1016/s0960-894x(03)00621-8
CHEMBL325960 110674 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 446 10 0 4 7.5 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(CCC)c12 10.1016/s0960-894x(03)00621-8
20779996 6590 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 450 5 0 5 5.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)Cc4ccco4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1083101 6590 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 450 5 0 5 5.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)Cc4ccco4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
122193721 123962 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 402 3 1 4 4.4 Cc1cc(N(C)C)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2 10.1016/j.bmcl.2015.10.010
CHEMBL3628741 123962 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 402 3 1 4 4.4 Cc1cc(N(C)C)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2 10.1016/j.bmcl.2015.10.010
10204577 122027 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 454 5 1 5 6.7 CCc1nccn1Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL359494 122027 0 None - 1 Human 5.8 pKi = 5.8 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 454 5 1 5 6.7 CCc1nccn1Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
44389071 63354 0 None - 1 Human 4.8 pKi = 4.8 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 426 4 1 5 6.1 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1Cn1ccnc1 10.1016/j.bmcl.2004.10.055
CHEMBL179480 63354 0 None - 1 Human 4.8 pKi = 4.8 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 426 4 1 5 6.1 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1Cn1ccnc1 10.1016/j.bmcl.2004.10.055
11141163 163605 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 301 4 2 3 3.9 CC(=O)/C(=N\c1ccc(Cl)cc1)NNc1ccccc1C 10.1021/jm025512y
CHEMBL420361 163605 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 301 4 2 3 3.9 CC(=O)/C(=N\c1ccc(Cl)cc1)NNc1ccccc1C 10.1021/jm025512y
10663467 57509 1 None - 1 Rat 6.7 pKi = 6.7 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 319 3 0 3 4.2 CCc1ccc(N(C)c2nc(C)cc(C)n2)c(Br)c1 10.1021/jm980222w
CHEMBL166102 57509 1 None - 1 Rat 6.7 pKi = 6.7 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 319 3 0 3 4.2 CCc1ccc(N(C)c2nc(C)cc(C)n2)c(Br)c1 10.1021/jm980222w
44379486 120032 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 432 9 0 4 6.5 CCCCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL350356 120032 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 432 9 0 4 6.5 CCCCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
44392644 123021 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 355 6 0 5 4.5 CCCN(CCC)c1cc(C)nc2c(-c3ncc(F)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL360905 123021 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 355 6 0 5 4.5 CCCN(CCC)c1cc(C)nc2c(-c3ncc(F)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
44306220 100869 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 381 9 0 5 4.9 CCCN(c1ncc(C)c(-c2ccc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL293627 100869 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 381 9 0 5 4.9 CCCN(c1ncc(C)c(-c2ccc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
46881397 7503 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 432 6 0 4 5.2 C=CCN(CC=C)C(=O)c1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
CHEMBL1087167 7503 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 432 6 0 4 5.2 C=CCN(CC=C)C(=O)c1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
10111096 63985 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 391 8 0 3 6.2 CCCN(CC1CC1)c1nc(CC)c(-c2ccc(Cl)cc2Cl)nc1CC 10.1021/jm200365y
CHEMBL1807025 63985 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 391 8 0 3 6.2 CCCN(CC1CC1)c1nc(CC)c(-c2ccc(Cl)cc2Cl)nc1CC 10.1021/jm200365y
10694719 59055 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 446 6 1 8 3.8 CCC(Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br)C(=O)OC 10.1021/jm980224g
CHEMBL169460 59055 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 446 6 1 8 3.8 CCC(Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br)C(=O)OC 10.1021/jm980224g
11568262 70285 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 434 4 0 4 6.1 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3C(F)(F)F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL194295 70285 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 434 4 0 4 6.1 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3C(F)(F)F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11713460 135572 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 414 4 0 4 6.1 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC1CCC1 10.1021/jm049085v
CHEMBL372905 135572 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 414 4 0 4 6.1 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC1CCC1 10.1021/jm049085v
44462060 205905 0 None - 1 Human 6.7 pKi = 6.7 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 385 9 0 5 4.9 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(CCC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL83970 205905 0 None - 1 Human 6.7 pKi = 6.7 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 385 9 0 5 4.9 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(CCC)c1=O 10.1016/s0960-894x(03)00483-9
11441545 67579 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 420 5 0 6 4.1 CCCC(OC)N1CCn2c(=O)n(-c3ccc(C(F)(F)F)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL190037 67579 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 420 5 0 6 4.1 CCCC(OC)N1CCn2c(=O)n(-c3ccc(C(F)(F)F)cc3)c3nc(C)cc1c32 10.1021/jm050384+
21916311 7300 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 500 5 0 4 6.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCCC4Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1086061 7300 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 500 5 0 4 6.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCCC4Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
11188091 168423 0 None - 1 Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 377 7 0 4 5.7 CCCC(CCC)N1CCc2cn(-c3cccc(OC)c3)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL434910 168423 0 None - 1 Human 6.7 pKi = 6.7 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 377 7 0 4 5.7 CCCC(CCC)N1CCc2cn(-c3cccc(OC)c3)c3nc(C)cc1c23 10.1021/jm050070m
44392777 65484 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 401 10 1 7 3.5 CCCN(CC1CC1)c1cc(C(O)c2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL183037 65484 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 401 10 1 7 3.5 CCCN(CC1CC1)c1cc(C(O)c2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
44392750 125518 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 415 10 1 7 3.7 CCCN(CC1CC1)c1cc(C(C)(O)c2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL364640 125518 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 415 10 1 7 3.7 CCCN(CC1CC1)c1cc(C(C)(O)c2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
46890889 6597 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 475 6 0 5 5.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)CCc4cccnc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1083119 6597 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 475 6 0 5 5.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)CCc4cccnc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
46890950 7299 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 556 8 0 4 7.7 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCc4ccccc4)CCC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1086059 7299 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 556 8 0 4 7.7 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCc4ccccc4)CCC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
11223591 68612 0 None - 1 Human 5.7 pKi = 5.7 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 409 7 0 3 6.7 CCCC(CCC)N1CCc2cn(Cc3ccc(Cl)cc3C)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL191780 68612 0 None - 1 Human 5.7 pKi = 5.7 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 409 7 0 3 6.7 CCCC(CCC)N1CCc2cn(Cc3ccc(Cl)cc3C)c3nc(C)cc1c23 10.1021/jm050070m
20780284 63503 0 None - 1 Human 4.7 pKi = 4.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 380 8 0 4 5.1 CCCN(Cc1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C)CC1CC1 10.1016/j.bmcl.2005.05.117
CHEMBL179985 63503 0 None - 1 Human 4.7 pKi = 4.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 380 8 0 4 5.1 CCCN(Cc1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C)CC1CC1 10.1016/j.bmcl.2005.05.117
44389113 64612 0 None - 1 Human 4.7 pKi = 4.7 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 474 8 1 5 6.2 CCN(CCN(C)C)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181732 64612 0 None - 1 Human 4.7 pKi = 4.7 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 474 8 1 5 6.2 CCN(CCN(C)C)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
44307893 203475 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 335 3 1 5 4.1 CCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL66052 203475 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 335 3 1 5 4.1 CCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
10501205 59086 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 400 3 0 6 4.0 Cc1nc(N2CCCC2)c2nnn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980224g
CHEMBL169629 59086 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 400 3 0 6 4.0 Cc1nc(N2CCCC2)c2nnn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980224g
10741433 120368 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 6 1 7 4.2 COCC(C)(C)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL353238 120368 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 6 1 7 4.2 COCC(C)(C)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
11078292 168210 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 339 4 2 3 4.1 CC(=O)/C(=N\c1cccc(F)c1)NNc1ccccc1C(F)(F)F 10.1021/jm025512y
CHEMBL433505 168210 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 339 4 2 3 4.1 CC(=O)/C(=N\c1cccc(F)c1)NNc1ccccc1C(F)(F)F 10.1021/jm025512y
11474959 75298 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 396 5 1 5 4.9 COc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
CHEMBL203744 75298 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 396 5 1 5 4.9 COc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
10028059 102886 0 None - 1 Human 8.7 pKi = 8.7 Binding
Ability to inhibit [125I]CRH binding to human Corticotropin releasing factor receptor 1Ability to inhibit [125I]CRH binding to human Corticotropin releasing factor receptor 1
ChEMBL 476 7 1 4 6.9 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1Br 10.1021/jm9900117
CHEMBL305900 102886 0 None - 1 Human 8.7 pKi = 8.7 Binding
Ability to inhibit [125I]CRH binding to human Corticotropin releasing factor receptor 1Ability to inhibit [125I]CRH binding to human Corticotropin releasing factor receptor 1
ChEMBL 476 7 1 4 6.9 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1Br 10.1021/jm9900117
CHEMBL2372950 210321 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CCCC)NC(=O)[C@H](CCCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(C)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)[C@H](N)Cc2ccccc2)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N1)C(=O)CN[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm034180+
9843598 67776 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 394 7 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL190845 67776 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 394 7 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
10835052 58090 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 403 7 0 3 6.7 CCC(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL167407 58090 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 403 7 0 3 6.7 CCC(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL263451 210572 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity of the receptor corticotropin releasing factor receptor with peptidic agonistsBinding affinity of the receptor corticotropin releasing factor receptor with peptidic agonists
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)[C@@H](N)Cc2ccccc2)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@H](Cc2c[nH]cn2)C(=O)N1)[C@@H](C)CC)C(N)=O 10.1021/jm990590f
10344587 167844 0 None -1 2 Human 8.7 pKi = 8.7 Binding
Binding affinity to CRF1 receptor (unknown origin)Binding affinity to CRF1 receptor (unknown origin)
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1016/j.bmcl.2013.02.009
CHEMBL1762817 167844 0 None -1 2 Human 8.7 pKi = 8.7 Binding
Binding affinity to CRF1 receptor (unknown origin)Binding affinity to CRF1 receptor (unknown origin)
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1016/j.bmcl.2013.02.009
CHEMBL430892 167844 0 None -1 2 Human 8.7 pKi = 8.7 Binding
Binding affinity to CRF1 receptor (unknown origin)Binding affinity to CRF1 receptor (unknown origin)
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1016/j.bmcl.2013.02.009
10344587 167844 0 None -1 2 Human 8.7 pKi = 8.7 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1016/j.bmcl.2012.08.112
CHEMBL1762817 167844 0 None -1 2 Human 8.7 pKi = 8.7 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1016/j.bmcl.2012.08.112
CHEMBL430892 167844 0 None -1 2 Human 8.7 pKi = 8.7 Binding
Binding affinity to CRFR1 by autoradiographyBinding affinity to CRFR1 by autoradiography
ChEMBL 467 8 0 7 3.9 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Br)cc3Cl)c(C)nn12 10.1016/j.bmcl.2012.08.112
44341832 9418 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
CHEMBL111665 9418 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
44341832 9418 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL111665 9418 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
44307738 100813 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cellsDisplacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cells
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/j.bmc.2017.10.012
CHEMBL293228 100813 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cellsDisplacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cells
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/j.bmc.2017.10.012
44307491 102292 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cellsDisplacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cells
ChEMBL 391 6 0 5 5.3 CCCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/j.bmc.2017.10.012
CHEMBL303380 102292 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cellsDisplacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cells
ChEMBL 391 6 0 5 5.3 CCCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/j.bmc.2017.10.012
176157 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2005.05.117
3512 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2005.05.117
CHEMBL45281 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2005.05.117
44307738 100813 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL293228 100813 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
44307491 102292 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 391 6 0 5 5.3 CCCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL303380 102292 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 391 6 0 5 5.3 CCCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
3533 1206 24 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1016/j.bmcl.2008.07.063
5282340 1206 24 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1016/j.bmcl.2008.07.063
CHEMBL291657 1206 24 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1016/j.bmcl.2008.07.063
42618174 193334 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 385 8 1 8 2.8 COCC(COC)Nc1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2008.07.063
CHEMBL524616 193334 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 385 8 1 8 2.8 COCC(COC)Nc1nc(C)nc2c(-c3ccc(OC)cc3C)c(C)nn12 10.1016/j.bmcl.2008.07.063
44587375 193400 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 393 9 0 6 4.8 CCCN(CCC)c1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL525716 193400 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 393 9 0 6 4.8 CCCN(CCC)c1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
10028059 102886 0 None - 1 Human 8.7 pKi = 8.7 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 476 7 1 4 6.9 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1Br 10.1021/jm960149e
CHEMBL305900 102886 0 None - 1 Human 8.7 pKi = 8.7 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 476 7 1 4 6.9 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1Br 10.1021/jm960149e
176157 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm049339c
3512 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm049339c
CHEMBL45281 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1021/jm049339c
44341581 9991 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 432 9 0 4 7.1 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(CC)c12 10.1016/s0960-894x(03)00621-8
CHEMBL114861 9991 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 432 9 0 4 7.1 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(CC)c12 10.1016/s0960-894x(03)00621-8
44341877 110465 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 412 8 0 4 6.6 CCCCN(CCCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL324728 110465 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 412 8 0 4 6.6 CCCCN(CCCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
127033261 138474 0 None 1 2 Human 8.7 pKi = 8.7 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3992 134 55 49 -7.3 CCCCCCCCCCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
CHEMBL3774713 138474 0 None 1 2 Human 8.7 pKi = 8.7 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3992 134 55 49 -7.3 CCCCCCCCCCCCCC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(CCCC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(CCCC)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC)NC(=O)C(C)(C)NC(=O)[C@H](C)NC1=O)C(C)C)[C@@H](C)O 10.1021/acs.jmedchem.5b00926
10739593 58995 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 397 8 0 6 5.6 CCCCN(CC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1SC 10.1021/jm980224g
CHEMBL169010 58995 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 397 8 0 6 5.6 CCCCN(CC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1SC 10.1021/jm980224g
44342074 9940 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 372 6 0 2 6.8 CCCN(CC1CC1)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL114596 9940 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 372 6 0 2 6.8 CCCN(CC1CC1)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
22249054 64007 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 397 8 1 5 5.3 CCc1nc(NC(CC)CC)c(OC)nc1-c1ccc(OC)cc1C(F)(F)F 10.1021/jm200365y
CHEMBL1807051 64007 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 397 8 1 5 5.3 CCc1nc(NC(CC)CC)c(OC)nc1-c1ccc(OC)cc1C(F)(F)F 10.1021/jm200365y
11291949 127509 0 None - 1 Human 8.7 pKi = 8.7 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3C)c(C)nn12 10.1021/jm040058e
CHEMBL366155 127509 0 None - 1 Human 8.7 pKi = 8.7 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3C)c(C)nn12 10.1021/jm040058e
44375151 56658 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 390 6 0 4 5.9 CCCN(CC1CC1)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(00)00071-8
CHEMBL164206 56658 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 390 6 0 4 5.9 CCCN(CC1CC1)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(00)00071-8
9801874 102972 1 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 412 7 1 4 6.4 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm960149e
CHEMBL306482 102972 1 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 412 7 1 4 6.4 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm960149e
9801874 102972 1 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 412 7 1 4 6.4 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm9900117
CHEMBL306482 102972 1 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 412 7 1 4 6.4 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm9900117
11247393 66813 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 6 0 6 5.1 CCN(Cc1ccc(C)cc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL186033 66813 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 6 0 6 5.1 CCN(Cc1ccc(C)cc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
44347137 14935 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 394 8 0 6 4.7 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL120823 14935 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 394 8 0 6 4.7 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
44347202 113514 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 364 7 0 5 4.6 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(OC)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL332101 113514 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 364 7 0 5 4.6 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(OC)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
9950788 110516 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 360 6 0 2 6.8 CCCCN(CC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL325047 110516 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 360 6 0 2 6.8 CCCCN(CC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
10095518 4379 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 454 6 0 5 6.4 CCN(c1nc(C)cc(-c2ccccc2[N+](=O)[O-])n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10125 4379 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 454 6 0 5 6.4 CCN(c1nc(C)cc(-c2ccccc2[N+](=O)[O-])n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
10027220 66865 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 458 7 1 4 6.0 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL186252 66865 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 458 7 1 4 6.0 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
122193720 123961 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 508 6 0 4 5.7 CCCCN(CC)c1cc(C)nc2c1N(C)C(=O)CN2c1ccc(Br)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628740 123961 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 508 6 0 4 5.7 CCCCN(CC)c1cc(C)nc2c1N(C)C(=O)CN2c1ccc(Br)cc1Br 10.1016/j.bmcl.2015.10.010
11430299 66732 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 6 0 6 5.1 CCN(Cc1cccc(C)c1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL185705 66732 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 6 0 6 5.1 CCN(Cc1cccc(C)c1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
11224120 123301 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 6 0 6 5.1 CCN(Cc1ccccc1C)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL361509 123301 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 6 0 6 5.1 CCN(Cc1ccccc1C)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
44341874 9918 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 412 6 0 2 7.5 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)ccc12 10.1016/s0960-894x(03)00684-x
CHEMBL114422 9918 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 412 6 0 2 7.5 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)ccc12 10.1016/s0960-894x(03)00684-x
177990 426 23 None 1 2 Rat 8.6 pKi = 8.6 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/s0960-894x(00)00071-8
3489 426 23 None 1 2 Rat 8.6 pKi = 8.6 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/s0960-894x(00)00071-8
CHEMBL296641 426 23 None 1 2 Rat 8.6 pKi = 8.6 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1016/s0960-894x(00)00071-8
15490822 98266 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 481 5 0 4 7.1 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(SC)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL274578 98266 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 481 5 0 4 7.1 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(SC)cc1Br 10.1016/s0960-894x(99)00132-8
90231885 123951 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 444 7 1 4 5.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Br)cc1CC 10.1016/j.bmcl.2015.10.010
CHEMBL3628729 123951 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 444 7 1 4 5.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Br)cc1CC 10.1016/j.bmcl.2015.10.010
90231897 123952 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 450 6 1 4 5.5 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628730 123952 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 450 6 1 4 5.5 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Br 10.1016/j.bmcl.2015.10.010
22249128 64015 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 9 1 5 5.6 CCc1nc(-c2ccc(OC(F)F)cc2Cl)c(OC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1807059 64015 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 399 9 1 5 5.6 CCc1nc(-c2ccc(OC(F)F)cc2Cl)c(OC)nc1NC(CC)CC 10.1021/jm200365y
10787254 204885 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 400 7 1 4 6.4 CCCN(CCC)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm960149e
CHEMBL75859 204885 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 400 7 1 4 6.4 CCCN(CCC)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm960149e
10787254 204885 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 400 7 1 4 6.4 CCCN(CCC)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm9900117
CHEMBL75859 204885 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 400 7 1 4 6.4 CCCN(CCC)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1C 10.1021/jm9900117
11465828 66762 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 482 6 0 6 6.1 CCN(Cc1ccc(Cl)c(Cl)c1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL185858 66762 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 482 6 0 6 6.1 CCN(Cc1ccc(Cl)c(Cl)c1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
177990 426 23 None -1 2 Human 8.6 pKi = 8.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm049085v
3489 426 23 None -1 2 Human 8.6 pKi = 8.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm049085v
CHEMBL296641 426 23 None -1 2 Human 8.6 pKi = 8.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm049085v
44347046 114545 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 377 6 0 3 6.5 CCCCN(CC)c1cc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2004.05.056
CHEMBL333713 114545 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 377 6 0 3 6.5 CCCCN(CC)c1cc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2004.05.056
44347046 114545 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 377 6 0 3 6.5 CCCCN(CC)c1cc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2004.05.019
CHEMBL333713 114545 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 377 6 0 3 6.5 CCCCN(CC)c1cc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2004.05.019
3520 3267 54 None 1 2 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2015.10.010
9821250 3267 54 None 1 2 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2015.10.010
CHEMBL309138 3267 54 None 1 2 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2015.10.010
11773421 66088 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCCN(CC)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL183845 66088 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCCN(CC)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
11326815 67561 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 392 7 0 6 4.4 CCCN(CC1CC1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL189821 67561 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 392 7 0 6 4.4 CCCN(CC1CC1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
3495 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity against [125I]-Try0-o-Corticotropin-releasing Factor to Corticotropin releasing hormone receptor 1 from ovineBinding affinity against [125I]-Try0-o-Corticotropin-releasing Factor to Corticotropin releasing hormone receptor 1 from ovine
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm960861b
5311055 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity against [125I]-Try0-o-Corticotropin-releasing Factor to Corticotropin releasing hormone receptor 1 from ovineBinding affinity against [125I]-Try0-o-Corticotropin-releasing Factor to Corticotropin releasing hormone receptor 1 from ovine
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm960861b
CHEMBL9946 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity against [125I]-Try0-o-Corticotropin-releasing Factor to Corticotropin releasing hormone receptor 1 from ovineBinding affinity against [125I]-Try0-o-Corticotropin-releasing Factor to Corticotropin releasing hormone receptor 1 from ovine
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm960861b
176157 2738 28 None 9 2 Human 8.6 pKi = 8.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2004.05.072
3512 2738 28 None 9 2 Human 8.6 pKi = 8.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2004.05.072
CHEMBL45281 2738 28 None 9 2 Human 8.6 pKi = 8.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2004.05.072
3495 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(99)00132-8
5311055 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(99)00132-8
CHEMBL9946 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(99)00132-8
3495 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2005.05.117
5311055 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2005.05.117
CHEMBL9946 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2005.05.117
90231888 123953 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 450 6 1 4 5.5 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Br)cc1Cl 10.1016/j.bmcl.2015.10.010
CHEMBL3628731 123953 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 450 6 1 4 5.5 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Br)cc1Cl 10.1016/j.bmcl.2015.10.010
3495 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(02)00358-x
5311055 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(02)00358-x
CHEMBL9946 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(02)00358-x
3495 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2007.12.050
5311055 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2007.12.050
CHEMBL9946 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2007.12.050
11306178 78326 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCC[C@@H](c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
11306179 78326 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCC[C@@H](c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL2094063 78326 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCC[C@@H](c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL2109725 78326 0 None - 1 Human 8.6 pKi = 8.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCC[C@@H](c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
3495 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
binding affinity for human CRF1 receptor in IMR32 neuroblastoma cellsbinding affinity for human CRF1 receptor in IMR32 neuroblastoma cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm990590f
5311055 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
binding affinity for human CRF1 receptor in IMR32 neuroblastoma cellsbinding affinity for human CRF1 receptor in IMR32 neuroblastoma cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm990590f
CHEMBL9946 1175 28 None - 1 Human 8.6 pKi = 8.6 Binding
binding affinity for human CRF1 receptor in IMR32 neuroblastoma cellsbinding affinity for human CRF1 receptor in IMR32 neuroblastoma cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1021/jm990590f
10788803 57577 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 430 7 1 6 5.4 CCCC(CC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL166669 57577 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 430 7 1 6 5.4 CCCC(CC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341879 9886 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 398 8 0 4 6.3 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(C)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL114273 9886 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 398 8 0 4 6.3 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(C)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
44290322 101170 0 None - 1 Human 8.6 pKi = 8.6 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.
ChEMBL 382 8 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1021/jm990590f
CHEMBL295563 101170 0 None - 1 Human 8.6 pKi = 8.6 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.
ChEMBL 382 8 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1021/jm990590f
10646985 57827 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 444 8 0 5 6.4 CCCCC(CC)Oc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL167017 57827 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 444 8 0 5 6.4 CCCCC(CC)Oc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
11282181 67351 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 442 8 0 6 5.6 CCCCN(Cc1ccccc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL188566 67351 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 442 8 0 6 5.6 CCCCN(Cc1ccccc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
9802053 124194 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 416 6 0 4 6.4 CCCC(CCC)N1CCc2nn(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL363414 124194 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 416 6 0 4 6.4 CCCC(CCC)N1CCc2nn(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
176157 2738 28 None 9 2 Human 7.7 pKi = 7.7 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2003.08.055
3512 2738 28 None 9 2 Human 7.7 pKi = 7.7 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL45281 2738 28 None 9 2 Human 7.7 pKi = 7.7 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2003.08.055
11326483 67779 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 380 5 0 6 3.8 CCC(CC)N1CCn2c(=O)n(-c3ccc(OC)cc3C)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL190881 67779 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 380 5 0 6 3.8 CCC(CC)N1CCn2c(=O)n(-c3ccc(OC)cc3C)c3nc(C)cc1c32 10.1021/jm050384+
21916279 165803 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 414 7 0 4 6.1 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL424812 165803 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 414 7 0 4 6.1 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
10810752 57499 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 396 7 0 6 4.3 CCN(CC)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
CHEMBL165991 57499 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 396 7 0 6 4.3 CCN(CC)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
10710543 58506 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 316 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1ccc(N(C)C)cc1SC 10.1021/jm980222w
CHEMBL168360 58506 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 316 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1ccc(N(C)C)cc1SC 10.1021/jm980222w
176157 2738 28 None 9 2 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2005.05.117
3512 2738 28 None 9 2 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2005.05.117
CHEMBL45281 2738 28 None 9 2 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/j.bmcl.2005.05.117
44307747 203585 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1nc(C)nc2c(-c3c(Cl)cccc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL66831 203585 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1nc(C)nc2c(-c3c(Cl)cccc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
20780178 93799 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 435 6 0 5 5.9 CCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12)CC1CCC1 10.1016/j.bmcl.2007.01.008
CHEMBL247558 93799 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 435 6 0 5 5.9 CCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12)CC1CCC1 10.1016/j.bmcl.2007.01.008
11153216 125834 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)cnn12 10.1021/jm040058e
CHEMBL364828 125834 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)cnn12 10.1021/jm040058e
10504455 58724 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 466 6 0 6 4.7 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(Br)cc1Br 10.1021/jm980224g
CHEMBL168531 58724 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 466 6 0 6 4.7 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(Br)cc1Br 10.1021/jm980224g
15490823 98449 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 513 5 0 5 5.8 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(S(C)(=O)=O)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL275738 98449 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 513 5 0 5 5.8 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(S(C)(=O)=O)cc1Br 10.1016/s0960-894x(99)00132-8
10500190 58787 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 383 8 0 7 3.1 COCCN(CCOC)c1nc(C)nc2c1ncn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL168788 58787 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 383 8 0 7 3.1 COCCN(CCOC)c1nc(C)nc2c1ncn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
10736859 120331 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 354 6 0 7 2.9 CCN(CCOC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL352916 120331 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 354 6 0 7 2.9 CCN(CCOC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
136216702 78621 0 None -2 2 Rat 6.7 pKi = 6.7 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 428 3 4 7 2.7 NCCNC(=O)c1c2c(c3c4c(ncnc14)-c1ccccc1C3=O)N[C@H]1CCCC[C@@H]1N2 10.1016/s0960-894x(99)00075-x
CHEMBL2112326 78621 0 None -2 2 Rat 6.7 pKi = 6.7 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 428 3 4 7 2.7 NCCNC(=O)c1c2c(c3c4c(ncnc14)-c1ccccc1C3=O)N[C@H]1CCCC[C@@H]1N2 10.1016/s0960-894x(99)00075-x
11222924 67601 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 386 5 0 6 3.7 CCCC(OC)N1CCn2c(=O)n(-c3ccc(Cl)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL190262 67601 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 386 5 0 6 3.7 CCCC(OC)N1CCn2c(=O)n(-c3ccc(Cl)cc3)c3nc(C)cc1c32 10.1021/jm050384+
44392772 122979 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 351 7 0 4 4.6 CCCN(CC1CC1)c1cc(C(=O)c2c(C)cc(C)cc2C)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL360845 122979 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 351 7 0 4 4.6 CCCN(CC1CC1)c1cc(C(=O)c2c(C)cc(C)cc2C)nc(C)n1 10.1016/j.bmcl.2004.05.072
44305974 102845 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 425 9 0 7 5.1 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C1(c2ccsc2)CC1 10.1016/j.bmcl.2004.02.053
CHEMBL305583 102845 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 425 9 0 7 5.1 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C1(c2ccsc2)CC1 10.1016/j.bmcl.2004.02.053
10761294 120395 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 364 2 0 5 4.1 Cc1cc(C)c(-n2c(C)c(C)c3c(N4CCOCC4)nc(C)nc32)c(C)c1 10.1021/jm980224g
CHEMBL353425 120395 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 364 2 0 5 4.1 Cc1cc(C)c(-n2c(C)c(C)c3c(N4CCOCC4)nc(C)nc32)c(C)c1 10.1021/jm980224g
9980256 94417 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 7 1 7 4.7 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC(C)=O 10.1016/j.bmcl.2007.09.008
CHEMBL251034 94417 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 7 1 7 4.7 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC(C)=O 10.1016/j.bmcl.2007.09.008
10551475 120778 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 448 9 0 8 3.2 COCCN(CCOC)c1ncnc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL355394 120778 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 448 9 0 8 3.2 COCCN(CCOC)c1ncnc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44317962 205627 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 462 7 1 3 6.5 O=C(CCc1ccncc1)C(Nc1ccc(Cl)cc1Cl)c1ccccc1Br 10.1021/jm049974i
CHEMBL81726 205627 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 462 7 1 3 6.5 O=C(CCc1ccncc1)C(Nc1ccc(Cl)cc1Cl)c1ccccc1Br 10.1021/jm049974i
135884427 57175 0 None -3 2 Rat 5.7 pKi = 5.7 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 374 3 4 7 1.1 NCCNC(=O)c1c2c(c3c(O)c4ccccc4c4ncnc1c34)=NCCN2 10.1016/s0960-894x(99)00075-x
CHEMBL164829 57175 0 None -3 2 Rat 5.7 pKi = 5.7 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 374 3 4 7 1.1 NCCNC(=O)c1c2c(c3c(O)c4ccccc4c4ncnc1c34)=NCCN2 10.1016/s0960-894x(99)00075-x
44318122 205828 0 None - 1 Human 7.7 pKi = 7.7 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 371 8 0 5 4.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL83385 205828 0 None - 1 Human 7.7 pKi = 7.7 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 371 8 0 5 4.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
44352382 116728 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 475 8 1 4 6.9 CCCN(Cc1sc(Nc2c(C)cc(C)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL337409 116728 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 475 8 1 4 6.9 CCCN(Cc1sc(Nc2c(C)cc(C)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
21916208 67339 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 428 8 0 4 6.4 CCCN(Cc1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL188523 67339 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 428 8 0 4 6.4 CCCN(Cc1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
10717814 120347 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 436 10 0 10 2.3 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL353050 120347 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 436 10 0 10 2.3 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
10254503 9732 0 None - 1 Rat 7.7 pKi = 7.7 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL 476 7 1 4 6.9 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Br)cc2Cl)c1Cl 10.1016/s0960-894x(00)00661-2
CHEMBL113333 9732 0 None - 1 Rat 7.7 pKi = 7.7 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL 476 7 1 4 6.9 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Br)cc2Cl)c1Cl 10.1016/s0960-894x(00)00661-2
21916260 6591 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 502 8 0 4 7.2 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1083102 6591 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 502 8 0 4 7.2 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
21916302 7664 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 448 7 0 4 6.4 CCCN(Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C)CC1CCC1 10.1016/j.bmcl.2010.01.127
CHEMBL1088478 7664 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 448 7 0 4 6.4 CCCN(Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C)CC1CCC1 10.1016/j.bmcl.2010.01.127
44446720 94779 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 366 6 0 2 6.8 CCCN(CCC)c1c(C)nc(-c2ccc(Cl)cc2C)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253287 94779 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 366 6 0 2 6.8 CCCN(CCC)c1c(C)nc(-c2ccc(Cl)cc2C)c2ccccc12 10.1016/j.bmcl.2007.12.050
11393576 123794 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 337 6 0 5 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ccc(C)nc3)c(C)nn12 10.1021/jm040058e
CHEMBL362305 123794 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 337 6 0 5 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ccc(C)nc3)c(C)nn12 10.1021/jm040058e
10552046 120791 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 462 8 0 8 3.5 COCC(COC)N(C)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL355494 120791 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 462 8 0 8 3.5 COCC(COC)N(C)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
122193727 123967 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 476 7 0 4 5.6 Cc1cc(N(C)C)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2CCCCF 10.1016/j.bmcl.2015.10.010
CHEMBL3628746 123967 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 476 7 0 4 5.6 Cc1cc(N(C)C)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2CCCCF 10.1016/j.bmcl.2015.10.010
11795486 120413 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 403 6 1 6 4.1 COCCNc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL353662 120413 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 403 6 1 6 4.1 COCCNc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44315264 205090 0 None - 1 Human 5.7 pKi = 5.7 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 361 6 1 5 4.5 Cc1cc(C)c(Nc2nc(C)nc(N(C)CCc3ccccc3)n2)c(C)c1 10.1021/jm960148m
CHEMBL77527 205090 0 None - 1 Human 5.7 pKi = 5.7 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 361 6 1 5 4.5 Cc1cc(C)c(Nc2nc(C)nc(N(C)CCc3ccccc3)n2)c(C)c1 10.1021/jm960148m
44315264 205090 0 None - 1 Human 5.7 pKi = 5.7 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 361 6 1 5 4.5 Cc1cc(C)c(Nc2nc(C)nc(N(C)CCc3ccccc3)n2)c(C)c1 10.1021/jm9900117
CHEMBL77527 205090 0 None - 1 Human 5.7 pKi = 5.7 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 361 6 1 5 4.5 Cc1cc(C)c(Nc2nc(C)nc(N(C)CCc3ccccc3)n2)c(C)c1 10.1021/jm9900117
44443597 93991 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 348 6 1 5 5.2 CCC(Nc1nc(C)c(Oc2cc(C)ccn2)nc1C)c1ccccc1 10.1016/j.bmcl.2007.09.008
CHEMBL248623 93991 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 348 6 1 5 5.2 CCC(Nc1nc(C)c(Oc2cc(C)ccn2)nc1C)c1ccccc1 10.1016/j.bmcl.2007.09.008
44443649 154407 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 430 8 1 6 5.4 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC1CC1 10.1016/j.bmcl.2007.09.008
CHEMBL398843 154407 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 430 8 1 6 5.4 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC1CC1 10.1016/j.bmcl.2007.09.008
44446734 155607 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 431 8 0 4 6.1 CCCN(CCN1CCCC1)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL404558 155607 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 431 8 0 4 6.1 CCCN(CCN1CCCC1)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
1799074 203777 3 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 301 4 2 3 4.1 CC(=O)/C(=N\Nc1ccccc1C)Nc1cccc(Cl)c1 10.1021/jm025512y
CHEMBL68118 203777 3 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 301 4 2 3 4.1 CC(=O)/C(=N\Nc1ccccc1C)Nc1cccc(Cl)c1 10.1021/jm025512y
44305524 203411 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 392 6 0 5 5.5 CCCCN(OC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL65574 203411 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 392 6 0 5 5.5 CCCCN(OC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
11795560 57688 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 404 7 0 4 5.7 CCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL166890 57688 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 404 7 0 4 5.7 CCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10741540 58128 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 434 9 0 5 5.3 CCN(CCOC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL167737 58128 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 434 9 0 5 5.3 CCN(CCOC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10549990 168070 0 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 418 5 0 5 4.7 CCN(c1nc(C)cc(N2CCOCC2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
CHEMBL432496 168070 0 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 418 5 0 5 4.7 CCN(c1nc(C)cc(N2CCOCC2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
10766371 59362 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 459 11 0 7 5.8 CCCCc1nc2c(N(CC)CCCC)nc(C)nc2n1-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL170791 59362 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 459 11 0 7 5.8 CCCCc1nc2c(N(CC)CCCC)nc(C)nc2n1-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
10549990 168070 0 None 1 2 Rat 7.7 pKi = 7.7 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 418 5 0 5 4.7 CCN(c1nc(C)cc(N2CCOCC2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980223o
CHEMBL432496 168070 0 None 1 2 Rat 7.7 pKi = 7.7 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 418 5 0 5 4.7 CCN(c1nc(C)cc(N2CCOCC2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980223o
10048452 94029 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 8 1 6 5.5 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(C)cc(C)n2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL248785 94029 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 8 1 6 5.5 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(C)cc(C)n2)nc1CC 10.1016/j.bmcl.2007.09.008
9980267 94443 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 8 1 6 5.6 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC(C)C 10.1016/j.bmcl.2007.09.008
CHEMBL251200 94443 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 8 1 6 5.6 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC(C)C 10.1016/j.bmcl.2007.09.008
10133826 193335 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 371 9 0 5 5.0 CCCN(CCC)c1c(CC)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL524617 193335 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 371 9 0 5 5.0 CCCN(CCC)c1c(CC)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
11178282 106424 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 408 10 0 6 5.3 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL3085417 106424 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 408 10 0 6 5.3 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL3139571 106424 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 408 10 0 6 5.3 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2OC)n(C)n1 10.1021/jm049339c
44337305 5307 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 358 7 0 4 4.8 CCCN(c1nc(-c2ccc(Cl)cc2C)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL106675 5307 0 None - 1 Human 7.7 pKi = 7.7 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 358 7 0 4 4.8 CCCN(c1nc(-c2ccc(Cl)cc2C)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
44392681 64525 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 339 6 1 4 4.9 CCC(CC)Nc1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL181439 64525 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 339 6 1 4 4.9 CCC(CC)Nc1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
20780282 63783 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 380 6 0 4 4.5 CCCN(CC1CC1)C(=O)c1c(C)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL180178 63783 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 380 6 0 4 4.5 CCCN(CC1CC1)C(=O)c1c(C)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780038 65609 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 436 7 0 4 5.3 CCCN(CCC(F)(F)F)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL183348 65609 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 436 7 0 4 5.3 CCCN(CCC(F)(F)F)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780036 65986 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 444 8 0 4 5.6 CCCN(CCc1ccccc1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL183639 65986 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 444 8 0 4 5.6 CCCN(CCc1ccccc1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
44306534 203468 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 371 8 0 6 4.3 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C1CCCC1 10.1016/j.bmcl.2004.02.053
CHEMBL65979 203468 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 371 8 0 6 4.3 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C1CCCC1 10.1016/j.bmcl.2004.02.053
44337502 5389 0 None - 1 Human 5.7 pKi = 5.7 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 378 9 0 4 5.5 C=CCn1nc(N(CCC)C(C2CC2)C2CC2)nc1-c1c(C)cc(C)cc1C 10.1016/s0960-894x(01)00657-6
CHEMBL107091 5389 0 None - 1 Human 5.7 pKi = 5.7 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 378 9 0 4 5.5 C=CCn1nc(N(CCC)C(C2CC2)C2CC2)nc1-c1c(C)cc(C)cc1C 10.1016/s0960-894x(01)00657-6
44307772 169433 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 313 4 1 5 3.6 CC(=O)/C(=N\Nc1ccccc1C#N)Oc1ccc(Cl)cc1 10.1021/jm025512y
CHEMBL442559 169433 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 313 4 1 5 3.6 CC(=O)/C(=N\Nc1ccccc1C#N)Oc1ccc(Cl)cc1 10.1021/jm025512y
10782556 59287 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 328 2 0 2 5.2 Cc1ccc2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL170487 59287 0 None - 1 Rat 6.7 pKi = 6.7 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 328 2 0 2 5.2 Cc1ccc2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
44266524 162583 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 428 6 0 6 4.8 CCN(c1nc(C)cc(-c2ccccn2)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
CHEMBL416882 162583 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 428 6 0 6 4.8 CCN(c1nc(C)cc(-c2ccccn2)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
44443632 94481 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 404 7 1 6 4.8 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC 10.1016/j.bmcl.2007.09.008
CHEMBL251397 94481 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 404 7 1 6 4.8 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC 10.1016/j.bmcl.2007.09.008
18449326 63982 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 397 9 1 5 4.6 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(COC)COC 10.1021/jm200365y
CHEMBL1807022 63982 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 397 9 1 5 4.6 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(COC)COC 10.1021/jm200365y
10892583 203430 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 321 4 2 3 3.9 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1C(F)(F)F 10.1021/jm025512y
CHEMBL65721 203430 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 321 4 2 3 3.9 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1C(F)(F)F 10.1021/jm025512y
3623188 203971 1 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 301 4 2 3 3.9 CC(=O)/C(=N\c1cccc(Cl)c1)NNc1ccc(C)cc1 10.1021/jm025512y
CHEMBL69431 203971 1 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 301 4 2 3 3.9 CC(=O)/C(=N\c1cccc(Cl)c1)NNc1ccc(C)cc1 10.1021/jm025512y
44266453 98267 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 428 6 0 6 4.8 CCN(c1nc(C)cc(-c2cccnc2)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
CHEMBL274579 98267 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 428 6 0 6 4.8 CCN(c1nc(C)cc(-c2cccnc2)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
12967650 19923 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 431 8 1 4 6.8 CCCN(Cc1sc(Nc2c(C)cc(C)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL130265 19923 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 431 8 1 4 6.8 CCCN(Cc1sc(Nc2c(C)cc(C)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
11246568 133612 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 399 6 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(Cl)cn3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL371348 133612 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 399 6 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(Cl)cn3)c3nc(C)cc1c32 10.1021/jm050384+
15965420 66935 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 468 7 0 4 6.8 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL186628 66935 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 468 7 0 4 6.8 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
10808132 57436 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 355 8 0 5 4.9 CCCCN(CC)c1nc(C)nc(N(CC)c2c(C)cc(C)cc2C)n1 10.1021/jm980222w
CHEMBL165473 57436 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 355 8 0 5 4.9 CCCCN(CC)c1nc(C)nc(N(CC)c2c(C)cc(C)cc2C)n1 10.1021/jm980222w
44392766 65331 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3N(C)C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL182915 65331 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3N(C)C)c(C)nn12 10.1016/j.bmcl.2004.05.056
20780080 145098 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 427 7 0 5 5.5 Cc1cc(C)c(-n2c3ncccc3n3c(CN(CC4CC4)CC4CC4)c(C)nc23)c(C)c1 10.1016/j.bmcl.2007.01.008
CHEMBL391169 145098 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 427 7 0 5 5.5 Cc1cc(C)c(-n2c3ncccc3n3c(CN(CC4CC4)CC4CC4)c(C)nc23)c(C)c1 10.1016/j.bmcl.2007.01.008
10298158 64608 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 457 7 1 4 7.1 CCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
CHEMBL181718 64608 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 457 7 1 4 7.1 CCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
18691327 98191 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 427 5 0 3 6.6 CCN(c1nc(C)cc(-c2ccccc2F)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL274081 98191 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 427 5 0 3 6.6 CCN(c1nc(C)cc(-c2ccccc2F)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
10789842 58127 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 453 9 0 9 2.7 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(N(C)C)cc1C(F)(F)F 10.1021/jm980224g
CHEMBL167717 58127 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 453 9 0 9 2.7 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(N(C)C)cc1C(F)(F)F 10.1021/jm980224g
9945957 63945 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 341 8 1 4 5.2 CCc1nc(-c2ccc(C)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806733 63945 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 341 8 1 4 5.2 CCc1nc(-c2ccc(C)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
11797773 58662 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 449 11 0 9 3.3 COCCCN(CCOC)c1nc(C)nc2c1ncn2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL168459 58662 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 449 11 0 9 3.3 COCCCN(CCOC)c1nc(C)nc2c1ncn2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
9805117 64988 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 478 7 0 6 7.0 CCCCN(CC)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
CHEMBL18230 64988 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 478 7 0 6 7.0 CCCCN(CC)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
44341455 165140 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 322 6 0 4 4.6 CCCN(CCC)c1cc(C)nc2c(-c3ccccc3)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL422784 165140 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 322 6 0 4 4.6 CCCN(CCC)c1cc(C)nc2c(-c3ccccc3)n(C)nc12 10.1016/s0960-894x(03)00621-8
20780283 7328 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 408 7 0 4 5.2 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
CHEMBL1086163 7328 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 408 7 0 4 5.2 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
10528499 120390 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 473 7 1 7 4.1 CCCC(Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br)C(=O)N(C)C 10.1021/jm980224g
CHEMBL353393 120390 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 473 7 1 7 4.1 CCCC(Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br)C(=O)N(C)C 10.1021/jm980224g
18691332 208115 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 424 5 1 4 6.1 CCN(c1nc(C)cc(-c2ccccc2N)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL9795 208115 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 424 5 1 4 6.1 CCN(c1nc(C)cc(-c2ccccc2N)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
44443599 153880 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 362 6 1 5 5.4 Cc1ccnc(Oc2nc(C)c(NC(c3ccccc3)C(C)C)nc2C)c1 10.1016/j.bmcl.2007.09.008
CHEMBL398300 153880 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 362 6 1 5 5.4 Cc1ccnc(Oc2nc(C)c(NC(c3ccccc3)C(C)C)nc2C)c1 10.1016/j.bmcl.2007.09.008
10646364 57529 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 430 6 0 4 5.9 CCN(CC)c1cc(C)nc(N(CC)c2c(Cl)cc(Br)cc2Cl)n1 10.1021/jm980222w
CHEMBL166238 57529 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 430 6 0 4 5.9 CCN(CC)c1cc(C)nc(N(CC)c2c(Cl)cc(Br)cc2Cl)n1 10.1021/jm980222w
11797409 57839 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 440 7 0 6 4.0 CCN(CC)c1cc(C)nc(N(CC)c2ccc(S(C)(=O)=O)cc2Br)n1 10.1021/jm980222w
CHEMBL167171 57839 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 440 7 0 6 4.0 CCN(CC)c1cc(C)nc(N(CC)c2ccc(S(C)(=O)=O)cc2Br)n1 10.1021/jm980222w
10501643 57866 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 408 7 0 5 5.3 CCN(CC)c1cc(C)nc(N(CC)c2ccc(SC)cc2Br)n1 10.1021/jm980222w
CHEMBL167195 57866 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 408 7 0 5 5.3 CCN(CC)c1cc(C)nc(N(CC)c2ccc(SC)cc2Br)n1 10.1021/jm980222w
44347223 15255 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 352 7 0 5 4.6 CCCN(CCC)c1cc(C)nc2c(-c3cccc(OC)c3)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL121183 15255 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 352 7 0 5 4.6 CCCN(CCC)c1cc(C)nc2c(-c3cccc(OC)c3)c(C)nn12 10.1016/j.bmcl.2004.05.019
44341736 10213 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 362 4 0 4 5.1 CCCN(C)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL116003 10213 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 362 4 0 4 5.1 CCCN(C)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
15490815 4542 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 487 5 0 3 7.3 CCN(c1nc(C)cc(-c2ccccc2Br)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10237 4542 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 487 5 0 3 7.3 CCN(c1nc(C)cc(-c2ccccc2Br)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
20780276 123935 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 474 6 0 4 5.6 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1c(C)cc(Cl)cc1Cl 10.1016/j.bmcl.2005.05.117
CHEMBL362815 123935 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 474 6 0 4 5.6 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1c(C)cc(Cl)cc1Cl 10.1016/j.bmcl.2005.05.117
44307879 102271 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 349 4 1 5 4.5 CCCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL303272 102271 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 349 4 1 5 4.5 CCCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
11282946 63366 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 440 11 0 6 5.8 CCCCC(c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(OC)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL179540 63366 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 440 11 0 6 5.8 CCCCC(c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(OC)cc2OC)n(C)n1 10.1021/jm049339c
11351594 124763 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 458 8 0 7 5.2 CCCN(Cc1cccc(OC)c1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL364214 124763 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 458 8 0 7 5.2 CCCN(Cc1cccc(OC)c1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
10667729 59078 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 384 8 0 8 2.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL169576 59078 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 384 8 0 8 2.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
44266439 208380 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 466 5 0 4 7.1 CCN(c1nc(C)cc(-c2c(C)cc(C)nc2C)n1)c1c(C)cc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL9956 208380 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 466 5 0 4 7.1 CCN(c1nc(C)cc(-c2c(C)cc(C)nc2C)n1)c1c(C)cc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
20780041 125296 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 506 7 0 4 7.2 FC(F)(F)c1nc2n(-c3ccc(Cl)cc3Cl)c3ccccc3n2c1CN(CC1CC1)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL364537 125296 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 506 7 0 4 7.2 FC(F)(F)c1nc2n(-c3ccc(Cl)cc3Cl)c3ccccc3n2c1CN(CC1CC1)CC1CC1 10.1016/j.bmcl.2005.06.028
3533 1206 24 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1016/j.bmcl.2004.02.053
5282340 1206 24 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1016/j.bmcl.2004.02.053
CHEMBL291657 1206 24 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 10.1016/j.bmcl.2004.02.053
44305973 100549 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 433 10 0 6 5.5 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)[C@@H](c1ccccc1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL291419 100549 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 433 10 0 6 5.5 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)[C@@H](c1ccccc1)C1CC1 10.1016/j.bmcl.2004.02.053
18672262 62636 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 473 8 1 4 7.7 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC(C)C 10.1016/j.bmcl.2004.10.055
CHEMBL178375 62636 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 473 8 1 4 7.7 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC(C)C 10.1016/j.bmcl.2004.10.055
11751505 124658 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 458 7 0 6 5.2 CCCN(CCC)c1c(Br)c(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL364168 124658 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 458 7 0 6 5.2 CCCN(CCC)c1c(Br)c(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
10316753 60491 0 None - 1 Human 5.6 pKi = 5.6 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 364 7 1 3 5.2 CCCN(c1n[nH]c(-c2ccc(Cl)cc2Cl)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL175536 60491 0 None - 1 Human 5.6 pKi = 5.6 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 364 7 1 3 5.2 CCCN(c1n[nH]c(-c2ccc(Cl)cc2Cl)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
10692645 59097 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 404 6 1 7 3.5 COCCNc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169693 59097 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 404 6 1 7 3.5 COCCNc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44443602 94037 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 376 8 1 5 5.7 CCc1nc(Oc2ncccc2C)c(CC)nc1NC(CC)c1ccccc1 10.1016/j.bmcl.2007.09.008
CHEMBL248816 94037 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 376 8 1 5 5.7 CCc1nc(Oc2ncccc2C)c(CC)nc1NC(CC)c1ccccc1 10.1016/j.bmcl.2007.09.008
44460263 205325 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 378 7 1 3 5.7 Cc1ccc(N[C@@H](C(=O)CCc2ccncc2)c2ccccc2C)c(Cl)c1 10.1021/jm049974i
CHEMBL79502 205325 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 378 7 1 3 5.7 Cc1ccc(N[C@@H](C(=O)CCc2ccncc2)c2ccccc2C)c(Cl)c1 10.1021/jm049974i
21916075 7582 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 406 3 0 4 5.4 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN2CCCCC2)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1087805 7582 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 406 3 0 4 5.4 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN2CCCCC2)c(C)c1 10.1016/j.bmcl.2010.01.127
10801589 161962 0 None - 1 Rat 5.6 pKi = 5.6 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 264 2 0 2 4.8 Cc1cc(C)c2ccn(-c3ccc(C(C)C)cc3)c2n1 10.1021/jm980223o
CHEMBL415752 161962 0 None - 1 Rat 5.6 pKi = 5.6 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 264 2 0 2 4.8 Cc1cc(C)c2ccn(-c3ccc(C(C)C)cc3)c2n1 10.1021/jm980223o
20780184 67097 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 504 7 0 4 7.3 CCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL187362 67097 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 504 7 0 4 7.3 CCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
11452262 73382 0 None - 1 Rat 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 396 5 1 5 4.9 COc1cccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL201470 73382 0 None - 1 Rat 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 396 5 1 5 4.9 COc1cccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)c1 10.1016/j.bmcl.2005.10.097
10596146 57608 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 383 9 0 6 4.1 CCN(c1nc(C)nc(N(CCOC)CC2CC2)n1)c1c(C)cc(C)cc1C 10.1021/jm980222w
CHEMBL166807 57608 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 383 9 0 6 4.1 CCN(c1nc(C)nc(N(CCOC)CC2CC2)n1)c1c(C)cc(C)cc1C 10.1021/jm980222w
10504356 120732 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 464 11 0 6 4.9 CCN(c1nc(C)cc(N(CCOC)CCOC)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
CHEMBL354859 120732 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 464 11 0 6 4.9 CCN(c1nc(C)cc(N(CCOC)CCOC)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
44392767 66274 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 367 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL184694 66274 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 367 7 0 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.056
10807869 58775 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 351 6 0 5 4.7 CCCCN(CC)c1nc(C)nc2c1ncn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL168731 58775 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 351 6 0 5 4.7 CCCCN(CC)c1nc(C)nc2c1ncn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
44307653 102156 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 363 5 1 5 4.9 CCCCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL302589 102156 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 363 5 1 5 4.9 CCCCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
10119101 132408 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 525 8 1 4 8.4 CCCN(Cc1ccc(F)cc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL369734 132408 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 525 8 1 4 8.4 CCCN(Cc1ccc(F)cc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
11639847 127513 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 396 5 0 5 5.1 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3OC)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL366179 127513 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 396 5 0 5 5.1 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3OC)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
10788201 58999 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 418 6 2 7 3.6 CCC(CO)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169035 58999 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 418 6 2 7 3.6 CCC(CO)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10573217 120495 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 402 5 0 6 4.3 CCN(CC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL354398 120495 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 402 5 0 6 4.3 CCN(CC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
20780155 67365 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 518 8 0 4 7.7 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL188623 67365 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 518 8 0 4 7.7 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
44305986 102125 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 425 9 0 7 5.1 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C1(c2cccs2)CC1 10.1016/j.bmcl.2004.02.053
CHEMBL302396 102125 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 425 9 0 7 5.1 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C1(c2cccs2)CC1 10.1016/j.bmcl.2004.02.053
11236826 140991 0 None - 1 Rat 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 473 7 1 6 5.9 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCc3ccccn3)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL382347 140991 0 None - 1 Rat 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 473 7 1 6 5.9 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCc3ccccn3)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
44443592 154992 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 362 7 1 5 5.3 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(C)c1ccccc1 10.1016/j.bmcl.2007.09.008
CHEMBL401327 154992 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 362 7 1 5 5.3 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(C)c1ccccc1 10.1016/j.bmcl.2007.09.008
10668655 24806 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(Nc2cc(Cl)c(Cl)cc2Cl)nc(C)n1 10.1021/jm960149e
CHEMBL134475 24806 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(Nc2cc(Cl)c(Cl)cc2Cl)nc(C)n1 10.1021/jm960149e
10573027 205032 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(Nc2c(Cl)cc(Cl)cc2Cl)nc(C)n1 10.1021/jm9900117
CHEMBL77006 205032 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(Nc2c(Cl)cc(Cl)cc2Cl)nc(C)n1 10.1021/jm9900117
44386385 60068 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 382 6 0 7 3.4 CCCN(CCC)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)nc1C 10.1016/s0960-894x(99)00108-0
CHEMBL173780 60068 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 382 6 0 7 3.4 CCCN(CCC)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)nc1C 10.1016/s0960-894x(99)00108-0
20780137 67400 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 482 7 0 4 7.2 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CCC1 10.1016/j.bmcl.2005.06.028
CHEMBL188813 67400 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 482 7 0 4 7.2 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CCC1 10.1016/j.bmcl.2005.06.028
10667355 57455 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 377 5 0 4 5.1 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(C(C)C)cc1OC 10.1021/jm980222w
CHEMBL165589 57455 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 377 5 0 4 5.1 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(C(C)C)cc1OC 10.1021/jm980222w
10813479 57485 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 450 8 0 5 6.4 CCN(CC)c1cc(C)nc(N(CC)c2c(Br)cc(C(C)C)cc2SC)n1 10.1021/jm980222w
CHEMBL165873 57485 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 450 8 0 5 6.4 CCN(CC)c1cc(C)nc(N(CC)c2c(Br)cc(C(C)C)cc2SC)n1 10.1021/jm980222w
44392761 122344 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 385 10 0 6 4.0 CCCN(CC1CC1)c1cc(Cc2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL359925 122344 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 385 10 0 6 4.0 CCCN(CC1CC1)c1cc(Cc2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
9865133 163867 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 388 6 1 3 5.8 CCCN(CC1CC1)c1cc(C)[nH]c2c(-c3ccc(Cl)cc3Cl)nnc1-2 10.1016/s0960-894x(03)00621-8
CHEMBL420681 163867 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 388 6 1 3 5.8 CCCN(CC1CC1)c1cc(C)[nH]c2c(-c3ccc(Cl)cc3Cl)nnc1-2 10.1016/s0960-894x(03)00621-8
20780016 65176 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 498 6 0 4 5.4 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1c(C)cc(C)cc1Br 10.1016/j.bmcl.2005.05.117
CHEMBL182482 65176 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 498 6 0 4 5.4 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1c(C)cc(C)cc1Br 10.1016/j.bmcl.2005.05.117
53310277 63984 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 403 8 0 3 6.2 CCc1nc(N(CC2CC2)CC2CC2)c(CC)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
CHEMBL1807024 63984 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 403 8 0 3 6.2 CCc1nc(N(CC2CC2)CC2CC2)c(CC)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
20780089 167773 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 399 7 0 5 5.1 C=CCN(CC=C)Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL430391 167773 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 399 7 0 5 5.1 C=CCN(CC=C)Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
44446727 94835 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(OC)cc2C)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253700 94835 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(OC)cc2C)c2ccccc12 10.1016/j.bmcl.2007.12.050
10163122 64833 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 483 8 1 4 7.5 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN(CC1CC1)CC1CC1 10.1016/j.bmcl.2004.10.055
CHEMBL181980 64833 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 483 8 1 4 7.5 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN(CC1CC1)CC1CC1 10.1016/j.bmcl.2004.10.055
11350066 168273 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 398 8 0 5 5.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(CC)c1ccccc1 10.1021/jm049339c
CHEMBL433940 168273 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 398 8 0 5 5.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(CC)c1ccccc1 10.1021/jm049339c
11394728 5674 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 374 8 0 5 4.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL107786 5674 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 374 8 0 5 4.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
44385520 130206 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 523 8 0 7 5.0 COCCN(Cc1ccccc1)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL367920 130206 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 523 8 0 7 5.0 COCCN(Cc1ccccc1)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
44318102 206057 0 None - 1 Human 6.6 pKi = 6.6 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 399 10 0 6 4.3 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(CC2CC2)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL85363 206057 0 None - 1 Human 6.6 pKi = 6.6 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 399 10 0 6 4.3 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(CC2CC2)c1=O 10.1016/s0960-894x(03)00483-9
21916125 6707 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 7 0 4 7.3 CCCN(Cc1cccc(F)c1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1083613 6707 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 7 0 4 7.3 CCCN(Cc1cccc(F)c1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
11211248 66169 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 382 7 1 7 3.6 CCC(COC)Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL184284 66169 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 382 7 1 7 3.6 CCC(COC)Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
10292638 118066 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 371 7 1 4 5.4 CCCN(CC1CC1)C(=O)c1sc(Nc2c(C)cc(C)cc2C)nc1C 10.1016/j.bmcl.2003.08.055
CHEMBL340469 118066 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 371 7 1 4 5.4 CCCN(CC1CC1)C(=O)c1sc(Nc2c(C)cc(C)cc2C)nc1C 10.1016/j.bmcl.2003.08.055
11427630 63010 0 None - 1 Human 5.6 pKi = 5.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 334 7 0 5 3.8 CCCN(CC1CC1)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL178725 63010 0 None - 1 Human 5.6 pKi = 5.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 334 7 0 5 3.8 CCCN(CC1CC1)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
44337533 167869 0 None - 1 Human 5.6 pKi = 5.6 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 326 6 0 4 4.4 CCCN(CCC)c1nc(-c2ccc(Cl)cc2Cl)n(C)n1 10.1016/s0960-894x(01)00657-6
CHEMBL431067 167869 0 None - 1 Human 5.6 pKi = 5.6 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 326 6 0 4 4.4 CCCN(CCC)c1nc(-c2ccc(Cl)cc2Cl)n(C)n1 10.1016/s0960-894x(01)00657-6
44446736 94630 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 433 10 0 4 6.4 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN(C)C)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL252302 94630 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 433 10 0 4 6.4 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN(C)C)c2ccccc12 10.1016/j.bmcl.2007.12.050
44443627 154027 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 422 9 1 6 4.9 CCc1nc(Oc2ccccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1016/j.bmcl.2007.09.008
CHEMBL398425 154027 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 422 9 1 6 4.9 CCc1nc(Oc2ccccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1016/j.bmcl.2007.09.008
10599448 58835 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 444 7 0 6 4.4 CCN(CCN(C)C)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168846 58835 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 444 7 0 6 4.4 CCN(CCN(C)C)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
11351416 73914 0 None - 1 Rat 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 450 5 1 5 5.8 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OC(F)(F)F)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL201966 73914 0 None - 1 Rat 6.6 pKi = 6.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 450 5 1 5 5.8 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OC(F)(F)F)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
10835160 57437 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 405 7 0 5 4.6 CCN(CC)c1cc(C)nc(N(CC)c2ccc(N(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL165475 57437 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 405 7 0 5 4.6 CCN(CC)c1cc(C)nc(N(CC)c2ccc(N(C)C)cc2Br)n1 10.1021/jm980222w
10621342 120441 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 405 7 0 5 5.1 CCN(CC)c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL353890 120441 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 405 7 0 5 5.1 CCN(CC)c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
53309695 64000 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 337 5 1 3 5.7 CCC(CC)Nc1nc(C)c(-c2ccc(Cl)cc2Cl)nc1C 10.1021/jm200365y
CHEMBL1807040 64000 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 337 5 1 3 5.7 CCC(CC)Nc1nc(C)c(-c2ccc(Cl)cc2Cl)nc1C 10.1021/jm200365y
21916306 7677 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 488 6 0 4 6.5 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN(CC2CCC2)CC(F)(F)F)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1088624 7677 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 488 6 0 4 6.5 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN(CC2CCC2)CC(F)(F)F)c(C)c1 10.1016/j.bmcl.2010.01.127
10618927 59046 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 366 5 2 5 4.5 CCC(CO)Nc1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL169418 59046 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 366 5 2 5 4.5 CCC(CO)Nc1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1021/jm980224g
10784215 59772 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 352 6 0 6 4.1 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL172571 59772 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 352 6 0 6 4.1 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
44341476 10069 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 392 8 0 4 6.3 CCCCN(CCCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL115313 10069 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 392 8 0 4 6.3 CCCCN(CCCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)n(C)nc12 10.1016/s0960-894x(03)00621-8
10764399 59066 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 416 7 1 7 4.1 COCC(Cc1ccccc1)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL169538 59066 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 416 7 1 7 4.1 COCC(Cc1ccccc1)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
135958361 57188 0 None 3 2 Rat 6.6 pKi = 6.6 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 428 3 4 7 2.4 NCCNC(=O)c1c2c(c3c(O)c4ccccc4c4ncnc1c34)=N[C@H]1CCCC[C@H]1N2 10.1016/s0960-894x(99)00075-x
CHEMBL164931 57188 0 None 3 2 Rat 6.6 pKi = 6.6 Binding
Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1Antagonistic activity against [125I]-Tyr-ovine CRF binding to Corticotropin releasing factor receptor 1
ChEMBL 428 3 4 7 2.4 NCCNC(=O)c1c2c(c3c(O)c4ccccc4c4ncnc1c34)=N[C@H]1CCCC[C@H]1N2 10.1016/s0960-894x(99)00075-x
20780021 63922 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 512 7 0 4 5.9 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2005.05.117
CHEMBL180613 63922 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 512 7 0 4 5.9 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2005.05.117
20780256 64299 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 518 7 0 4 6.8 CCc1nc2n(c1C(=O)N(CCC(F)(F)F)Cc1ccc(Cl)cc1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL181053 64299 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 518 7 0 4 6.8 CCc1nc2n(c1C(=O)N(CCC(F)(F)F)Cc1ccc(Cl)cc1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780055 93952 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 444 5 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)Cc4cccnc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL248367 93952 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 444 5 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)Cc4cccnc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
44443577 93987 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 346 8 2 4 5.6 CCc1nc(NC(CC)CC)c(CC)nc1Nc1ccc(Cl)cc1 10.1016/j.bmcl.2007.09.008
CHEMBL248588 93987 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 346 8 2 4 5.6 CCc1nc(NC(CC)CC)c(CC)nc1Nc1ccc(Cl)cc1 10.1016/j.bmcl.2007.09.008
3568686 203065 8 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 287 4 2 3 3.8 CC(=O)/C(=N\Nc1ccccc1)Nc1cccc(Cl)c1 10.1021/jm025512y
CHEMBL63664 203065 8 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 287 4 2 3 3.8 CC(=O)/C(=N\Nc1ccccc1)Nc1cccc(Cl)c1 10.1021/jm025512y
44587453 189107 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 359 9 0 6 4.1 CCCN(CCC)c1c(C)nc(-c2c(OC)cccc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL510224 189107 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 359 9 0 6 4.1 CCCN(CCC)c1c(C)nc(-c2c(OC)cccc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
20780170 123852 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 490 6 0 4 7.2 CCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL362567 123852 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 490 6 0 4 7.2 CCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
44352478 20871 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 505 8 1 4 7.9 CCCN(Cc1sc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL131046 20871 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 505 8 1 4 7.9 CCCN(Cc1sc(Nc2c(Cl)cc(C(F)(F)F)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
44352464 21444 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 539 8 1 4 7.4 CCCN(Cc1sc(Nc2c(Br)cc(C)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL131533 21444 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 539 8 1 4 7.4 CCCN(Cc1sc(Nc2c(Br)cc(C)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
20780173 127171 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 454 6 0 4 6.5 CCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL365715 127171 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 454 6 0 4 6.5 CCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
10526864 57562 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 434 8 0 6 4.8 CCN(CC)c1cc(C)nc(N(CC)c2c(Br)cc(C(C)=O)cc2OC)n1 10.1021/jm980222w
CHEMBL166504 57562 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 434 8 0 6 4.8 CCN(CC)c1cc(C)nc(N(CC)c2c(Br)cc(C(C)=O)cc2OC)n1 10.1021/jm980222w
10740490 178683 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 413 3 0 4 5.1 Cc1cc(N2CCOCC2)c2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL46798 178683 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 413 3 0 4 5.1 Cc1cc(N2CCOCC2)c2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
21916258 6705 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 522 7 0 4 7.8 CCCN(Cc1ccc(Cl)cc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1083611 6705 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 522 7 0 4 7.8 CCCN(Cc1ccc(Cl)cc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
20780133 93687 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 471 7 0 5 6.7 CCCN(Cc1ccccc1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL246944 93687 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 471 7 0 5 6.7 CCCN(Cc1ccccc1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
20780060 93760 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 419 7 0 5 5.4 C=CCN(CC=C)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL247358 93760 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 419 7 0 5 5.4 C=CCN(CC=C)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
44446721 155507 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 362 7 0 3 6.2 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2C)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL404171 155507 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 362 7 0 3 6.2 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2C)c2ccccc12 10.1016/j.bmcl.2007.12.050
12967653 64729 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 521 9 1 4 8.3 CCCN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181884 64729 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 521 9 1 4 8.3 CCCN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
11394728 5674 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 374 8 0 5 4.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(C1CC1)C1CC1 10.1021/jm049339c
CHEMBL107786 5674 0 None - 1 Human 7.6 pKi = 7.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 374 8 0 5 4.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(C1CC1)C1CC1 10.1021/jm049339c
11798947 59134 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 480 10 0 10 2.4 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(Br)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL169861 59134 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 480 10 0 10 2.4 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(Br)cc(OC)cc1OC 10.1021/jm980224g
44388401 62997 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 394 11 0 6 5.3 CCCCC(CC)N(OCCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL178667 62997 0 None - 1 Human 6.6 pKi = 6.6 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 394 11 0 6 5.3 CCCCC(CC)N(OCCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
10180472 21944 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 419 7 1 4 6.4 CCCCN(CC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
CHEMBL132055 21944 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 419 7 1 4 6.4 CCCCN(CC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
20780057 152162 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 458 6 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)CCc4ccccn4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL396821 152162 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 458 6 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)CCc4ccccn4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
10598041 120312 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 416 7 0 6 4.7 CCCCN(CC)c1ncnc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL352784 120312 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 416 7 0 6 4.7 CCCCN(CC)c1ncnc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10811877 165708 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 416 5 0 4 5.8 CCN(c1nc(C)cc(N2CCCCC2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
CHEMBL424562 165708 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 416 5 0 4 5.8 CCN(c1nc(C)cc(N2CCCCC2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
10665582 120409 1 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 350 5 1 4 5.5 CCCCNc1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL353638 120409 1 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 350 5 1 4 5.5 CCCCNc1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1021/jm980224g
44347190 15282 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 384 8 1 7 3.2 CCCN(CCO)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL121301 15282 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 384 8 1 7 3.2 CCCN(CCO)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
10548172 59128 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 385 3 0 5 4.3 COc1cc(Br)c(-n2cc(C#N)c3c(C)cc(C)nc32)c(OC)c1 10.1021/jm980223o
CHEMBL169838 59128 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 385 3 0 5 4.3 COc1cc(Br)c(-n2cc(C#N)c3c(C)cc(C)nc32)c(OC)c1 10.1021/jm980223o
44308157 203862 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 419 8 0 5 6.1 CCCCCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL68697 203862 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 419 8 0 5 6.1 CCCCCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
20780274 62993 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 382 7 0 4 4.8 CCCCN(CC)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL178617 62993 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 382 7 0 4 4.8 CCCCN(CC)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
10164483 122752 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 508 8 1 5 7.7 CCCN(Cc1cccnc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL360458 122752 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 508 8 1 5 7.7 CCCN(Cc1cccnc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
10183075 131450 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 459 8 1 4 7.5 CCCCN(CC)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL369109 131450 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 459 8 1 4 7.5 CCCCN(CC)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
44352437 21362 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 489 9 1 4 7.4 CCCN(Cc1sc(Nc2ccc(C(C)C)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL131422 21362 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 489 9 1 4 7.4 CCCN(Cc1sc(Nc2ccc(C(C)C)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
44441102 152165 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 409 6 1 5 5.5 CCCC(C)NCc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL396822 152165 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 409 6 1 5 5.5 CCCC(C)NCc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
44389083 62635 0 None - 1 Human 4.5 pKi = 4.5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 429 6 2 4 6.4 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CNCC1CC1 10.1016/j.bmcl.2004.10.055
CHEMBL178374 62635 0 None - 1 Human 4.5 pKi = 4.5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 429 6 2 4 6.4 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CNCC1CC1 10.1016/j.bmcl.2004.10.055
10914632 162686 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 335 4 2 3 4.3 CC(=O)/C(=N\c1cccc(C(F)(F)F)c1)NNc1ccccc1C 10.1021/jm025512y
CHEMBL417037 162686 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 335 4 2 3 4.3 CC(=O)/C(=N\c1cccc(C(F)(F)F)c1)NNc1ccccc1C 10.1021/jm025512y
44397564 67653 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 550 6 0 4 7.5 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC(F)(F)F)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL190638 67653 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 550 6 0 4 7.5 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC(F)(F)F)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
10549983 58874 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 418 7 1 7 3.9 COCCCNc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168883 58874 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 418 7 1 7 3.9 COCCCNc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
11022531 203788 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 287 4 2 3 3.6 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1Cl 10.1021/jm025512y
CHEMBL68238 203788 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 287 4 2 3 3.6 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1Cl 10.1021/jm025512y
CHEMBL413591 213076 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@@H](NC(C)=O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)N1)[C@@H](C)CC)C(N)=O 10.1021/jm034180+
10765122 58162 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 430 9 0 6 4.3 C=CCN(CC=C)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL168131 58162 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 430 9 0 6 4.3 C=CCN(CC=C)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2Br)n1 10.1021/jm980222w
44386432 59589 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 458 7 0 5 5.5 CCCCN(CC)c1cc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL171893 59589 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 458 7 0 5 5.5 CCCCN(CC)c1cc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
9955329 207830 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 448 8 0 8 3.9 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(Br)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL9633 207830 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 448 8 0 8 3.9 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(Br)cc(OC)cc1OC 10.1021/jm980224g
44340885 10159 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL None None None None 10.1016/s0960-894x(00)00661-2
CHEMBL115836 10159 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL None None None None 10.1016/s0960-894x(00)00661-2
44341765 9791 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 374 7 0 2 7.2 CCCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL113653 9791 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 374 7 0 2 7.2 CCCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
44342075 167873 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 360 6 0 2 6.8 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL431076 167873 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 360 6 0 2 6.8 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
44307478 102630 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cellsDisplacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cells
ChEMBL 423 8 0 7 3.7 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/j.bmc.2017.10.012
CHEMBL304272 102630 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cellsDisplacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cells
ChEMBL 423 8 0 7 3.7 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/j.bmc.2017.10.012
44307474 102638 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cellsDisplacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cells
ChEMBL 377 5 0 5 4.9 CCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/j.bmc.2017.10.012
CHEMBL304335 102638 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cellsDisplacement of 125I-sauvagine from CRF1 receptor in human IMR-32 cells
ChEMBL 377 5 0 5 4.9 CCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/j.bmc.2017.10.012
CHEMBL4299313 213565 0 None -2 2 Human 8.5 pKi = 8.5 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)(C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC(=O)C(CCCC)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(=O)CCOCCOCCOCCOCCOCCOCCN)[C@@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
3520 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from CRF1 receptor (unknown origin)Displacement of [125I]-Tyr0-sauvagine from CRF1 receptor (unknown origin)
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2015.10.010
9821250 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from CRF1 receptor (unknown origin)Displacement of [125I]-Tyr0-sauvagine from CRF1 receptor (unknown origin)
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2015.10.010
CHEMBL309138 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from CRF1 receptor (unknown origin)Displacement of [125I]-Tyr0-sauvagine from CRF1 receptor (unknown origin)
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2015.10.010
44307478 102630 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 423 8 0 7 3.7 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL304272 102630 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 423 8 0 7 3.7 COCCN(CCOC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
44307474 102638 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 377 5 0 5 4.9 CCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL304335 102638 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 377 5 0 5 4.9 CCCN(CC)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
44307892 203477 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 379 7 0 5 5.4 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)n(CC)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL66054 203477 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 379 7 0 5 5.4 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)n(CC)nc12 10.1016/s0960-894x(02)00358-x
9885480 203512 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 365 6 0 5 4.9 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL66275 203512 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 365 6 0 5 4.9 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)n(C)nc12 10.1016/s0960-894x(02)00358-x
3495 1175 28 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2008.07.063
5311055 1175 28 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2008.07.063
CHEMBL9946 1175 28 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2008.07.063
3520 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2008.07.063
9821250 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2008.07.063
CHEMBL309138 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/j.bmcl.2008.07.063
CHEMBL407570 212668 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC1CCCCC1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@@H](NC(C)=O)C(=O)N[C@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N1)[C@@H](C)CC)C(N)=O 10.1021/jm034180+
177990 426 23 None -1 2 Human 8.5 pKi = 8.5 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm050384+
3489 426 23 None -1 2 Human 8.5 pKi = 8.5 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm050384+
CHEMBL296641 426 23 None -1 2 Human 8.5 pKi = 8.5 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm050384+
10694630 59161 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 444 8 1 6 5.8 CCCCC(CC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169952 59161 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 444 8 1 6 5.8 CCCCC(CC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
9912938 4463 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 5 0 3 7.5 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10175 4463 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 5 0 3 7.5 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
122193723 123964 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 458 7 1 4 6.0 CCCN(CCC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628743 123964 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 458 7 1 4 6.0 CCCN(CCC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
177990 426 23 None -1 2 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm050070m
3489 426 23 None -1 2 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm050070m
CHEMBL296641 426 23 None -1 2 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 10.1021/jm050070m
11025 2740 7 None 1 2 Human 8.5 pKi = 8.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 10.1021/jm049085v
11713007 2740 7 None 1 2 Human 8.5 pKi = 8.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 10.1021/jm049085v
CHEMBL380800 2740 7 None 1 2 Human 8.5 pKi = 8.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 10.1021/jm049085v
44392707 63758 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 407 7 0 6 4.6 CCCN(CCOC)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL180142 63758 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 407 7 0 6 4.6 CCCN(CCOC)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
44392688 66315 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL184930 66315 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 391 6 0 5 5.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
10622522 59449 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 7 0 5 5.6 CCCCN(CC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL171202 59449 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 7 0 5 5.6 CCCCN(CC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44342014 9543 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 392 6 0 5 4.7 CCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112290 9543 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 392 6 0 5 4.7 CCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
44341754 10034 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 408 6 0 2 7.6 CCCN(Cc1ccccc1)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL115099 10034 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 408 6 0 2 7.6 CCCN(Cc1ccccc1)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
11774042 203352 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL65078 203352 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 402 6 0 4 5.9 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
9960282 64324 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 595 8 1 4 9.5 FC(F)(F)CCN(Cc1ccc(Cl)cc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181134 64324 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 595 8 1 4 9.5 FC(F)(F)CCN(Cc1ccc(Cl)cc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
9952376 9873 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 390 6 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
CHEMBL114193 9873 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 390 6 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00621-8
9952376 9873 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 390 6 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL114193 9873 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 390 6 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9843355 11230 2 None - 1 Human 8.5 pKi = 8.5 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
CHEMBL1178813 11230 2 None - 1 Human 8.5 pKi = 8.5 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
CHEMBL44169 11230 2 None - 1 Human 8.5 pKi = 8.5 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor receptorCompound was tested for the binding affinity to human corticotropin releasing factor receptor
ChEMBL 389 7 1 7 4.0 COCC(COC)n1nnc2c(Nc3c(C)cc(C)cc3Cl)nc(C)cc21 10.1021/jm990590f
9865624 15544 12 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL121896 15544 12 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
11384238 66850 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 406 6 1 4 5.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl 10.1016/j.bmcl.2015.10.010
CHEMBL186203 66850 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 406 6 1 4 5.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1Cl 10.1016/j.bmcl.2015.10.010
122193716 123954 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 478 6 1 4 5.0 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(I)cc1C 10.1016/j.bmcl.2015.10.010
CHEMBL3628732 123954 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 478 6 1 4 5.0 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(I)cc1C 10.1016/j.bmcl.2015.10.010
9865624 15544 12 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1021/jm040058e
CHEMBL121896 15544 12 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 398 9 0 7 3.9 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1021/jm040058e
11305029 66929 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 432 6 0 6 4.9 CCN(Cc1ccccc1F)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL186592 66929 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 432 6 0 6 4.9 CCN(Cc1ccccc1F)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
10789622 120739 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 447 8 0 7 4.5 CCCCN(CC)c1nc(C)nc2c1ncn2-c1c(Br)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL354940 120739 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 447 8 0 7 4.5 CCCCN(CC)c1nc(C)nc2c1ncn2-c1c(Br)cc(OC)cc1OC 10.1021/jm980224g
10835789 165322 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 417 8 0 7 4.7 CCCCN(CC)c1nc(C)nc2c1nc(C)n2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL423444 165322 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 417 8 0 7 4.7 CCCCN(CC)c1nc(C)nc2c1nc(C)n2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
10835759 168530 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 416 6 0 5 5.6 CCC(CC)Oc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL435468 168530 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 416 6 0 5 5.6 CCC(CC)Oc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44347236 113310 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 347 6 0 5 4.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(C#N)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL331539 113310 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 347 6 0 5 4.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(C#N)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
10363370 119875 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 396 7 0 4 5.8 CCN(CCCCF)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(00)00071-8
CHEMBL348967 119875 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 396 7 0 4 5.8 CCN(CCCCF)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(00)00071-8
CHEMBL4299313 213565 0 None -2 2 Human 8.5 pKi = 8.5 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)(C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC(=O)C(CCCC)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(=O)CCOCCOCCOCCOCCOCCOCCN)[C@@H](C)O)C(C)C)C(=O)N[C@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
3520 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm040058e
9821250 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm040058e
CHEMBL309138 3267 54 None 1 2 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm040058e
11189666 71195 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 395 6 0 3 6.6 CCCC(CCC)N1CCc2cn(-c3ccc(C)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL195631 71195 0 None - 1 Human 8.5 pKi = 8.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 395 6 0 3 6.6 CCCC(CCC)N1CCc2cn(-c3ccc(C)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
44381516 59049 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 443 8 1 5 6.4 CCCC(CCC)Nc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169430 59049 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 443 8 1 5 6.4 CCCC(CCC)Nc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44347217 96630 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 352 7 0 5 4.6 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL263492 96630 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 352 7 0 5 4.6 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
3495 1175 28 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2003.08.055
5311055 1175 28 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2003.08.055
CHEMBL9946 1175 28 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2003.08.055
9934089 5007 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 462 9 0 8 3.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL10504 5007 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 462 9 0 8 3.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341813 9603 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 416 6 0 4 6.1 Cc1cc(N(CC(C)C)CC2CC2)c2c(n1)c(-c1ccc(Cl)cc1Cl)nn2C 10.1016/s0960-894x(03)00622-x
CHEMBL112560 9603 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 416 6 0 4 6.1 Cc1cc(N(CC(C)C)CC2CC2)c2c(n1)c(-c1ccc(Cl)cc1Cl)nn2C 10.1016/s0960-894x(03)00622-x
9934089 5007 0 None - 1 Human 8.4 pKi = 8.4 Binding
Compound was tested for the inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneCompound was tested for the inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 462 9 0 8 3.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm990590f
CHEMBL10504 5007 0 None - 1 Human 8.4 pKi = 8.4 Binding
Compound was tested for the inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneCompound was tested for the inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 462 9 0 8 3.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm990590f
3495 1175 28 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2005.05.117
5311055 1175 28 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2005.05.117
CHEMBL9946 1175 28 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/j.bmcl.2005.05.117
18449330 63981 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 389 7 1 3 6.2 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(C1CC1)C1CC1 10.1021/jm200365y
CHEMBL1807021 63981 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 389 7 1 3 6.2 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(C1CC1)C1CC1 10.1021/jm200365y
10188470 131449 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 579 8 1 4 9.0 Fc1cccc(CN(CCC(F)(F)F)Cc2sc(Nc3c(Cl)cc(Cl)cc3Cl)nc2C(F)(F)F)c1 10.1016/j.bmcl.2004.10.055
CHEMBL369107 131449 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 579 8 1 4 9.0 Fc1cccc(CN(CCC(F)(F)F)Cc2sc(Nc3c(Cl)cc(Cl)cc3Cl)nc2C(F)(F)F)c1 10.1016/j.bmcl.2004.10.055
CHEMBL427807 213385 0 None -1 2 Human 8.4 pKi = 8.4 Binding
Binding affinity of the receptor corticotropin releasing factor receptor with peptidic agonistsBinding affinity of the receptor corticotropin releasing factor receptor with peptidic agonists
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H]1CCCN1C(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CC(=O)O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CO)C(=O)N[C@H](C(N)=O)C(C)C)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)O)[C@@H](C)O 10.1021/jm990590f
44341664 10025 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 434 6 0 2 7.9 CCCN(Cc1ccccc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL115030 10025 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 434 6 0 2 7.9 CCCN(Cc1ccccc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
3520 3267 54 None -1 2 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation counting
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm200365y
9821250 3267 54 None -1 2 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation counting
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm200365y
CHEMBL309138 3267 54 None -1 2 Rat 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation counting
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm200365y
10550438 205106 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 426 8 1 4 6.7 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1CC 10.1021/jm960149e
CHEMBL77716 205106 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 426 8 1 4 6.7 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1CC 10.1021/jm960149e
10550438 205106 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 426 8 1 4 6.7 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1CC 10.1021/jm9900117
CHEMBL77716 205106 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 426 8 1 4 6.7 CCCN(CC1CC1)c1nc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)c1CC 10.1021/jm9900117
44392702 156860 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 403 6 0 5 5.3 CCCN(CC1CC1)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL407168 156860 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 403 6 0 5 5.3 CCCN(CC1CC1)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
10670904 120750 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 442 7 0 4 6.6 CCCCN(CC)c1cc(C)nc2c1nc(C)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL355049 120750 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 442 7 0 4 6.6 CCCCN(CC)c1cc(C)nc2c1nc(C)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44347139 114948 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 368 7 1 6 4.6 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL334237 114948 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 368 7 1 6 4.6 CCC(CC)Nc1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
46872036 123955 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 366 6 1 4 4.7 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C)cc1C 10.1016/j.bmcl.2015.10.010
CHEMBL3628733 123955 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 366 6 1 4 4.7 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C)cc1C 10.1016/j.bmcl.2015.10.010
11628147 70560 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 434 4 0 4 6.1 CC[C@H]1Cn2nc(-c3ccc(C(F)(F)F)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL194836 70560 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 434 4 0 4 6.1 CC[C@H]1Cn2nc(-c3ccc(C(F)(F)F)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11605928 71896 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 396 5 0 5 5.1 CC[C@H]1Cn2nc(-c3ccc(OC)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL197134 71896 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 396 5 0 5 5.1 CC[C@H]1Cn2nc(-c3ccc(OC)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11560698 135280 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 414 5 0 4 6.1 CCC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL372653 135280 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 414 5 0 4 6.1 CCC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11598576 141348 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 388 4 0 4 5.7 CCC(CC)N1CCn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c32 10.1021/jm049085v
CHEMBL383602 141348 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 388 4 0 4 5.7 CCC(CC)N1CCn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c32 10.1021/jm049085v
11795560 57688 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 404 7 0 4 5.7 CCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL166890 57688 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 404 7 0 4 5.7 CCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
44375438 56560 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 408 7 0 4 5.8 Cc1cc(C)c(-n2c(C)c(C)c3c(N(CCCF)CC4CC4)nc(C)nc32)c(C)c1 10.1016/s0960-894x(00)00071-8
CHEMBL164042 56560 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Compound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellumCompound was tested in vitro for its ability to displace [125 I]Tyr-sauvagine from corticotropin-releasing hormone type 1 receptor in rat cerebellum
ChEMBL 408 7 0 4 5.8 Cc1cc(C)c(-n2c(C)c(C)c3c(N(CCCF)CC4CC4)nc(C)nc32)c(C)c1 10.1016/s0960-894x(00)00071-8
10048451 153832 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 9 1 6 5.6 CCCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(C)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL398258 153832 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 9 1 6 5.6 CCCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(C)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
44446740 155609 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 475 10 0 5 6.2 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCOCC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL404560 155609 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 475 10 0 5 6.2 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCOCC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
10573027 205032 0 None - 1 Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(Nc2c(Cl)cc(Cl)cc2Cl)nc(C)n1 10.1021/jm960149e
CHEMBL77006 205032 0 None - 1 Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(Nc2c(Cl)cc(Cl)cc2Cl)nc(C)n1 10.1021/jm960149e
10573027 205032 0 None - 1 Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(Nc2c(Cl)cc(Cl)cc2Cl)nc(C)n1 10.1021/jm9900117
CHEMBL77006 205032 0 None - 1 Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(Nc2c(Cl)cc(Cl)cc2Cl)nc(C)n1 10.1021/jm9900117
11152649 68521 0 None - 1 Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 361 6 0 3 6.0 CCCC(CCC)N1CCc2cn(-c3ccc(C)cc3)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL191755 68521 0 None - 1 Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 361 6 0 3 6.0 CCCC(CCC)N1CCc2cn(-c3ccc(C)cc3)c3nc(C)cc1c23 10.1021/jm050070m
20780290 63921 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 378 7 0 4 4.3 C=CCN(CC=C)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL180610 63921 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 378 7 0 4 4.3 C=CCN(CC=C)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780257 64287 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 464 7 0 4 6.2 CCCN(Cc1ccc(Cl)cc1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL181002 64287 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 464 7 0 4 6.2 CCCN(Cc1ccc(Cl)cc1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
11798634 57594 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 470 7 0 5 5.3 CCN(CC)c1cc(C)nc(N(CC)c2c(Br)cc(Br)cc2OC)n1 10.1021/jm980222w
CHEMBL166776 57594 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 470 7 0 5 5.3 CCN(CC)c1cc(C)nc(N(CC)c2c(Br)cc(Br)cc2OC)n1 10.1021/jm980222w
11792683 58099 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 357 8 0 6 3.7 CCN(CCOC)c1nc(C)nc(N(CC)c2c(C)cc(C)cc2C)n1 10.1021/jm980222w
CHEMBL167464 58099 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 357 8 0 6 3.7 CCN(CCOC)c1nc(C)nc(N(CC)c2c(C)cc(C)cc2C)n1 10.1021/jm980222w
44392760 65242 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 391 9 0 4 5.3 C=CCc1c(C(=O)c2c(C)cc(C)cc2C)nc(C)nc1N(CCC)CC1CC1 10.1016/j.bmcl.2004.05.072
CHEMBL182706 65242 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 391 9 0 4 5.3 C=CCc1c(C(=O)c2c(C)cc(C)cc2C)nc(C)nc1N(CCC)CC1CC1 10.1016/j.bmcl.2004.05.072
176157 2738 28 None -9 2 Rat 7.5 pKi = 7.5 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/s0960-894x(00)00661-2
3512 2738 28 None -9 2 Rat 7.5 pKi = 7.5 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/s0960-894x(00)00661-2
CHEMBL45281 2738 28 None -9 2 Rat 7.5 pKi = 7.5 Binding
Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.Binding affinity towards Corticotropin releasing hormone receptor type 1 of rat cerebellum using [125I]Tyr-sauvagine as radioligand.
ChEMBL 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 10.1016/s0960-894x(00)00661-2
21916078 7678 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 420 6 0 4 5.6 CCN(Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C)CC1CC1 10.1016/j.bmcl.2010.01.127
CHEMBL1088625 7678 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 420 6 0 4 5.6 CCN(Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C)CC1CC1 10.1016/j.bmcl.2010.01.127
44386496 62578 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 499 10 0 6 6.4 CCCCN(CC)c1nc(C)nc2c1nc(OCC1CC1)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL178272 62578 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 499 10 0 6 6.4 CCCCN(CC)c1nc(C)nc2c1nc(OCC1CC1)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
10648379 59077 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 479 10 0 9 3.0 COCCN(CCOC)c1nc(C)nc2c1ncn2-c1c(Br)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL169571 59077 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 479 10 0 9 3.0 COCCN(CCOC)c1nc(C)nc2c1ncn2-c1c(Br)cc(OC)cc1OC 10.1021/jm980224g
11501973 96846 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 388 4 0 4 5.7 CCCN1c2cc(C)nc3c(-c4ccc(Cl)cc4Cl)nn(c23)C[C@@H]1CC 10.1021/jm049085v
CHEMBL265282 96846 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 388 4 0 4 5.7 CCCN1c2cc(C)nc3c(-c4ccc(Cl)cc4Cl)nn(c23)C[C@@H]1CC 10.1021/jm049085v
22324325 205873 0 None - 1 Human 6.5 pKi = 6.5 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 373 9 0 6 3.9 CCCN(CCC)c1c(C)nc(-c2c(OC)cccc2OC)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL83789 205873 0 None - 1 Human 6.5 pKi = 6.5 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 373 9 0 6 3.9 CCCN(CCC)c1c(C)nc(-c2c(OC)cccc2OC)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
21916104 6418 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 426 6 0 4 6.0 CCCCN(C)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1082368 6418 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 426 6 0 4 6.0 CCCCN(C)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
16416344 203378 14 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 376 2 0 5 4.2 Cc1cc(N2CCOCC2)n2nc(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(98)00372-2
CHEMBL65308 203378 14 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 376 2 0 5 4.2 Cc1cc(N2CCOCC2)n2nc(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(98)00372-2
44337472 108951 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 366 8 0 4 5.3 CCCN(c1nc(-c2c(C)cc(C)cc2C)n(CC)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL321155 108951 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 366 8 0 4 5.3 CCCN(c1nc(-c2c(C)cc(C)cc2C)n(CC)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
10228046 21439 0 None - 1 Human 4.5 pKi = 4.5 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 485 7 1 4 7.1 CCCN(CC1CC1)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2003.08.055
CHEMBL131530 21439 0 None - 1 Human 4.5 pKi = 4.5 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 485 7 1 4 7.1 CCCN(CC1CC1)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2003.08.055
44460259 205635 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 398 7 1 3 6.1 Cc1ccccc1[C@H](Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
CHEMBL81760 205635 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 398 7 1 3 6.1 Cc1ccccc1[C@H](Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
9828535 165561 0 None 1 2 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980222w
CHEMBL424204 165561 0 None 1 2 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980222w
CHEMBL43216 165561 0 None 1 2 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980222w
44341728 9983 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 396 7 0 4 6.0 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(C)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL114821 9983 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 396 7 0 4 6.0 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(C)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
44341763 163434 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 404 7 0 4 6.4 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL419761 163434 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 404 7 0 4 6.4 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
9821153 9476 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 378 5 0 5 4.3 COCCN(C)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL111960 9476 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 378 5 0 5 4.3 COCCN(C)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
21916241 6489 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 456 8 0 5 5.6 CCCN(CCOC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1082685 6489 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 456 8 0 5 5.6 CCCN(CCOC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
11225236 141370 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 472 7 1 5 6.5 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCc3ccccc3)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL383773 141370 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 472 7 1 5 6.5 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCc3ccccc3)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
21916145 7500 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 434 7 0 4 6.0 CCCN(Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C)CC1CC1 10.1016/j.bmcl.2010.01.127
CHEMBL1087164 7500 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 434 7 0 4 6.0 CCCN(Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C)CC1CC1 10.1016/j.bmcl.2010.01.127
44446742 94679 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 489 10 1 5 6.3 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCCC(O)C2)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL252688 94679 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 489 10 1 5 6.3 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCCC(O)C2)c2ccccc12 10.1016/j.bmcl.2007.12.050
9828535 165561 0 None 1 2 Human 7.5 pKi = 7.5 Binding
Inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneInhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm990590f
CHEMBL424204 165561 0 None 1 2 Human 7.5 pKi = 7.5 Binding
Inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneInhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm990590f
CHEMBL43216 165561 0 None 1 2 Human 7.5 pKi = 7.5 Binding
Inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneInhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm990590f
10671608 58757 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 458 9 0 6 5.8 CCCCN(CCCC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168646 58757 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 458 9 0 6 5.8 CCCCN(CCCC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
11247120 10291 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL116167 10291 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 418 8 0 4 6.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
44341738 10041 1 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 332 6 0 2 6.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(C)cc3)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL115154 10041 1 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 332 6 0 2 6.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(C)cc3)cccc12 10.1016/s0960-894x(03)00684-x
44341729 10406 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 432 9 0 4 7.1 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL116280 10406 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 432 9 0 4 7.1 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
46891011 6437 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 3 0 4 6.0 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCC(C)CC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082444 6437 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 3 0 4 6.0 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCC(C)CC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
20780059 166602 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 458 6 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)CCc4ccncc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL428044 166602 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 458 6 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)CCc4ccncc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
44337516 7587 0 None - 1 Human 5.5 pKi = 5.5 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 338 7 1 3 4.8 CCCN(c1n[nH]c(-c2c(C)cc(C)cc2C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL108784 7587 0 None - 1 Human 5.5 pKi = 5.5 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 338 7 1 3 4.8 CCCN(c1n[nH]c(-c2c(C)cc(C)cc2C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
44317667 104413 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 406 8 1 3 6.5 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2C(C)C)c(Cl)c1 10.1021/jm049974i
CHEMBL310343 104413 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 406 8 1 3 6.5 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2C(C)C)c(Cl)c1 10.1021/jm049974i
10572455 57690 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 389 7 1 5 4.8 C=CCNc1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL166897 57690 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 389 7 1 5 4.8 C=CCNc1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
20780009 6626 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 466 6 0 4 6.0 CCCN(CC1CC1)C(=O)c1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1083299 6626 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 466 6 0 4 6.0 CCCN(CC1CC1)C(=O)c1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
44587490 188120 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 361 7 0 4 5.4 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1Cl 10.1016/j.bmcl.2008.07.063
CHEMBL498319 188120 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 361 7 0 4 5.4 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1Cl 10.1016/j.bmcl.2008.07.063
44337293 5311 0 None - 1 Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 344 7 0 4 4.5 CCCN(c1nc(-c2ccc(Cl)cc2)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL106728 5311 0 None - 1 Human 7.5 pKi = 7.5 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 344 7 0 4 4.5 CCCN(c1nc(-c2ccc(Cl)cc2)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
10791657 58725 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 504 9 0 9 3.3 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(OC(F)(F)F)cc1Br 10.1021/jm980224g
CHEMBL168536 58725 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 504 9 0 9 3.3 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(OC(F)(F)F)cc1Br 10.1021/jm980224g
10765120 58263 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 430 7 0 7 4.1 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(C(C)=O)cc1Br 10.1021/jm980224g
CHEMBL168252 58263 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 430 7 0 7 4.1 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(C(C)=O)cc1Br 10.1021/jm980224g
44460600 105127 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 412 8 1 3 6.3 CCc1ccccc1C(Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
CHEMBL311431 105127 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 412 8 1 3 6.3 CCc1ccccc1C(Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
46881383 7164 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 408 6 0 4 5.3 CCCN(CC1CCC1)C(=O)c1c(C)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
CHEMBL1085431 7164 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 408 6 0 4 5.3 CCCN(CC1CCC1)C(=O)c1c(C)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
10640801 58782 1 None - 1 Rat 5.5 pKi = 5.5 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 339 2 0 3 3.5 Cc1cc(C)nc(N(C)c2ccc(I)cc2)n1 10.1021/jm980222w
CHEMBL168764 58782 1 None - 1 Rat 5.5 pKi = 5.5 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 339 2 0 3 3.5 Cc1cc(C)nc(N(C)c2ccc(I)cc2)n1 10.1021/jm980222w
44397565 122636 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 580 9 0 4 8.5 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCc4ccccc4)CCc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL360389 122636 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 580 9 0 4 8.5 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCc4ccccc4)CCc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
44318056 205250 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity of compound towards human Corticotropin releasing factor receptor 1Binding affinity of compound towards human Corticotropin releasing factor receptor 1
ChEMBL 398 7 1 3 6.1 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2Cl)c(Cl)c1 10.1021/jm049974i
CHEMBL78884 205250 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity of compound towards human Corticotropin releasing factor receptor 1Binding affinity of compound towards human Corticotropin releasing factor receptor 1
ChEMBL 398 7 1 3 6.1 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2Cl)c(Cl)c1 10.1021/jm049974i
44443609 94155 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 420 10 1 6 5.7 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(COC(C)C)c1ccccc1 10.1016/j.bmcl.2007.09.008
CHEMBL249430 94155 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 420 10 1 6 5.7 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(COC(C)C)c1ccccc1 10.1016/j.bmcl.2007.09.008
44460599 168122 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 412 7 1 3 6.4 Cc1cccc(C)c1C(Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
CHEMBL432928 168122 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 412 7 1 3 6.4 Cc1cccc(C)c1C(Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
44443578 154849 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 327 8 2 5 4.6 CCc1nc(NC(CC)CC)c(CC)nc1Nc1cccc(C)n1 10.1016/j.bmcl.2007.09.008
CHEMBL400531 154849 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 327 8 2 5 4.6 CCc1nc(NC(CC)CC)c(CC)nc1Nc1cccc(C)n1 10.1016/j.bmcl.2007.09.008
20780184 67097 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 504 7 0 4 7.3 CCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL187362 67097 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 504 7 0 4 7.3 CCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
20780065 166375 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 558 7 0 4 7.6 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CC4CC4)CC(F)(F)C(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL427527 166375 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 558 7 0 4 7.6 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CC4CC4)CC(F)(F)C(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
44341855 114808 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 467 8 0 5 6.5 CCCCN(CCc1ccncc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL334061 114808 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 467 8 0 5 6.5 CCCCN(CCc1ccncc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
10502734 120446 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 429 3 0 3 6.8 Cc1cc(-c2ccccc2)c2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL353916 120446 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 429 3 0 3 6.8 Cc1cc(-c2ccccc2)c2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
20780265 6549 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 560 7 0 4 7.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)Cc4ccc(F)cc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082963 6549 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 560 7 0 4 7.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)Cc4ccc(F)cc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
11307122 73657 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 532 9 1 7 6.5 COc1cc(COc2ccc(S(=O)(=O)c3ccc(C)nc3Nc3c(C)cc(C)cc3C)cc2)cc(OC)c1 10.1016/j.bmcl.2005.10.097
CHEMBL201798 73657 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 532 9 1 7 6.5 COc1cc(COc2ccc(S(=O)(=O)c3ccc(C)nc3Nc3c(C)cc(C)cc3C)cc2)cc(OC)c1 10.1016/j.bmcl.2005.10.097
44341861 9600 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 384 8 0 4 6.0 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112549 9600 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 384 8 0 4 6.0 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)nn(C)c12 10.1016/s0960-894x(03)00622-x
20780288 5589 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 406 6 0 4 4.9 Cc1cc(C)c(N2CCCn3c2nc(C)c3C(=O)N(CC2CC2)CC2CC2)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1077158 5589 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 406 6 0 4 4.9 Cc1cc(C)c(N2CCCn3c2nc(C)c3C(=O)N(CC2CC2)CC2CC2)c(C)c1 10.1016/j.bmcl.2010.01.127
44337533 167869 0 None - 1 Human 5.5 pKi = 5.5 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 326 6 0 4 4.4 CCCN(CCC)c1nc(-c2ccc(Cl)cc2Cl)n(C)n1 10.1021/jm049339c
CHEMBL431067 167869 0 None - 1 Human 5.5 pKi = 5.5 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 326 6 0 4 4.4 CCCN(CCC)c1nc(-c2ccc(Cl)cc2Cl)n(C)n1 10.1021/jm049339c
44337577 5344 0 None - 1 Human 5.5 pKi = 5.5 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 390 6 0 5 5.3 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(C)n1)c1ccccc1OC 10.1016/s0960-894x(01)00657-6
CHEMBL106874 5344 0 None - 1 Human 5.5 pKi = 5.5 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 390 6 0 5 5.3 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(C)n1)c1ccccc1OC 10.1016/s0960-894x(01)00657-6
44386313 120826 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 514 8 0 7 5.5 CCCCN(CC)c1nc(C)nc2c1nc(N1CCOCC1)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL355803 120826 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 514 8 0 7 5.5 CCCCN(CC)c1nc(C)nc2c1nc(N1CCOCC1)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
10550837 57828 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 434 7 2 8 2.2 Cc1nc(N(CCO)CCO)c2nnn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980224g
CHEMBL167024 57828 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 434 7 2 8 2.2 Cc1nc(N(CCO)CCO)c2nnn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980224g
10041172 162463 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 311 4 2 3 3.6 C#Cc1cccc(/N=C(/NNc2ccccc2Cl)C(C)=O)c1 10.1021/jm025512y
CHEMBL416693 162463 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 311 4 2 3 3.6 C#Cc1cccc(/N=C(/NNc2ccccc2Cl)C(C)=O)c1 10.1021/jm025512y
10688248 58809 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 335 4 0 4 4.0 CCN(c1nc(C)cc(C)n1)c1ccc(OC)cc1Br 10.1021/jm980222w
CHEMBL168824 58809 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 335 4 0 4 4.0 CCN(c1nc(C)cc(C)n1)c1ccc(OC)cc1Br 10.1021/jm980222w
44341697 9946 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL114649 9946 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
10319873 94265 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(C)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL250282 94265 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(C)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
21916156 6895 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 7 0 4 7.3 CCCN(Cc1ccc(F)cc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1084297 6895 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 7 0 4 7.3 CCCN(Cc1ccc(F)cc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
21916243 6966 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 474 6 0 4 6.7 CCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1084564 6966 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 474 6 0 4 6.7 CCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
21916231 7411 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 542 7 0 4 7.3 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCc4ccccc4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1086522 7411 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 542 7 0 4 7.3 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCc4ccccc4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
11395654 78327 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 406 10 0 5 5.9 CCCC[C@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL2094064 78327 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 406 10 0 5 5.9 CCCC[C@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL2109726 78327 0 None - 1 Human 6.5 pKi = 6.5 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 406 10 0 5 5.9 CCCC[C@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
44352370 18883 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 455 8 1 4 7.0 CCCN(Cc1oc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL128310 18883 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 455 8 1 4 7.0 CCCN(Cc1oc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
18691315 98243 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 453 6 1 4 6.2 CCN(c1nc(C)cc(-c2ccccc2C(=O)O)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL274439 98243 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 453 6 1 4 6.2 CCN(c1nc(C)cc(-c2ccccc2C(=O)O)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
10268909 193556 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 341 7 0 4 5.0 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2C)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL526829 193556 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 341 7 0 4 5.0 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2C)nc1OC 10.1016/j.bmcl.2008.07.063
20780126 168251 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 482 6 0 4 6.5 CCCN(CC1CC1)C(=O)c1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL433763 168251 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 482 6 0 4 6.5 CCCN(CC1CC1)C(=O)c1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
10686839 58144 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 315 5 0 4 5.1 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1SC 10.1021/jm980222w
CHEMBL167871 58144 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 315 5 0 4 5.1 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1SC 10.1021/jm980222w
10787443 59035 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 404 3 0 2 6.9 Cc1cc(-c2ccccc2)c2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL169359 59035 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 404 3 0 2 6.9 Cc1cc(-c2ccccc2)c2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
20780122 93840 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 423 7 0 5 5.9 CCCCN(CC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL247755 93840 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 423 7 0 5 5.9 CCCCN(CC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
20780177 147004 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 421 6 0 5 5.5 CCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
CHEMBL392654 147004 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 421 6 0 5 5.5 CCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
44446722 94805 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 376 8 0 3 6.4 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2CC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253491 94805 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 376 8 0 3 6.4 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2CC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL2372911 210312 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N1)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm034180+
10838946 59064 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 494 8 1 7 5.1 COCC(Cc1ccccc1)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169528 59064 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 494 8 1 7 5.1 COCC(Cc1ccccc1)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
12967647 18941 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 431 7 1 4 6.4 CCCN(CC1CC1)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
CHEMBL128625 18941 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 431 7 1 4 6.4 CCCN(CC1CC1)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
20780124 67413 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 428 6 0 4 5.8 CCCN(CC1CC1)C(=O)c1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL188849 67413 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 428 6 0 4 5.8 CCCN(CC1CC1)C(=O)c1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
44392802 122179 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 395 10 1 4 5.2 CCCN(CC1CC1)c1cc(C(O)c2c(CC)cc(CC)cc2CC)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL359745 122179 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 395 10 1 4 5.2 CCCN(CC1CC1)c1cc(C(O)c2c(CC)cc(CC)cc2CC)nc(C)n1 10.1016/j.bmcl.2004.05.072
20780186 93872 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 395 5 0 5 5.1 CCN(CC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL247957 93872 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 395 5 0 5 5.1 CCN(CC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
20780149 67306 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 482 8 0 4 7.2 CCCN(CCC1CC1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL188358 67306 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 482 8 0 4 7.2 CCCN(CCC1CC1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
10737736 58745 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 367 2 0 3 5.4 Cc1cc(C)c2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL168590 58745 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 367 2 0 3 5.4 Cc1cc(C)c2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
21916261 7504 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 404 3 0 4 5.1 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN2CC=CCC2)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1087172 7504 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 404 3 0 4 5.1 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN2CC=CCC2)c(C)c1 10.1016/j.bmcl.2010.01.127
10545026 57890 1 None - 1 Rat 5.4 pKi = 5.4 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 339 2 0 3 3.5 Cc1cc(C)nc(N(C)c2ccccc2I)n1 10.1021/jm980222w
CHEMBL167217 57890 1 None - 1 Rat 5.4 pKi = 5.4 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 339 2 0 3 3.5 Cc1cc(C)nc(N(C)c2ccccc2I)n1 10.1021/jm980222w
53309547 63997 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 393 9 1 3 7.0 CCCCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1807037 63997 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 393 9 1 3 7.0 CCCCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(CC)CC 10.1021/jm200365y
15490819 98149 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 438 6 1 4 6.5 CCN(c1nc(C)cc(-c2ccccc2NC)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL273745 98149 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 438 6 1 4 6.5 CCN(c1nc(C)cc(-c2ccccc2NC)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
44341718 97384 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 446 9 0 4 7.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C(C)C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL269690 97384 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 446 9 0 4 7.7 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C(C)C)nc12 10.1016/s0960-894x(03)00621-8
10165732 64310 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 537 9 1 5 8.3 CCCN(Cc1ccc(OC)cc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181084 64310 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 537 9 1 5 8.3 CCCN(Cc1ccc(OC)cc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
20780140 124064 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 494 7 0 4 7.2 CCCN(Cc1c(C(F)(F)F)nc2n(-c3ccc(Cl)cc3Cl)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL363218 124064 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 494 7 0 4 7.2 CCCN(Cc1c(C(F)(F)F)nc2n(-c3ccc(Cl)cc3Cl)c3ccccc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
44460572 104762 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 398 7 1 3 6.1 Cc1ccccc1C(Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
CHEMBL310773 104762 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 398 7 1 3 6.1 Cc1ccccc1C(Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
22324329 104137 0 None - 1 Human 7.4 pKi = 7.4 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 373 9 0 6 3.9 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL309440 104137 0 None - 1 Human 7.4 pKi = 7.4 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 373 9 0 6 3.9 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
11122528 65228 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 413 10 0 7 4.0 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(OC)cc(OC)cc2OC)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL182643 65228 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 413 10 0 7 4.0 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(OC)cc(OC)cc2OC)c1C 10.1016/j.bmcl.2004.05.072
44392773 66657 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 349 7 0 4 4.4 C=CCN(CC=C)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL185329 66657 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 349 7 0 4 4.4 C=CCN(CC=C)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
10786842 57520 1 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 395 4 0 3 5.0 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1I 10.1021/jm980223o
CHEMBL166162 57520 1 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 395 4 0 3 5.0 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1I 10.1021/jm980223o
10786842 57520 1 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 395 4 0 3 5.0 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1I 10.1021/jm980222w
CHEMBL166162 57520 1 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 395 4 0 3 5.0 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1I 10.1021/jm980222w
44308172 162687 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 377 6 1 5 5.2 CCCCCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL417039 162687 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 377 6 1 5 5.2 CCCCCNc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
21916214 7580 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 524 7 0 4 7.0 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN(CCc2ccccc2)CC(F)(F)F)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1087803 7580 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 524 7 0 4 7.0 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN(CCc2ccccc2)CC(F)(F)F)c(C)c1 10.1016/j.bmcl.2010.01.127
10301060 64865 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 507 8 1 4 8.3 CCCN(Cc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL182133 64865 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 507 8 1 4 8.3 CCCN(Cc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
10527943 59047 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 459 8 1 7 4.5 CCCC(CN(C)C)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169421 59047 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 459 8 1 7 4.5 CCCC(CN(C)C)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44392747 66321 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 367 5 0 5 3.9 COC[C@@H]1CCCN1c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL184963 66321 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 367 5 0 5 3.9 COC[C@@H]1CCCN1c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
44341857 110420 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 459 7 0 5 6.0 CCCCN(CC1CCCN1C)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL324497 110420 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 459 7 0 5 6.0 CCCCN(CC1CCCN1C)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
44443593 94333 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 406 10 1 6 5.3 CCOCC(Nc1nc(CC)c(Oc2cc(C)ccn2)nc1CC)c1ccccc1 10.1016/j.bmcl.2007.09.008
CHEMBL250618 94333 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 406 10 1 6 5.3 CCOCC(Nc1nc(CC)c(Oc2cc(C)ccn2)nc1CC)c1ccccc1 10.1016/j.bmcl.2007.09.008
11727011 203703 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 321 4 2 3 4.2 CC(=O)/C(=N\c1ccc(Cl)cc1)NNc1ccccc1Cl 10.1021/jm025512y
CHEMBL67570 203703 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 321 4 2 3 4.2 CC(=O)/C(=N\c1ccc(Cl)cc1)NNc1ccccc1Cl 10.1021/jm025512y
44317976 104764 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 415 6 2 4 6.1 COc1ccc(C(=O)C(Nc2ccc(Cl)cc2Cl)c2ccccc2C)cc1O 10.1021/jm049974i
CHEMBL310783 104764 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 415 6 2 4 6.1 COc1ccc(C(=O)C(Nc2ccc(Cl)cc2Cl)c2ccccc2C)cc1O 10.1021/jm049974i
44318168 206015 0 None - 1 Human 7.4 pKi = 7.4 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 389 9 0 5 4.4 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(CCF)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL84974 206015 0 None - 1 Human 7.4 pKi = 7.4 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 389 9 0 5 4.4 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(CCF)c1=O 10.1016/s0960-894x(03)00483-9
11235365 66285 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 414 7 0 6 5.1 CCCN(CCC)c1c(Cl)c(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL184740 66285 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 414 7 0 6 5.1 CCCN(CCC)c1c(Cl)c(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
10672294 59104 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 477 10 0 8 4.2 CCOCC(COCC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169751 59104 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 477 10 0 8 4.2 CCOCC(COCC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10166079 123113 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 547 7 1 4 8.4 FC(F)(F)CN(Cc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL361108 123113 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 547 7 1 4 8.4 FC(F)(F)CN(Cc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
10833915 120745 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 384 9 0 8 2.7 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1 10.1021/jm980224g
CHEMBL355008 120745 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 384 9 0 8 2.7 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1 10.1021/jm980224g
11282674 73917 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 463 9 1 6 6.0 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCCCCC#N)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL201982 73917 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 463 9 1 6 6.0 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCCCCC#N)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
11677548 135178 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 374 3 0 4 5.2 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3CCN2CC(C)C 10.1021/jm049085v
CHEMBL371981 135178 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 374 3 0 4 5.2 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3CCN2CC(C)C 10.1021/jm049085v
44443580 94111 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 353 6 2 5 5.1 CCC(CC)Nc1nc(C)c(Nc2ncc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2007.09.008
CHEMBL249191 94111 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 353 6 2 5 5.1 CCC(CC)Nc1nc(C)c(Nc2ncc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2007.09.008
44318106 106133 0 None - 1 Human 8.4 pKi = 8.4 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 385 9 0 5 4.7 CCCN(CCC)c1c(CC)nc(-c2c(C)cc(C)cc2OC)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL313479 106133 0 None - 1 Human 8.4 pKi = 8.4 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 385 9 0 5 4.7 CCCN(CCC)c1c(CC)nc(-c2c(C)cc(C)cc2OC)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
10790606 58098 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 471 9 0 6 5.2 C=CCN(CC=C)c1nc(C)nc(N(CC)c2ccc(OC(F)(F)F)cc2Br)n1 10.1021/jm980222w
CHEMBL167463 58098 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 471 9 0 6 5.2 C=CCN(CC=C)c1nc(C)nc(N(CC)c2ccc(OC(F)(F)F)cc2Br)n1 10.1021/jm980222w
10741479 58826 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 433 9 0 5 5.9 CCCN(CCC)c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL168844 58826 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 433 9 0 5 5.9 CCCN(CCC)c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10502738 165705 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 429 9 0 5 5.4 C=CCN(CC=C)c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL424555 165705 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 429 9 0 5 5.4 C=CCN(CC=C)c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10808915 120813 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 366 7 1 6 4.8 CCCC(CCC)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL355689 120813 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 366 7 1 6 4.8 CCCC(CCC)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
44341815 9458 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 448 10 0 5 6.3 CCCCCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL111838 9458 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 448 10 0 5 6.3 CCCCCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
11417694 67453 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 382 7 1 5 4.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1016/j.bmcl.2015.10.010
CHEMBL189089 67453 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 382 7 1 5 4.4 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(OC)cc1C 10.1016/j.bmcl.2015.10.010
44307724 102179 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 371 6 0 5 4.9 CCCN(CCC)c1nc(C)nc2c(-c3ccc(Cl)cc3C)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL302742 102179 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 371 6 0 5 4.9 CCCN(CCC)c1nc(C)nc2c(-c3ccc(Cl)cc3C)n(C)nc12 10.1016/s0960-894x(02)00358-x
11178741 106382 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 426 10 0 5 6.3 CCCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL3085414 106382 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 426 10 0 5 6.3 CCCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL3139324 106382 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 426 10 0 5 6.3 CCCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
9868427 63840 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 450 5 0 6 6.3 CCN(CC)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
CHEMBL18029 63840 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 450 5 0 6 6.3 CCN(CC)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
9956594 98124 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 474 7 0 6 5.7 CCCN(CC1CC1)c1nc(C)nc2c1sc(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
CHEMBL273559 98124 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 474 7 0 6 5.7 CCCN(CC1CC1)c1nc(C)nc2c1sc(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
44341491 9490 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 376 5 0 4 5.5 CCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112031 9490 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 376 5 0 4 5.5 CCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9868427 63840 0 None - 1 Human 8.4 pKi = 8.4 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptorsCompound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors
ChEMBL 450 5 0 6 6.3 CCN(CC)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1021/jm990590f
CHEMBL18029 63840 0 None - 1 Human 8.4 pKi = 8.4 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptorsCompound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors
ChEMBL 450 5 0 6 6.3 CCN(CC)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1021/jm990590f
22249094 63940 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 365 7 1 3 6.2 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806728 63940 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 365 7 1 3 6.2 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(CC)CC 10.1021/jm200365y
10223332 63948 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 411 9 1 5 5.8 CCc1nc(-c2ccc(OC)cc2OC(F)(F)F)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806736 63948 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 411 9 1 5 5.8 CCc1nc(-c2ccc(OC)cc2OC(F)(F)F)c(CC)nc1NC(CC)CC 10.1021/jm200365y
9801390 109735 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 404 7 0 4 6.4 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(CC)c12 10.1016/s0960-894x(03)00621-8
CHEMBL322969 109735 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 404 7 0 4 6.4 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(CC)c12 10.1016/s0960-894x(03)00621-8
46871760 6810 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 472 7 0 4 6.7 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3Cl)c(Cl)cn12)CC1CC1 10.1016/j.bmcl.2010.04.094
CHEMBL1083921 6810 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 472 7 0 4 6.7 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3Cl)c(Cl)cn12)CC1CC1 10.1016/j.bmcl.2010.04.094
122193717 123956 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 472 6 1 4 6.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628734 123956 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 472 6 1 4 6.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C(C)(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
53310133 63944 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 385 10 1 5 5.7 CCc1nc(-c2ccc(OC(C)C)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806732 63944 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 385 10 1 5 5.7 CCc1nc(-c2ccc(OC(C)C)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
9951076 67411 2 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1021/jm040058e
CHEMBL188844 67411 2 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1021/jm040058e
CHEMBL2165204 67411 2 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 7 0 6 4.1 CCCN(CCC)c1cc(C)nc2c(-c3ccc(N(C)C)nc3)c(C)nn12 10.1021/jm040058e
11177298 122982 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 408 9 0 6 5.2 CCCCN(CCCC)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL360851 122982 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 408 9 0 6 5.2 CCCCN(CCCC)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
11224781 124523 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 415 6 0 3 7.0 CCCC(CCC)N1CCc2cn(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL364016 124523 0 None - 1 Human 8.4 pKi = 8.4 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 415 6 0 3 7.0 CCCC(CCC)N1CCc2cn(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
10717500 120251 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 7 0 5 5.6 CCCCN(CC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL352340 120251 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 7 0 5 5.6 CCCCN(CC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10551312 120419 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 444 8 0 7 4.0 C=CCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL353732 120419 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 444 8 0 7 4.0 C=CCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
22249116 64001 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 353 6 1 4 5.4 CCC(CC)Nc1nc(C)c(-c2ccc(Cl)cc2Cl)nc1OC 10.1021/jm200365y
CHEMBL1807041 64001 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 353 6 1 4 5.4 CCC(CC)Nc1nc(C)c(-c2ccc(Cl)cc2Cl)nc1OC 10.1021/jm200365y
44384802 59935 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 381 6 0 6 4.0 CCCCN(CC)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00108-0
CHEMBL173196 59935 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 381 6 0 6 4.0 CCCCN(CC)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00108-0
9931098 58767 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 404 8 0 8 3.8 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL168676 58767 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 404 8 0 8 3.8 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
10717499 129399 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 7 1 5 6.0 CCCC(CC)Nc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL367110 129399 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 7 1 5 6.0 CCCC(CC)Nc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
9908466 114804 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 390 6 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL334039 114804 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 390 6 0 4 5.9 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
44341739 113501 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 392 6 1 5 4.5 CCCN(CCO)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL332040 113501 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 392 6 1 5 4.5 CCCN(CCO)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
44341737 114095 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 388 5 0 4 5.5 CCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL332721 114095 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 388 5 0 4 5.5 CCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
46872038 123957 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 430 6 1 4 5.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Br)cc1C 10.1016/j.bmcl.2015.10.010
CHEMBL3628735 123957 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 430 6 1 4 5.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Br)cc1C 10.1016/j.bmcl.2015.10.010
46872037 123958 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 430 6 1 4 5.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628736 123958 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 430 6 1 4 5.2 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C)cc1Br 10.1016/j.bmcl.2015.10.010
122193718 123959 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 386 6 1 4 5.1 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C)cc1Cl 10.1016/j.bmcl.2015.10.010
CHEMBL3628737 123959 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 386 6 1 4 5.1 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(C)cc1Cl 10.1016/j.bmcl.2015.10.010
10200724 63975 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 395 8 1 4 5.9 CCc1nc(-c2ccc(OC)cc2C(F)(F)F)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806956 63975 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 395 8 1 4 5.9 CCc1nc(-c2ccc(OC)cc2C(F)(F)F)c(CC)nc1NC(CC)CC 10.1021/jm200365y
22248884 64006 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 397 8 1 5 5.3 CCc1nc(NC(CC)CC)c(OC)nc1-c1ccc(C(F)(F)F)cc1OC 10.1021/jm200365y
CHEMBL1807050 64006 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 397 8 1 5 5.3 CCc1nc(NC(CC)CC)c(OC)nc1-c1ccc(C(F)(F)F)cc1OC 10.1021/jm200365y
CHEMBL2372650 210279 0 None 2 2 Human 8.4 pKi = 8.4 Binding
Binding affinity of the receptor corticotropin releasing factor receptor with peptidic agonistsBinding affinity of the receptor corticotropin releasing factor receptor with peptidic agonists
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCCN1C(=O)[C@@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](N)CO)[C@@H](C)CC)[C@@H](C)O)C(C)C)[C@@H](C)CC)C(N)=O 10.1021/jm990590f
10375 2739 18 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm050384+
9888194 2739 18 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm050384+
CHEMBL188907 2739 18 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm050384+
10552437 59110 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 472 10 1 6 6.6 CCCCC(CCCC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169781 59110 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 472 10 1 6 6.6 CCCCC(CCCC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341875 168085 1 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 400 6 0 2 7.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)ccc12 10.1016/s0960-894x(03)00684-x
CHEMBL432607 168085 1 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 400 6 0 2 7.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)ccc12 10.1016/s0960-894x(03)00684-x
21916240 7071 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 7 0 4 6.1 C=CCN(CCC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1084999 7071 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 7 0 4 6.1 C=CCN(CCC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
9912040 120769 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 458 8 0 7 4.3 COCCN(CC1CC1)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL355329 120769 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 458 8 0 7 4.3 COCCN(CC1CC1)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
15490820 168726 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 5 0 4 6.6 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(C(C)=O)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL436978 168726 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 5 0 4 6.6 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(C(C)=O)cc1Br 10.1016/s0960-894x(99)00132-8
23595014 64011 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 385 8 1 5 5.3 CCC(CC)Nc1nc(C)c(-c2ccc(OC(F)F)cc2Cl)nc1OC 10.1021/jm200365y
CHEMBL1807055 64011 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 385 8 1 5 5.3 CCC(CC)Nc1nc(C)c(-c2ccc(OC(F)F)cc2Cl)nc1OC 10.1021/jm200365y
10695347 59070 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 461 9 0 7 4.1 COCCN(CCOC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169561 59070 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 461 9 0 7 4.1 COCCN(CCOC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10741252 120254 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 10 0 8 4.1 COCCN(CCOC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1SC 10.1021/jm980224g
CHEMBL352353 120254 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 10 0 8 4.1 COCCN(CCOC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1SC 10.1021/jm980224g
44341901 10071 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 414 9 0 5 6.0 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(OC)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL115349 10071 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 414 9 0 5 6.0 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(OC)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
10303689 123828 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 579 8 1 4 9.0 Fc1ccc(CN(CCC(F)(F)F)Cc2sc(Nc3c(Cl)cc(Cl)cc3Cl)nc2C(F)(F)F)cc1 10.1016/j.bmcl.2004.10.055
CHEMBL362448 123828 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 579 8 1 4 9.0 Fc1ccc(CN(CCC(F)(F)F)Cc2sc(Nc3c(Cl)cc(Cl)cc3Cl)nc2C(F)(F)F)cc1 10.1016/j.bmcl.2004.10.055
11429341 67362 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 394 8 1 6 5.2 CCCC(CCC)Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL188609 67362 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 394 8 1 6 5.2 CCCC(CCC)Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
44392678 64646 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 366 7 1 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(NC)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL181812 64646 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 366 7 1 6 4.4 CCCN(CCC)c1cc(C)nc2c(-c3ncc(NC)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
44392749 66708 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 352 6 1 6 3.9 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3N)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL185570 66708 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 352 6 1 6 3.9 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3N)c(C)nn12 10.1016/j.bmcl.2004.05.056
11153953 10144 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 404 8 1 3 6.6 CCCCN(CCCC)c1cc(C)[nH]c2c(-c3ccc(Cl)cc3Cl)nnc1-2 10.1016/s0960-894x(03)00621-8
CHEMBL115759 10144 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 404 8 1 3 6.6 CCCCN(CCCC)c1cc(C)[nH]c2c(-c3ccc(Cl)cc3Cl)nnc1-2 10.1016/s0960-894x(03)00621-8
44305256 102357 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 376 6 0 4 5.6 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cnn12 10.1016/s0960-894x(98)00372-2
CHEMBL303789 102357 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 376 6 0 4 5.6 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cnn12 10.1016/s0960-894x(98)00372-2
11749772 68647 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 394 5 0 5 4.6 CCC(COC)N1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL191903 68647 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 394 5 0 5 4.6 CCC(COC)N1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
44318123 205693 0 None - 1 Human 5.4 pKi = 5.4 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 403 11 0 7 3.5 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(CCOC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL82275 205693 0 None - 1 Human 5.4 pKi = 5.4 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 403 11 0 7 3.5 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(CCOC)c1=O 10.1016/s0960-894x(03)00483-9
22248970 63989 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 368 6 0 3 6.5 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1SC(C)CC 10.1021/jm200365y
CHEMBL1807029 63989 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 368 6 0 3 6.5 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1SC(C)CC 10.1021/jm200365y
44443567 154987 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 300 6 1 5 4.2 CCC(CC)Nc1nc(C)c(Oc2cc(C)ccn2)nc1C 10.1016/j.bmcl.2007.09.008
CHEMBL401295 154987 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 300 6 1 5 4.2 CCC(CC)Nc1nc(C)c(Oc2cc(C)ccn2)nc1C 10.1016/j.bmcl.2007.09.008
20780131 67545 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 504 7 0 4 7.6 CCCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL189714 67545 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 504 7 0 4 7.6 CCCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
10645784 57481 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 419 8 1 5 5.8 CCC(CC)Nc1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL165824 57481 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 419 8 1 5 5.8 CCC(CC)Nc1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10553475 169495 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 500 10 0 8 5.2 CCCCN(Cc1nnnn1C)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL443235 169495 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 500 10 0 8 5.2 CCCCN(Cc1nnnn1C)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
20780279 122321 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 434 6 0 4 4.9 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL359832 122321 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 434 6 0 4 4.9 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780026 122347 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 454 6 0 4 5.3 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1c(C)cc(C)cc1Cl 10.1016/j.bmcl.2005.05.117
CHEMBL359936 122347 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 454 6 0 4 5.3 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)F)CCN2c1c(C)cc(C)cc1Cl 10.1016/j.bmcl.2005.05.117
44305246 102323 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 374 2 0 4 5.3 Cc1cc(N2CCCCC2)n2nc(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(98)00372-2
CHEMBL303593 102323 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 374 2 0 4 5.3 Cc1cc(N2CCCCC2)n2nc(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(98)00372-2
20780161 93722 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 401 7 0 5 5.3 C=CCN(CCC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL247152 93722 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 401 7 0 5 5.3 C=CCN(CCC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
44446741 94650 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 489 10 1 5 6.3 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCC(O)CC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL252494 94650 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 489 10 1 5 6.3 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCC(O)CC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
20780154 67554 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 596 9 0 4 8.6 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3ccc(C(C)C)cc3Br)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL189798 67554 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 596 9 0 4 8.6 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3ccc(C(C)C)cc3Br)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
20780272 63839 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 430 7 0 4 5.6 CCCN(Cc1ccccc1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL180284 63839 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 430 7 0 4 5.6 CCCN(Cc1ccccc1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780061 93329 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 455 9 0 7 4.3 COCCN(CCOC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL245298 93329 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 455 9 0 7 4.3 COCCN(CCOC)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
11257259 68324 0 None - 1 Human 5.4 pKi = 5.4 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 371 10 0 4 5.5 CCCC(CCC)N1CCc2cn(CCCOC(C)C)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL191650 68324 0 None - 1 Human 5.4 pKi = 5.4 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 371 10 0 4 5.5 CCCC(CCC)N1CCc2cn(CCCOC(C)C)c3nc(C)cc1c23 10.1021/jm050070m
10946918 203678 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 312 4 2 4 3.6 CC(=O)/C(=N\Nc1ccccc1C#N)Nc1cccc(Cl)c1 10.1021/jm025512y
CHEMBL67448 203678 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 312 4 2 4 3.6 CC(=O)/C(=N\Nc1ccccc1C#N)Nc1cccc(Cl)c1 10.1021/jm025512y
10500311 59771 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 385 8 0 9 1.9 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)nc1C 10.1021/jm980224g
CHEMBL172570 59771 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 385 8 0 9 1.9 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)nc1C 10.1021/jm980224g
11045497 102391 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 321 4 2 3 4.4 CC(=O)/C(=N\Nc1ccccc1Cl)Nc1cccc(Cl)c1 10.1021/jm025512y
CHEMBL303931 102391 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 321 4 2 3 4.4 CC(=O)/C(=N\Nc1ccccc1Cl)Nc1cccc(Cl)c1 10.1021/jm025512y
11502109 122349 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 394 7 0 4 4.8 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL359956 122349 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 394 7 0 4 4.8 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
44446723 94806 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 378 8 0 4 5.9 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253492 94806 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 378 8 0 4 5.9 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
44389111 172437 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 525 8 1 4 8.4 CCCN(Cc1ccccc1F)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL447836 172437 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 525 8 1 4 8.4 CCCN(Cc1ccccc1F)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
44385503 61334 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 461 7 1 7 4.2 CCC(COC)Nc1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL176721 61334 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 461 7 1 7 4.2 CCC(COC)Nc1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
44341949 110790 1 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 318 6 0 2 5.8 CCCN(CCC)c1cc(C)nc2c(-c3ccccc3)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL326074 110790 1 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 318 6 0 2 5.8 CCCN(CCC)c1cc(C)nc2c(-c3ccccc3)cccc12 10.1016/s0960-894x(03)00684-x
10206448 64570 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 485 9 1 4 7.9 CCCN(CCC1CC1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181566 64570 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 485 9 1 4 7.9 CCCN(CCC1CC1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
20780033 64835 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 448 7 0 4 5.7 CCCN(Cc1cccc(F)c1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL181989 64835 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 448 7 0 4 5.7 CCCN(Cc1cccc(F)c1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780075 67240 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 558 7 0 4 8.2 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC(F)(F)F)Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL187975 67240 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 558 7 0 4 8.2 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC(F)(F)F)Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
11155555 78343 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 466 8 0 5 6.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)[C@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
CHEMBL2093959 78343 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 466 8 0 5 6.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)[C@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
CHEMBL2110007 78343 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 466 8 0 5 6.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)[C@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
10402860 103125 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 305 4 2 3 3.7 CC(=O)/C(=N\c1cccc(F)c1)NNc1ccccc1Cl 10.1021/jm025512y
CHEMBL307795 103125 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 305 4 2 3 3.7 CC(=O)/C(=N\c1cccc(F)c1)NNc1ccccc1Cl 10.1021/jm025512y
11778680 203706 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 285 4 2 3 3.4 CC(=O)/C(=N\c1cccc(F)c1)NNc1ccccc1C 10.1021/jm025512y
CHEMBL67603 203706 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 285 4 2 3 3.4 CC(=O)/C(=N\c1cccc(F)c1)NNc1ccccc1C 10.1021/jm025512y
44347421 16430 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 414 10 0 8 3.1 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL123197 16430 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 414 10 0 8 3.1 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(OC)cc3OC)c(C)nn12 10.1016/j.bmcl.2004.05.019
9828535 165561 0 None -1 2 Rat 7.4 pKi = 7.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980223o
CHEMBL424204 165561 0 None -1 2 Rat 7.4 pKi = 7.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980223o
CHEMBL43216 165561 0 None -1 2 Rat 7.4 pKi = 7.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 437 6 0 8 3.0 CCN(c1nc(C)nc(N2CCOCC2)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980223o
21916338 6571 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 542 7 0 4 7.7 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1083035 6571 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 542 7 0 4 7.7 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
20780150 145100 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 429 8 0 5 5.9 CCCN(CCC1CC1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL391170 145100 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 429 8 0 5 5.9 CCCN(CCC1CC1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
10164617 64472 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 511 7 1 4 7.6 FC(F)(F)CN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
CHEMBL181381 64472 0 None - 1 Human 7.4 pKi = 7.4 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 511 7 1 4 7.6 FC(F)(F)CN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
46890888 6526 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 475 6 0 5 5.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)CCc4ccccn4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082807 6526 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 475 6 0 5 5.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)CCc4ccccn4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
10477079 94441 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 417 8 1 5 5.8 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cccc(C)c2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL251199 94441 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 417 8 1 5 5.8 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cccc(C)c2)nc1CC 10.1016/j.bmcl.2007.09.008
44317800 205214 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 362 7 1 3 5.2 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2C)c(F)c1 10.1021/jm049974i
CHEMBL78608 205214 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 362 7 1 3 5.2 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2C)c(F)c1 10.1021/jm049974i
9865434 68029 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 394 7 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccccc3OC)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL191395 68029 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 394 7 0 6 4.3 CCCC(CCC)N1CCn2c(=O)n(-c3ccccc3OC)c3nc(C)cc1c32 10.1021/jm050384+
10526779 58129 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 432 9 1 4 6.7 CCC(CC)CNc1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL167738 58129 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 432 9 1 4 6.7 CCC(CC)CNc1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10763375 115344 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 397 3 0 5 5.5 Cc1nc(N(C)c2ccccc2)n2nc(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1021/jm9904351
CHEMBL334935 115344 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 397 3 0 5 5.5 Cc1nc(N(C)c2ccccc2)n2nc(C)c(-c3ccc(Cl)cc3Cl)c2n1 10.1021/jm9904351
CHEMBL2372938 210319 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)C(CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm034180+
21916309 7273 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 530 7 0 4 7.1 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC(F)(F)C(F)(F)F 10.1016/j.bmcl.2010.04.094
CHEMBL1085989 7273 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 530 7 0 4 7.1 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC(F)(F)C(F)(F)F 10.1016/j.bmcl.2010.04.094
11486120 62994 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 390 10 0 5 5.3 CCCCC(CC)N(CC1CC1)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL178618 62994 0 None - 1 Human 6.4 pKi = 6.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 390 10 0 5 5.3 CCCCC(CC)N(CC1CC1)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
21916155 7506 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 424 3 0 5 4.9 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN2CCSCC2)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1087174 7506 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 424 3 0 5 4.9 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN2CCSCC2)c(C)c1 10.1016/j.bmcl.2010.01.127
10739049 57771 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 387 2 0 3 5.7 Cc1cc(Cl)nc2c1c(C#N)cn2-c1ccc(C(C)C)cc1Br 10.1021/jm980223o
CHEMBL166946 57771 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 387 2 0 3 5.7 Cc1cc(Cl)nc2c1c(C#N)cn2-c1ccc(C(C)C)cc1Br 10.1021/jm980223o
54586411 61652 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity to CRHRBinding affinity to CRHR
ChEMBL 387 5 1 5 4.6 CCN(CCN)c1nc(C)nc2c1c1ccccc1n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.12.116
CHEMBL1771267 61652 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity to CRHRBinding affinity to CRHR
ChEMBL 387 5 1 5 4.6 CCN(CCN)c1nc(C)nc2c1c1ccccc1n2-c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.12.116
CHEMBL2372900 210305 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm034180+
9870876 64611 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 506 7 0 6 7.8 CCC(C)N(c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br)C(C)CC 10.1016/s0960-894x(99)00159-6
CHEMBL18173 64611 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 506 7 0 6 7.8 CCC(C)N(c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br)C(C)CC 10.1016/s0960-894x(99)00159-6
10316753 60491 0 None - 1 Human 5.4 pKi = 5.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 364 7 1 3 5.2 CCCN(c1n[nH]c(-c2ccc(Cl)cc2Cl)n1)C(C1CC1)C1CC1 10.1021/jm049339c
CHEMBL175536 60491 0 None - 1 Human 5.4 pKi = 5.4 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 364 7 1 3 5.2 CCCN(c1n[nH]c(-c2ccc(Cl)cc2Cl)n1)C(C1CC1)C1CC1 10.1021/jm049339c
10025032 155238 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2ccc(C)cn2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL402717 155238 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2ccc(C)cn2)nc1CC 10.1016/j.bmcl.2007.09.008
20780068 124086 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 536 8 0 4 7.8 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC4CC4)CCC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL363281 124086 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 536 8 0 4 7.8 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC4CC4)CCC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
10549751 120435 1 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 414 3 0 6 4.4 Cc1nc(N2CCCCC2)c2nnn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980224g
CHEMBL353856 120435 1 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 414 3 0 6 4.4 Cc1nc(N2CCCCC2)c2nnn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980224g
44341777 10208 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 416 7 0 4 6.4 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL115999 10208 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 416 7 0 4 6.4 CCCN(CC1CC1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
10831554 58035 1 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 347 4 0 3 5.1 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980223o
CHEMBL167264 58035 1 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 347 4 0 3 5.1 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980223o
10831554 58035 1 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 347 4 0 3 5.1 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
CHEMBL167264 58035 1 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 347 4 0 3 5.1 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)C)cc1Br 10.1021/jm980222w
10155816 63988 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 366 7 0 3 6.1 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1OC(CC)CC 10.1021/jm200365y
CHEMBL1807028 63988 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 366 7 0 3 6.1 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1OC(CC)CC 10.1021/jm200365y
18672272 62493 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 525 8 1 4 8.0 FC(F)(F)CCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
CHEMBL178081 62493 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 525 8 1 4 8.0 FC(F)(F)CCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
11247792 78344 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCC[C@H](c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL2093960 78344 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCC[C@H](c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL2110008 78344 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCC[C@H](c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
11383383 123941 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 378 10 0 5 5.3 CCCCC(CC)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL362847 123941 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 378 10 0 5 5.3 CCCCC(CC)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
11154954 67976 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 442 7 0 7 3.7 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(S(C)(=O)=O)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL191188 67976 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 442 7 0 7 3.7 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(S(C)(=O)=O)cc3)c3nc(C)cc1c32 10.1021/jm050384+
23000016 9566 1 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 301 1 0 1 5.8 Cc1cc(C)c2cccc(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(03)00684-x
CHEMBL112389 9566 1 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 301 1 0 1 5.8 Cc1cc(C)c2cccc(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(03)00684-x
44306185 102803 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 367 9 0 5 4.6 CCCN(c1nccc(-c2ccc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL305354 102803 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 367 9 0 5 4.6 CCCN(c1nccc(-c2ccc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
44352436 116994 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 437 8 1 4 6.8 CCCN(Cc1sc(Nc2ccc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL338780 116994 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 437 8 1 4 6.8 CCCN(Cc1sc(Nc2ccc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
44387214 60806 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 458 7 0 5 5.5 CCCCN(CC)c1nc(C)cc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL176176 60806 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 458 7 0 5 5.5 CCCCN(CC)c1nc(C)cc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
44443605 94074 0 None - 1 Human 5.3 pKi = 5.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 378 8 2 6 4.2 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(CO)c1ccccc1 10.1016/j.bmcl.2007.09.008
CHEMBL249012 94074 0 None - 1 Human 5.3 pKi = 5.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 378 8 2 6 4.2 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(CO)c1ccccc1 10.1016/j.bmcl.2007.09.008
44317728 105608 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 432 7 1 3 6.4 Cc1ccccc1C(Nc1ccc(Cl)cc1C(F)(F)F)C(=O)CCc1ccncc1 10.1021/jm049974i
CHEMBL312239 105608 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 432 7 1 3 6.4 Cc1ccccc1C(Nc1ccc(Cl)cc1C(F)(F)F)C(=O)CCc1ccncc1 10.1021/jm049974i
44318109 206004 0 None - 1 Human 7.3 pKi = 7.3 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 385 8 0 5 5.1 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(C(C)C)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL84892 206004 0 None - 1 Human 7.3 pKi = 7.3 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 385 8 0 5 5.1 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(C(C)C)c1=O 10.1016/s0960-894x(03)00483-9
10497535 59112 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 342 2 0 2 5.5 Cc1cc(C)c2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL169784 59112 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 342 2 0 2 5.5 Cc1cc(C)c2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
44384780 59777 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 461 7 0 7 3.8 CCN(CCOC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL172606 59777 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 461 7 0 7 3.8 CCN(CCOC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
22324333 105620 0 None - 1 Human 6.3 pKi = 6.3 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 359 8 0 6 3.4 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(C)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL312336 105620 0 None - 1 Human 6.3 pKi = 6.3 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 359 8 0 6 3.4 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(C)c1=O 10.1016/s0960-894x(03)00483-9
44392776 65271 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 373 5 0 4 5.4 CCN(c1ccccc1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL182825 65271 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 373 5 0 4 5.4 CCN(c1ccccc1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
46891115 6809 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 418 7 0 4 5.7 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)ccn12)CC1CC1 10.1016/j.bmcl.2010.04.094
CHEMBL1083920 6809 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 418 7 0 4 5.7 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)ccn12)CC1CC1 10.1016/j.bmcl.2010.04.094
11032842 204092 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 267 4 2 3 3.2 CC(=O)/C(=N\c1cccc(C)c1)NNc1ccccc1 10.1021/jm025512y
CHEMBL70195 204092 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 267 4 2 3 3.2 CC(=O)/C(=N\c1cccc(C)c1)NNc1ccccc1 10.1021/jm025512y
44443642 167536 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cccc(C)n2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL430019 167536 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cccc(C)n2)nc1CC 10.1016/j.bmcl.2007.09.008
10623894 59130 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 461 10 0 9 2.8 COCCN(CCOC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1S(C)(=O)=O 10.1021/jm980224g
CHEMBL169841 59130 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 461 10 0 9 2.8 COCCN(CCOC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1S(C)(=O)=O 10.1021/jm980224g
11796523 120374 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 422 8 0 6 4.6 CCN(CC)c1cc(C)nc(N(CC)c2c(Br)cc(OC)cc2OC)n1 10.1021/jm980222w
CHEMBL353296 120374 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 422 8 0 6 4.6 CCN(CC)c1cc(C)nc(N(CC)c2c(Br)cc(OC)cc2OC)n1 10.1021/jm980222w
44380639 120807 1 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 381 3 0 3 4.6 Cc1cc(C)nc(N(C)c2ccc(C(C)C)cc2I)n1 10.1021/jm980223o
CHEMBL355624 120807 1 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 381 3 0 3 4.6 Cc1cc(C)nc(N(C)c2ccc(C(C)C)cc2I)n1 10.1021/jm980223o
20780051 93873 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 483 5 0 5 6.5 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCCC4Cc4ccccc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL247958 93873 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 483 5 0 5 6.5 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCCC4Cc4ccccc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
21916263 5588 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 420 7 0 4 5.8 C=CCN(CCC)Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
CHEMBL1077156 5588 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 420 7 0 4 5.8 C=CCN(CCC)Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
44381252 120482 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 493 10 0 10 2.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(Br)cc(OC)cc1N(C)C 10.1021/jm980224g
CHEMBL354280 120482 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 493 10 0 10 2.5 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1c(Br)cc(OC)cc1N(C)C 10.1021/jm980224g
44381175 58871 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 495 8 0 8 4.5 COCCN(Cc1cccnc1)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168858 58871 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 495 8 0 8 4.5 COCCN(Cc1cccnc1)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
127033837 138628 0 None -1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3901 126 54 50 -8.8 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)C1CCSSCCC(NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775831 138628 0 None -1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3901 126 54 50 -8.8 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)C1CCSSCCC(NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)NC(C)(C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL2372937 210318 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)C(CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm034180+
127034112 138609 0 None -1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4252 133 59 54 -8.7 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)C1CCSSCCC(NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)NC(Cc2ccc(NC(=O)[C@@H]3CC(=O)NC(=O)N3)cc2)C(=O)N[C@H](Cc2ccc(NC(N)=O)cc2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775707 138609 0 None -1 2 Human 7.3 pKi = 7.3 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 4252 133 59 54 -8.7 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)C1CCSSCCC(NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)NC(Cc2ccc(NC(=O)[C@@H]3CC(=O)NC(=O)N3)cc2)C(=O)N[C@H](Cc2ccc(NC(N)=O)cc2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
44392775 124647 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 399 10 0 6 4.6 CCCN(CC1CC1)c1cc(C(C)c2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL364117 124647 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 399 10 0 6 4.6 CCCN(CC1CC1)c1cc(C(C)c2c(OC)cc(OC)cc2OC)nc(C)n1 10.1016/j.bmcl.2004.05.072
46890768 6731 0 None - 1 Human 5.3 pKi = 5.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 488 6 0 4 7.1 CCN(Cc1ccccc1C)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1083720 6731 0 None - 1 Human 5.3 pKi = 5.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 488 6 0 4 7.1 CCN(Cc1ccccc1C)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
53310276 63983 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 380 7 1 4 4.9 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(C)CN(C)C 10.1021/jm200365y
CHEMBL1807023 63983 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 380 7 1 4 4.9 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1NC(C)CN(C)C 10.1021/jm200365y
19063905 202969 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 399 7 0 3 5.6 CCCN(c1ncc(C)c(-c2ccc(Br)cc2)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL63029 202969 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 399 7 0 3 5.6 CCCN(c1ncc(C)c(-c2ccc(Br)cc2)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
21916094 6572 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 560 7 0 4 7.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)Cc4cccc(F)c4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1083036 6572 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 560 7 0 4 7.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC(F)(F)F)Cc4cccc(F)c4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
11387007 168838 1 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 530 8 1 7 6.3 COC(=O)c1cccc(COc2ccc(S(=O)(=O)c3ccc(C)nc3Nc3c(C)cc(C)cc3C)cc2)c1 10.1016/j.bmcl.2005.10.097
CHEMBL437893 168838 1 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 530 8 1 7 6.3 COC(=O)c1cccc(COc2ccc(S(=O)(=O)c3ccc(C)nc3Nc3c(C)cc(C)cc3C)cc2)c1 10.1016/j.bmcl.2005.10.097
44446728 94836 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 362 7 0 3 6.2 CCCN(CCC)c1cnc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253701 94836 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 362 7 0 3 6.2 CCCN(CCC)c1cnc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
11175998 133618 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 364 4 0 4 5.0 CCCCN1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL371367 133618 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 364 4 0 4 5.0 CCCCN1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
10547488 103076 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 375 7 1 5 5.3 CCCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
CHEMBL307419 103076 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 375 7 1 5 5.3 CCCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
10808133 163421 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 355 9 1 5 5.3 CCCCN(CCCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
CHEMBL419636 163421 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 355 9 1 5 5.3 CCCCN(CCCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
10547488 103076 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 375 7 1 5 5.3 CCCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
CHEMBL307419 103076 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 375 7 1 5 5.3 CCCN(Cc1ccccc1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
10808133 163421 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 355 9 1 5 5.3 CCCCN(CCCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
CHEMBL419636 163421 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 355 9 1 5 5.3 CCCCN(CCCC)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
9931738 61169 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 416 8 0 8 3.2 COCCN(CCOC)c1nc(C)nc2c1sc(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
CHEMBL17656 61169 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 416 8 0 8 3.2 COCCN(CCOC)c1nc(C)nc2c1sc(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
10646276 57542 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 429 8 0 5 5.4 C=CCN(c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1)C1CC1 10.1021/jm980222w
CHEMBL166345 57542 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 429 8 0 5 5.4 C=CCN(c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1)C1CC1 10.1021/jm980222w
10694122 57548 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 433 9 0 5 5.9 CCCCN(CC)c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL166388 57548 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 433 9 0 5 5.9 CCCCN(CC)c1nc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10809708 57689 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 378 5 0 5 4.1 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(N(C)C)cc1OC 10.1021/jm980222w
CHEMBL166895 57689 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 378 5 0 5 4.1 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(N(C)C)cc1OC 10.1021/jm980222w
11795557 57840 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 404 7 0 5 4.8 CCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)=O)cc2Br)n1 10.1021/jm980222w
CHEMBL167177 57840 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 404 7 0 5 4.8 CCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)=O)cc2Br)n1 10.1021/jm980222w
10503074 58094 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 436 9 0 6 5.0 CCCN(CC1CC1)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
CHEMBL167428 58094 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 436 9 0 6 5.0 CCCN(CC1CC1)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
11796930 120440 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 430 8 0 4 6.2 CCCN(c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1)C1CC1 10.1021/jm980222w
CHEMBL353877 120440 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 430 8 0 4 6.2 CCCN(c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1)C1CC1 10.1021/jm980222w
10646531 120474 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 435 9 0 7 4.6 CCCN(CCC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
CHEMBL354178 120474 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 435 9 0 7 4.6 CCCN(CCC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
10838302 120491 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 475 9 0 6 5.6 CCCCN(CC)c1nc(C)nc(N(CC)c2ccc(OC(F)(F)F)cc2Br)n1 10.1021/jm980222w
CHEMBL354367 120491 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 475 9 0 6 5.6 CCCCN(CC)c1nc(C)nc(N(CC)c2ccc(OC(F)(F)F)cc2Br)n1 10.1021/jm980222w
10527467 120494 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 448 9 0 6 5.0 CCN(c1nc(C)nc(N(CC2CC2)CC2CC2)n1)c1ccc(N(C)C)cc1C(F)(F)F 10.1021/jm980222w
CHEMBL354395 120494 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 448 9 0 6 5.0 CCN(c1nc(C)nc(N(CC2CC2)CC2CC2)n1)c1ccc(N(C)C)cc1C(F)(F)F 10.1021/jm980222w
10366978 101385 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 459 7 0 6 4.9 CCCCN(CC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL297170 101385 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 459 7 0 6 4.9 CCCCN(CC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
9935525 58626 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 494 8 0 7 5.1 COCCN(Cc1ccccc1)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168449 58626 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 494 8 0 7 5.1 COCCN(Cc1ccccc1)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
11759092 10036 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 321 1 0 1 6.2 Cc1cc(Cl)c2cccc(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(03)00684-x
CHEMBL115119 10036 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 321 1 0 1 6.2 Cc1cc(Cl)c2cccc(-c3ccc(Cl)cc3Cl)c2n1 10.1016/s0960-894x(03)00684-x
9907170 178099 0 None 2 2 Rat 8.3 pKi = 8.3 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 365 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980223o
CHEMBL46479 178099 0 None 2 2 Rat 8.3 pKi = 8.3 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 365 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(OC)cc1OC 10.1021/jm980223o
10366978 101385 0 None - 1 Human 8.3 pKi = 8.3 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptorsCompound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors
ChEMBL 459 7 0 6 4.9 CCCCN(CC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1021/jm990590f
CHEMBL297170 101385 0 None - 1 Human 8.3 pKi = 8.3 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptorsCompound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors
ChEMBL 459 7 0 6 4.9 CCCCN(CC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1021/jm990590f
9800614 100467 5 None - 1 Human 8.3 pKi = 8.3 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm990590f
CHEMBL290762 100467 5 None - 1 Human 8.3 pKi = 8.3 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors.
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm990590f
3520 3267 54 None 1 2 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/s0960-894x(02)00358-x
9821250 3267 54 None 1 2 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/s0960-894x(02)00358-x
CHEMBL309138 3267 54 None 1 2 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1016/s0960-894x(02)00358-x
9800614 100467 5 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL290762 100467 5 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 390 6 0 4 5.9 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
137659453 159121 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]o-CRF from recombinant human CRF1 receptor expressed in CHO cellsDisplacement of [125I]o-CRF from recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 432 9 0 4 7.0 CCCCc1nn2c(N(CC)CCCC)cc(C)nc2c1-c1ccc(Cl)cc1Cl 10.1016/j.ejmech.2016.11.019
CHEMBL4097805 159121 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]o-CRF from recombinant human CRF1 receptor expressed in CHO cellsDisplacement of [125I]o-CRF from recombinant human CRF1 receptor expressed in CHO cells
ChEMBL 432 9 0 4 7.0 CCCCc1nn2c(N(CC)CCCC)cc(C)nc2c1-c1ccc(Cl)cc1Cl 10.1016/j.ejmech.2016.11.019
44446730 155560 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 388 7 0 3 6.5 CCCN(CC1CC1)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL404351 155560 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 388 7 0 3 6.5 CCCN(CC1CC1)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
10375 2739 18 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm049085v
9888194 2739 18 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm049085v
CHEMBL188907 2739 18 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 10.1021/jm049085v
9933199 71506 1 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 444 8 0 4 7.3 CCCCC(CCCC)N1CCn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c32 10.1021/jm049085v
CHEMBL196270 71506 1 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 444 8 0 4 7.3 CCCCC(CCCC)N1CCn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c32 10.1021/jm049085v
11718607 135222 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 414 4 0 4 6.0 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3C[C@H](C(C)C)N2CC1CC1 10.1021/jm049085v
CHEMBL372319 135222 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 414 4 0 4 6.0 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3C[C@H](C(C)C)N2CC1CC1 10.1021/jm049085v
9824168 67633 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 432 6 0 5 5.6 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL190488 67633 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 432 6 0 5 5.6 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c32 10.1021/jm050384+
10837003 59798 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 443 8 1 5 6.4 CCCCC(CC)Nc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL172684 59798 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 443 8 1 5 6.4 CCCCC(CC)Nc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341862 9538 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 392 8 0 4 6.3 CCCCN(CCCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112264 9538 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 392 8 0 4 6.3 CCCCN(CCCC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)nn(C)c12 10.1016/s0960-894x(03)00622-x
12086065 10835 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 406 7 0 5 5.1 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL117209 10835 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 406 7 0 5 5.1 CCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
10693263 59079 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 416 6 1 6 5.0 CCC(CC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169577 59079 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 416 6 1 6 5.0 CCC(CC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10549179 120816 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 403 8 0 7 4.4 CCCCN(CC)c1nc(C)nc2c1ncn2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
CHEMBL355721 120816 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 403 8 0 7 4.4 CCCCN(CC)c1nc(C)nc2c1ncn2-c1c(Cl)cc(OC)cc1OC 10.1021/jm980224g
20780267 6818 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 492 6 0 4 6.5 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CC4CC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1083933 6818 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 492 6 0 4 6.5 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CC4CC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
11386550 78330 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 466 8 0 5 6.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)[C@@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
CHEMBL2094043 78330 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 466 8 0 5 6.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)[C@@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
CHEMBL2109791 78330 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 466 8 0 5 6.5 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)[C@@H](CC)c1ccc(C(F)(F)F)cc1 10.1021/jm049339c
11383860 67023 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 394 7 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm040058e
CHEMBL187039 67023 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 394 7 0 6 4.7 CCCN(CCC)c1cc(C)nc2c(-c3c(C)cc(N(C)C)nc3C)c(C)nn12 10.1021/jm040058e
11201203 127279 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 7 0 6 5.2 CCCN(Cc1ccccc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL365841 127279 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 428 7 0 6 5.2 CCCN(Cc1ccccc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
20780254 6826 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 466 7 0 4 6.7 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC1CCC1 10.1016/j.bmcl.2010.04.094
CHEMBL1083952 6826 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 466 7 0 4 6.7 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC1CCC1 10.1016/j.bmcl.2010.04.094
122193719 123960 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 386 6 1 4 5.1 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1C 10.1016/j.bmcl.2015.10.010
CHEMBL3628738 123960 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 386 6 1 4 5.1 CCCCN(CC)c1cc(C)nc2c1NC(=O)CN2c1ccc(Cl)cc1C 10.1016/j.bmcl.2015.10.010
11362799 71272 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 408 8 0 6 5.1 CCCC(CCC)N1CCc2cn(-c3ccc(OC)nc3OC)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL195699 71272 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 408 8 0 6 5.1 CCCC(CCC)N1CCc2cn(-c3ccc(OC)nc3OC)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL386892 212399 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC1CCCCC1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N1)[C@@H](C)CC)C(N)=O 10.1021/jm034180+
10178818 63946 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 395 8 1 4 5.9 CCc1nc(-c2ccc(C(F)(F)F)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806734 63946 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 395 8 1 4 5.9 CCc1nc(-c2ccc(C(F)(F)F)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
11372928 170270 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 398 7 0 6 4.5 CCCN(CCC)c1c(F)c(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL444614 170270 0 None - 1 Human 8.3 pKi = 8.3 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 398 7 0 6 4.5 CCCN(CCC)c1c(F)c(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
10205521 168504 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 471 7 0 6 4.9 CCCN(CC1CC1)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL435345 168504 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 471 7 0 6 4.9 CCCN(CC1CC1)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
10593122 58763 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 338 5 1 6 4.0 CCC(CC)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL168664 58763 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 338 5 1 6 4.0 CCC(CC)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
44341636 9695 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 386 6 0 2 7.1 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL113097 9695 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 386 6 0 2 7.1 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
44341743 110583 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 418 8 0 4 5.6 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL325430 110583 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 418 8 0 4 5.6 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)cccc12 10.1016/s0960-894x(03)00684-x
11165678 78346 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 406 10 0 5 5.9 CCCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL2093962 78346 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 406 10 0 5 5.9 CCCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL2110010 78346 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 406 10 0 5 5.9 CCCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
18691320 4739 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 513 4 0 3 7.2 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(Br)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10373 4739 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 513 4 0 3 7.2 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1ccc(Br)cc1Br 10.1016/s0960-894x(99)00132-8
18691324 97006 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 434 5 0 4 6.4 CCN(c1nc(C)cc(-c2ccccc2C#N)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL266617 97006 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 434 5 0 4 6.4 CCN(c1nc(C)cc(-c2ccccc2C#N)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
10813902 58133 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 461 9 0 7 4.1 COCCN(CCOC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL167777 58133 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 461 9 0 7 4.1 COCCN(CCOC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
22249149 63995 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 367 7 1 4 5.6 CCc1nc(NC(CC)CC)c(OC)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
CHEMBL1807035 63995 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 367 7 1 4 5.6 CCc1nc(NC(CC)CC)c(OC)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
9969024 64012 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 363 8 1 5 5.1 CCOc1ccc(-c2nc(OC)c(NC(CC)CC)nc2C)c(Cl)c1 10.1021/jm200365y
CHEMBL1807056 64012 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 363 8 1 5 5.1 CCOc1ccc(-c2nc(OC)c(NC(CC)CC)nc2C)c(Cl)c1 10.1021/jm200365y
21916308 93798 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 485 8 0 5 6.7 CCCN(CCc1ccccc1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL247557 93798 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 485 8 0 5 6.7 CCCN(CCc1ccccc1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL4299287 213560 0 None -2 2 Human 8.2 pKi = 8.2 Binding
Displacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1]-PD-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL None None None CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]1CCCCNC(=O)CC[C@@H](NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](C)NC(=O)C(C)(CC(C)C)NC(=O)[C@@H](CCC(N)=O)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](C)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](C)NC(=O)C(CCCC)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(=O)O)NC(C)=O)[C@H](C)O)C(C)C)C(=O)N[C@H](Cc2ccc(NC(=O)[C@@H]3CC(=O)NC(=O)N3)cc2)C(=O)N[C@@H](Cc2ccc(NC(N)=O)cc2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)NC(C)(CC(C)C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL2372922 210313 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(N)=O)[C@@H](C)CC)[C@@H](C)CC 10.1021/jm034180+
20780182 93839 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 435 7 0 5 5.9 CCN(CCC1CC1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL247753 93839 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 435 7 0 5 5.9 CCN(CCC1CC1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
10166565 64323 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 561 8 1 4 8.5 FC(F)(F)CN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181133 64323 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 561 8 1 4 8.5 FC(F)(F)CN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
11598824 71784 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 404 5 0 5 5.0 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CCOC 10.1021/jm049085v
CHEMBL196740 71784 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 404 5 0 5 5.0 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CCOC 10.1021/jm049085v
11660986 140262 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 384 4 0 4 5.2 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL380563 140262 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 384 4 0 4 5.2 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
10157369 115257 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 391 5 1 4 5.6 CCN(CC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
CHEMBL334778 115257 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 391 5 1 4 5.6 CCN(CC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
11610200 71731 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 360 2 0 4 4.9 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1C 10.1021/jm049085v
CHEMBL196594 71731 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 360 2 0 4 4.9 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1C 10.1021/jm049085v
9928790 193555 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 359 9 0 6 4.1 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL526828 193555 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 359 9 0 6 4.1 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
11742775 154775 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2ncccc2C)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL400156 154775 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2ncccc2C)nc1CC 10.1016/j.bmcl.2007.09.008
11067569 203623 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 332 5 2 5 3.5 CC(=O)/C(=N\c1cccc(Cl)c1)NNc1ccccc1[N+](=O)[O-] 10.1021/jm025512y
CHEMBL67121 203623 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 332 5 2 5 3.5 CC(=O)/C(=N\c1cccc(Cl)c1)NNc1ccccc1[N+](=O)[O-] 10.1021/jm025512y
10786789 58500 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 393 5 0 4 5.9 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(C(C)C)cc1SC 10.1021/jm980222w
CHEMBL168341 58500 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 393 5 0 4 5.9 CCN(c1nc(C)cc(C)n1)c1c(Br)cc(C(C)C)cc1SC 10.1021/jm980222w
44443654 94067 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 437 9 1 7 4.6 CCc1nc(Oc2cc(C)ncn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1016/j.bmcl.2007.09.008
CHEMBL248996 94067 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 437 9 1 7 4.6 CCc1nc(Oc2cc(C)ncn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCF 10.1016/j.bmcl.2007.09.008
11474841 78345 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 9 0 5 5.6 CCC[C@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL2093961 78345 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 9 0 5 5.6 CCC[C@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL2110009 78345 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 9 0 5 5.6 CCC[C@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
44352358 18746 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 429 10 1 6 5.5 CCCN(Cc1sc(Nc2ccc(OC)cc2OC)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL127783 18746 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 429 10 1 6 5.5 CCCN(Cc1sc(Nc2ccc(OC)cc2OC)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
44392759 65241 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 393 7 0 4 5.5 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(C)c(C)c(C)c(C)c2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL182705 65241 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 393 7 0 4 5.5 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(C)c(C)c(C)c(C)c2C)c1C 10.1016/j.bmcl.2004.05.072
10299169 132411 0 None - 1 Human 5.3 pKi = 5.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 473 6 1 5 6.5 COC[C@@H]1CCCN1Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL369754 132411 0 None - 1 Human 5.3 pKi = 5.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 473 6 1 5 6.5 COC[C@@H]1CCCN1Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
10297799 18930 0 None - 1 Human 4.3 pKi = 4.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 451 9 1 6 4.9 COCCN(CCOC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
CHEMBL128566 18930 0 None - 1 Human 4.3 pKi = 4.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 451 9 1 6 4.9 COCCN(CCOC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
44305179 203365 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 322 6 0 4 4.6 CCCCN(CC)c1cc(C)nc2c(-c3ccccc3)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL65195 203365 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 322 6 0 4 4.6 CCCCN(CC)c1cc(C)nc2c(-c3ccccc3)c(C)nn12 10.1016/s0960-894x(98)00372-2
44460546 205337 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 416 7 1 3 6.2 Cc1cc(F)ccc1C(Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
CHEMBL79576 205337 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 416 7 1 3 6.2 Cc1cc(F)ccc1C(Nc1ccc(Cl)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
44460368 205651 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 490 6 2 3 6.8 CC(=O)Nc1cccc(C(=O)C(Nc2ccc(Cl)cc2Cl)c2ccccc2Br)c1 10.1021/jm049974i
CHEMBL81912 205651 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 490 6 2 3 6.8 CC(=O)Nc1cccc(C(=O)C(Nc2ccc(Cl)cc2Cl)c2ccccc2Br)c1 10.1021/jm049974i
44407864 75408 0 None - 1 Rat 5.3 pKi = 5.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 394 4 1 4 5.5 Cc1cccc(S(=O)(=O)c2c(C)cc(C)nc2Nc2c(C)cc(C)cc2C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL204014 75408 0 None - 1 Rat 5.3 pKi = 5.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 394 4 1 4 5.5 Cc1cccc(S(=O)(=O)c2c(C)cc(C)nc2Nc2c(C)cc(C)cc2C)c1 10.1016/j.bmcl.2005.10.097
44341902 10168 1 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 348 7 0 3 5.8 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL115928 10168 1 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 348 7 0 3 5.8 CCCN(CCC)c1cc(C)nc2c(-c3ccc(OC)cc3)cccc12 10.1016/s0960-894x(03)00684-x
11418006 75552 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 394 5 1 4 5.5 CCc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
CHEMBL204481 75552 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 394 5 1 4 5.5 CCc1ccc(S(=O)(=O)c2ccc(C)nc2Nc2c(C)cc(C)cc2C)cc1 10.1016/j.bmcl.2005.10.097
44446739 94649 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 488 10 0 5 6.1 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCN(C)CC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL252493 94649 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 488 10 0 5 6.1 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OCCN2CCN(C)CC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
11065415 203426 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 267 4 2 3 3.2 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1C 10.1021/jm025512y
CHEMBL65708 203426 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 267 4 2 3 3.2 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1C 10.1021/jm025512y
11022343 203670 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 281 4 2 3 3.5 CC(=O)/C(=N\c1cccc(C)c1)NNc1ccccc1C 10.1021/jm025512y
CHEMBL67394 203670 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 281 4 2 3 3.5 CC(=O)/C(=N\c1cccc(C)c1)NNc1ccccc1C 10.1021/jm025512y
20780067 67888 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 522 6 0 4 7.4 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CC4CCC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL191052 67888 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 522 6 0 4 7.4 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CC4CCC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
21916146 6492 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 466 8 0 4 6.7 CCCN(CCC1CC1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1082697 6492 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 466 8 0 4 6.7 CCCN(CCC1CC1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
10410573 94380 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 9 1 6 5.5 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(CC)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL250814 94380 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 432 9 1 6 5.5 CCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(CC)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
44587492 193629 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 385 10 0 5 5.5 CCCOc1nc(-c2c(C)cc(C)cc2OC)nc(C)c1N(CCC)CCC 10.1016/j.bmcl.2008.07.063
CHEMBL527030 193629 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 385 10 0 5 5.5 CCCOc1nc(-c2c(C)cc(C)cc2OC)nc(C)c1N(CCC)CCC 10.1016/j.bmcl.2008.07.063
22324332 106977 0 None - 1 Human 6.3 pKi = 6.3 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 359 8 0 6 3.4 CCCN(CCC)c1c(C)nc(-c2c(OC)cccc2OC)n(C)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL315112 106977 0 None - 1 Human 6.3 pKi = 6.3 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 359 8 0 6 3.4 CCCN(CCC)c1c(C)nc(-c2c(OC)cccc2OC)n(C)c1=O 10.1016/s0960-894x(03)00483-9
44392739 64691 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 353 6 1 6 4.0 CCCN(CCC)c1cc(C)nc2c(-c3ncc(O)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL181860 64691 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 353 6 1 6 4.0 CCCN(CCC)c1cc(C)nc2c(-c3ncc(O)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
44443595 172650 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 390 8 1 5 5.9 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(c1ccccc1)C(C)C 10.1016/j.bmcl.2007.09.008
CHEMBL449657 172650 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 390 8 1 5 5.9 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(c1ccccc1)C(C)C 10.1016/j.bmcl.2007.09.008
11046479 103114 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 355 4 2 3 4.8 CC(=O)/C(=N\Nc1ccccc1C(F)(F)F)Nc1cccc(Cl)c1 10.1021/jm025512y
CHEMBL307751 103114 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 355 4 2 3 4.8 CC(=O)/C(=N\Nc1ccccc1C(F)(F)F)Nc1cccc(Cl)c1 10.1021/jm025512y
20780105 68023 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 558 8 0 4 7.8 CC(C)c1ccc(-n2c3ccccc3n3c(CN(CC4CC4)CC4CC4)c(C(F)(F)F)nc23)c(Br)c1 10.1016/j.bmcl.2005.06.028
CHEMBL191366 68023 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 558 8 0 4 7.8 CC(C)c1ccc(-n2c3ccccc3n3c(CN(CC4CC4)CC4CC4)c(C(F)(F)F)nc23)c(Br)c1 10.1016/j.bmcl.2005.06.028
10708209 57512 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 284 4 0 4 3.6 CCN(c1nc(C)cc(C)n1)c1ccc(N(C)C)cc1C 10.1021/jm980222w
CHEMBL166110 57512 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 284 4 0 4 3.6 CCN(c1nc(C)cc(C)n1)c1ccc(N(C)C)cc1C 10.1021/jm980222w
22249007 63998 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 351 6 1 3 5.9 CCc1nc(NC(CC)CC)c(C)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
CHEMBL1807038 63998 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 351 6 1 3 5.9 CCc1nc(NC(CC)CC)c(C)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
18691311 5046 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 457 7 0 6 5.4 CCN(c1nc(C)cc(-c2ccccc2OC)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
CHEMBL10526 5046 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 457 7 0 6 5.4 CCN(c1nc(C)cc(-c2ccccc2OC)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
44392800 132404 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 355 7 1 5 3.5 CCCN(CCO)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL369717 132404 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 355 7 1 5 3.5 CCCN(CCO)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
22249074 63991 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 337 6 1 3 5.6 CCc1nc(NC(CC)CC)cnc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
CHEMBL1807031 63991 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 337 6 1 3 5.6 CCc1nc(NC(CC)CC)cnc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
44460272 205697 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity of compound towards human corticotropin releasing factor (h-CRF1) receptor showed a 2-fold activity in racemic mixtureBinding affinity of compound towards human corticotropin releasing factor (h-CRF1) receptor showed a 2-fold activity in racemic mixture
ChEMBL 442 7 1 3 6.2 Cc1ccc(N[C@@H](C(=O)CCc2ccncc2)c2ccccc2Br)c(Cl)c1 10.1021/jm049974i
CHEMBL82308 205697 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity of compound towards human corticotropin releasing factor (h-CRF1) receptor showed a 2-fold activity in racemic mixtureBinding affinity of compound towards human corticotropin releasing factor (h-CRF1) receptor showed a 2-fold activity in racemic mixture
ChEMBL 442 7 1 3 6.2 Cc1ccc(N[C@@H](C(=O)CCc2ccncc2)c2ccccc2Br)c(Cl)c1 10.1021/jm049974i
44443630 154728 0 None - 1 Human 5.3 pKi = 5.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@@H]1Nc1nc(CC)c(Oc2cc(C)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL399877 154728 0 None - 1 Human 5.3 pKi = 5.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 418 8 1 6 5.2 CCO[C@H]1Cc2ccccc2[C@@H]1Nc1nc(CC)c(Oc2cc(C)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
44392691 66303 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 379 8 0 4 5.1 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1CC 10.1016/j.bmcl.2004.05.072
CHEMBL184851 66303 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 379 8 0 4 5.1 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1CC 10.1016/j.bmcl.2004.05.072
11156095 68974 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 377 7 0 4 5.7 CCCC(CCC)N1CCc2cn(-c3ccccc3OC)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL192288 68974 0 None - 1 Human 7.3 pKi = 7.3 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 377 7 0 4 5.7 CCCC(CCC)N1CCc2cn(-c3ccccc3OC)c3nc(C)cc1c23 10.1021/jm050070m
10835652 119177 0 None - 1 Human 4.3 pKi = 4.3 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 415 7 2 5 5.7 CCc1cccc(CC)c1Nc1nc(C)nc(NCc2ccc(C(F)(F)F)cc2)n1 10.1021/jm960148m
CHEMBL343073 119177 0 None - 1 Human 4.3 pKi = 4.3 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 415 7 2 5 5.7 CCc1cccc(CC)c1Nc1nc(C)nc(NCc2ccc(C(F)(F)F)cc2)n1 10.1021/jm960148m
44389084 122316 0 None - 1 Human 4.3 pKi = 4.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 443 4 1 4 6.9 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN1CCCCC1 10.1016/j.bmcl.2004.10.055
CHEMBL359828 122316 0 None - 1 Human 4.3 pKi = 4.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 443 4 1 4 6.9 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN1CCCCC1 10.1016/j.bmcl.2004.10.055
10164848 21478 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 517 10 0 4 7.8 CCCN(Cc1sc(N(CC)c2ccc(C(C)C)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL131571 21478 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 517 10 0 4 7.8 CCCN(Cc1sc(N(CC)c2ccc(C(C)C)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
3495 1175 28 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(98)00372-2
5311055 1175 28 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(98)00372-2
CHEMBL9946 1175 28 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 364 6 0 4 5.6 CCCCN(c1nc(C)nc2c1c(C)cn2c1c(C)cc(cc1C)C)CC 10.1016/s0960-894x(98)00372-2
136029158 205670 0 None - 1 Human 6.3 pKi = 6.3 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 357 8 1 5 4.7 CCCN(CCC)c1c(O)nc(-c2c(C)cc(C)cc2OC)nc1CC 10.1016/s0960-894x(03)00483-9
CHEMBL82112 205670 0 None - 1 Human 6.3 pKi = 6.3 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 357 8 1 5 4.7 CCCN(CCC)c1c(O)nc(-c2c(C)cc(C)cc2OC)nc1CC 10.1016/s0960-894x(03)00483-9
44392751 122056 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 397 10 0 6 4.5 C=C(c1cc(N(CCC)CC2CC2)nc(C)n1)c1c(OC)cc(OC)cc1OC 10.1016/j.bmcl.2004.05.072
CHEMBL359636 122056 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 397 10 0 6 4.5 C=C(c1cc(N(CCC)CC2CC2)nc(C)n1)c1c(OC)cc(OC)cc1OC 10.1016/j.bmcl.2004.05.072
10206904 122766 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 493 7 1 4 7.5 CN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL360471 122766 0 None - 1 Human 6.3 pKi = 6.3 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 493 7 1 4 7.5 CN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
21916237 93360 0 None - 1 Human 5.3 pKi = 5.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 441 8 1 7 4.0 COCC(COC)NCc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL245506 93360 0 None - 1 Human 5.3 pKi = 5.3 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 441 8 1 7 4.0 COCC(COC)NCc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
44308134 203562 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 460 7 0 6 5.3 CCCN(CCN1CCCCC1)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL66671 203562 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 460 7 0 6 5.3 CCCN(CCN1CCCCC1)c1nc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
44587452 188146 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 327 7 0 4 4.7 CCCN(CCC)c1cnc(-c2c(C)cc(C)cc2OC)nc1C 10.1016/j.bmcl.2008.07.063
CHEMBL498480 188146 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 327 7 0 4 4.7 CCCN(CCC)c1cnc(-c2c(C)cc(C)cc2OC)nc1C 10.1016/j.bmcl.2008.07.063
9797993 102980 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 339 7 1 5 4.5 CCCN(CC1CC1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960149e
CHEMBL306618 102980 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 339 7 1 5 4.5 CCCN(CC1CC1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960149e
9797993 102980 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 339 7 1 5 4.5 CCCN(CC1CC1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
CHEMBL306618 102980 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 339 7 1 5 4.5 CCCN(CC1CC1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm960148m
9797993 102980 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 339 7 1 5 4.5 CCCN(CC1CC1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
CHEMBL306618 102980 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 339 7 1 5 4.5 CCCN(CC1CC1)c1nc(C)nc(Nc2c(C)cc(C)cc2C)n1 10.1021/jm9900117
18672241 64366 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 455 8 1 4 7.0 C=CCN(CC=C)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181280 64366 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 455 8 1 4 7.0 C=CCN(CC=C)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
20780125 123874 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 442 7 0 4 6.0 CCCN(CC1CC1)C(=O)c1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL362706 123874 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 442 7 0 4 6.0 CCCN(CC1CC1)C(=O)c1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
20780058 93328 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 458 6 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)CCc4cccnc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL245297 93328 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 458 6 0 6 5.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN(C)CCc4cccnc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
10062901 170244 1 None - 1 Rat 5.2 pKi = 5.2 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 291 2 0 3 3.6 Cc1cc(C)nc(N(C)c2ccccc2Br)n1 10.1021/jm980222w
CHEMBL444577 170244 1 None - 1 Rat 5.2 pKi = 5.2 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 291 2 0 3 3.6 Cc1cc(C)nc(N(C)c2ccccc2Br)n1 10.1021/jm980222w
10783164 27058 0 None - 1 Human 5.2 pKi = 5.2 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 337 9 1 5 4.2 C=CCN(CC=C)c1nc(C)nc(Nc2c(CC)cccc2CC)n1 10.1021/jm960148m
CHEMBL136519 27058 0 None - 1 Human 5.2 pKi = 5.2 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 337 9 1 5 4.2 C=CCN(CC=C)c1nc(C)nc(Nc2c(CC)cccc2CC)n1 10.1021/jm960148m
20780072 67226 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 476 5 0 4 6.9 Cc1cc(C)c(-n2c3ccccc3n3c(CN(C)Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL187924 67226 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 476 5 0 4 6.9 Cc1cc(C)c(-n2c3ccccc3n3c(CN(C)Cc4ccccc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
11268730 161844 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 370 4 0 5 4.2 CCC(CC)N1CCn2c(=O)n(-c3ccc(Cl)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL414664 161844 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 370 4 0 5 4.2 CCC(CC)N1CCn2c(=O)n(-c3ccc(Cl)cc3)c3nc(C)cc1c32 10.1021/jm050384+
44392764 65199 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 353 7 0 4 4.9 CCCN(CCC)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL182504 65199 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 353 7 0 4 4.9 CCCN(CCC)c1nc(C)nc(C(=O)c2c(C)cc(C)cc2C)c1C 10.1016/j.bmcl.2004.05.072
44443650 94031 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 446 9 1 6 5.9 CCCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(C)cc(C)n2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL248803 94031 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 446 9 1 6 5.9 CCCO[C@H]1Cc2ccccc2[C@H]1Nc1nc(CC)c(Oc2cc(C)cc(C)n2)nc1CC 10.1016/j.bmcl.2007.09.008
11364104 75605 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 502 8 1 6 6.5 COc1cccc(COc2ccc(S(=O)(=O)c3ccc(C)nc3Nc3c(C)cc(C)cc3C)cc2)c1 10.1016/j.bmcl.2005.10.097
CHEMBL204690 75605 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 502 8 1 6 6.5 COc1cccc(COc2ccc(S(=O)(=O)c3ccc(C)nc3Nc3c(C)cc(C)cc3C)cc2)c1 10.1016/j.bmcl.2005.10.097
21916273 6967 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 542 6 0 4 8.1 CCN(Cc1ccc(Cl)c(Cl)c1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1084565 6967 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 542 6 0 4 8.1 CCN(Cc1ccc(Cl)c(Cl)c1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
20780049 148838 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 469 4 0 5 6.6 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCCC4c4ccccc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL394112 148838 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 469 4 0 5 6.6 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCCC4c4ccccc4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
46891010 6436 0 None - 1 Human 5.2 pKi = 5.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 3 0 4 6.0 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCCC(C)C4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082443 6436 0 None - 1 Human 5.2 pKi = 5.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 3 0 4 6.0 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCCC(C)C4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
21916154 122577 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 432 7 0 4 6.3 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ccc(F)cc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
CHEMBL360185 122577 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 432 7 0 4 6.3 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ccc(F)cc3n12)CC1CC1 10.1016/j.bmcl.2005.06.028
44341755 10154 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 412 9 0 4 6.8 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(C)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL115818 10154 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 412 9 0 4 6.8 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(C)cc3Cl)n(CC)nc12 10.1016/s0960-894x(03)00621-8
122193724 123889 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 448 5 0 4 4.8 Cc1cc(N(C)C)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2CCF 10.1016/j.bmcl.2015.10.010
CHEMBL3627731 123889 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 448 5 0 4 4.8 Cc1cc(N(C)C)c2c(n1)N(c1ccc(C(C)C)cc1Br)CC(=O)N2CCF 10.1016/j.bmcl.2015.10.010
44443591 94332 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 376 8 1 5 5.7 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(CC)c1ccccc1 10.1016/j.bmcl.2007.09.008
CHEMBL250617 94332 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 376 8 1 5 5.7 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1NC(CC)c1ccccc1 10.1016/j.bmcl.2007.09.008
10831985 120478 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 354 6 1 7 3.3 CCC(COC)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL354256 120478 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 354 6 1 7 3.3 CCC(COC)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
10788999 57505 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 435 9 0 7 4.6 CCCCN(CC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
CHEMBL166056 57505 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 435 9 0 7 4.6 CCCCN(CC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
10764802 58717 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 424 9 0 6 5.0 CCCN(CCC)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
CHEMBL168497 58717 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 424 9 0 6 5.0 CCCN(CCC)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C(F)(F)F)n1 10.1021/jm980222w
10549365 165695 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 406 7 0 6 4.0 CCN(CC)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL424538 165695 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 406 7 0 6 4.0 CCN(CC)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2Br)n1 10.1021/jm980222w
10228129 7399 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 488 7 0 4 6.8 CCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1086504 7399 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 488 7 0 4 6.8 CCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
21916331 147489 1 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 449 7 0 5 6.3 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12)CC1CCC1 10.1016/j.bmcl.2007.01.008
CHEMBL393044 147489 1 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 449 7 0 5 6.3 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12)CC1CCC1 10.1016/j.bmcl.2007.01.008
44446725 168953 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL438888 168953 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
44446725 168953 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2008.07.063
CHEMBL438888 168953 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 376 7 0 3 6.5 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2008.07.063
44587455 188047 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 465 8 0 5 6.1 CCCN(CCC)c1c(C)nc(-c2c(OC)cc(C(F)(F)F)cc2C(F)(F)F)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL497651 188047 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 465 8 0 5 6.1 CCCN(CCC)c1c(C)nc(-c2c(OC)cc(C(F)(F)F)cc2C(F)(F)F)nc1OC 10.1016/j.bmcl.2008.07.063
11166919 166308 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 417 5 0 4 6.1 CCC(CC)N1CCc2cn(-c3ccc(OC(F)(F)F)cc3C)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL427168 166308 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 417 5 0 4 6.1 CCC(CC)N1CCc2cn(-c3ccc(OC(F)(F)F)cc3C)c3nc(C)cc1c23 10.1021/jm050070m
44384801 132273 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 393 6 0 6 4.0 CCCN(CC1CC1)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00108-0
CHEMBL369700 132273 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 393 6 0 6 4.0 CCCN(CC1CC1)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00108-0
11798114 58807 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 457 9 0 5 6.4 CCCCN(CCCC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168823 58807 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 457 9 0 5 6.4 CCCCN(CCCC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
9910700 59045 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 1 7 4.2 CCC(COC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169416 59045 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 1 7 4.2 CCC(COC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10295219 64013 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 413 9 1 6 5.2 CCc1nc(-c2ccc(OC(F)(F)F)cc2OC)c(OC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1807057 64013 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 413 9 1 6 5.2 CCc1nc(-c2ccc(OC(F)(F)F)cc2OC)c(OC)nc1NC(CC)CC 10.1021/jm200365y
10303191 169275 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 561 8 1 4 8.8 FC(F)(F)CCN(Cc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL441311 169275 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 561 8 1 4 8.8 FC(F)(F)CCN(Cc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
44392781 129671 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 371 6 0 5 5.0 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL367371 129671 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 371 6 0 5 5.0 CCCN(CCC)c1cc(C)nc2c(-c3ncc(C)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
10789145 33091 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 437 9 1 7 4.6 CCOCC(COCC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
CHEMBL141692 33091 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1Displacement of [125I]-tyrosine-ovine-CRF from human Corticotropin releasing factor receptor 1
ChEMBL 437 9 1 7 4.6 CCOCC(COCC)Nc1nc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1021/jm9904351
10142098 6491 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 7 0 4 6.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC4CC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1082696 6491 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 506 7 0 4 6.9 Cc1cc(C)c(-n2c(Cl)cn3c(CN(CCC4CC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
11212114 106391 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 412 9 0 5 5.9 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL3085416 106391 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 412 9 0 5 5.9 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL3139409 106391 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 412 9 0 5 5.9 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
11576870 70572 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 380 4 0 4 5.4 CC[C@H]1Cn2nc(-c3ccc(C)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL194890 70572 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 380 4 0 4 5.4 CC[C@H]1Cn2nc(-c3ccc(C)cc3Cl)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11634953 71917 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 402 5 0 4 6.1 CCCCN1c2cc(C)nc3c(-c4ccc(Cl)cc4Cl)nn(c23)C[C@@H]1CC 10.1021/jm049085v
CHEMBL197197 71917 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 402 5 0 4 6.1 CCCCN1c2cc(C)nc3c(-c4ccc(Cl)cc4Cl)nn(c23)C[C@@H]1CC 10.1021/jm049085v
44305255 102754 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 416 4 0 4 6.5 CCCC1CCCCN1c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL305092 102754 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 416 4 0 4 6.5 CCCC1CCCCN1c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
21916296 147006 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 471 7 0 5 6.3 CCN(CCc1ccccc1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL392655 147006 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 471 7 0 5 6.3 CCN(CCc1ccccc1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3Cl)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
44342084 10026 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 392 8 0 4 5.2 COCCN(CCOC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL115032 10026 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 392 8 0 4 5.2 COCCN(CCOC)c1cc(C)nc2c(-c3c(C)cc(C)cc3C)cccc12 10.1016/s0960-894x(03)00684-x
44396572 123388 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 444 8 1 7 4.5 COCC(Cc1ccccc1)Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL361670 123388 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 444 8 1 7 4.5 COCC(Cc1ccccc1)Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
11477320 70929 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 391 7 0 4 6.0 CCCC(CCC)N1CCc2cn(-c3ccc(OC)cc3C)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL195152 70929 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 391 7 0 4 6.0 CCCC(CCC)N1CCc2cn(-c3ccc(OC)cc3C)c3nc(C)cc1c23 10.1021/jm050070m
9849255 195908 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 510 9 0 8 5.5 COCCN(CCOC)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
CHEMBL559127 195908 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 510 9 0 8 5.5 COCCN(CCOC)c1nc(C)nc2c1sc(=S)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
44392805 64877 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 463 6 0 5 4.9 CCCN(CCC)c1cc(C)nc2c(-c3ncc(I)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL182165 64877 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 463 6 0 5 4.9 CCCN(CCC)c1cc(C)nc2c(-c3ncc(I)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
44392643 64569 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 371 6 0 5 5.0 CCCN(CCC)c1cc(C)nc2c(-c3ncc(Cl)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL181548 64569 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 371 6 0 5 5.0 CCCN(CCC)c1cc(C)nc2c(-c3ncc(Cl)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
10672237 58711 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 475 9 0 7 4.4 COCCN(CCOC)c1nc(C)nc2c1nc(C)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL168476 58711 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 475 9 0 7 4.4 COCCN(CCOC)c1nc(C)nc2c1nc(C)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341816 9553 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 434 9 0 5 5.9 CCCCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112336 9553 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 434 9 0 5 5.9 CCCCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
11339333 63077 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 426 10 0 5 6.3 CCCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL178836 63077 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 426 10 0 5 6.3 CCCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
44388403 166184 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 406 10 0 5 5.9 CCCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL426419 166184 0 None - 1 Human 8.2 pKi = 8.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 406 10 0 5 5.9 CCCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
44352448 18964 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 411 8 1 4 6.5 CCCN(Cc1sc(Nc2c(C)cc(C)cc2C)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL128713 18964 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 411 8 1 4 6.5 CCCN(Cc1sc(Nc2c(C)cc(C)cc2C)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
11188634 125955 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 395 7 0 7 3.7 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(OC)nc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL364892 125955 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 395 7 0 7 3.7 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(OC)nc3)c3nc(C)cc1c32 10.1021/jm050384+
10662222 58505 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 303 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1ccc(OC)cc1SC 10.1021/jm980222w
CHEMBL168359 58505 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 303 5 0 5 4.0 CCN(c1nc(C)cc(C)n1)c1ccc(OC)cc1SC 10.1021/jm980222w
9951620 9581 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 376 6 1 3 5.8 CCCCN(CC)c1cc(C)[nH]c2c(-c3ccc(Cl)cc3Cl)nnc1-2 10.1016/s0960-894x(03)00621-8
CHEMBL112478 9581 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 376 6 1 3 5.8 CCCCN(CC)c1cc(C)[nH]c2c(-c3ccc(Cl)cc3Cl)nnc1-2 10.1016/s0960-894x(03)00621-8
44587454 193162 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 415 10 1 6 4.7 CCCN(CCC)c1c(CC(C)(C)O)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL523074 193162 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 415 10 1 6 4.7 CCCN(CCC)c1c(CC(C)(C)O)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
20780008 7349 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 412 6 0 4 5.3 CCCN(CC1CC1)C(=O)c1c(C)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1086259 7349 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 412 6 0 4 5.3 CCCN(CC1CC1)C(=O)c1c(C)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
20780037 131793 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 422 6 0 4 4.9 CCCN(CC(F)(F)F)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL369341 131793 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 422 6 0 4 4.9 CCCN(CC(F)(F)F)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
44388393 60553 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 9 0 5 5.6 CCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL175902 60553 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 9 0 5 5.6 CCCC(c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
21916323 7090 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 486 4 0 4 6.7 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCC(c5ccccc5)C4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1085088 7090 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 486 4 0 4 6.7 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCC(c5ccccc5)C4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
20780251 64368 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 394 7 0 4 4.8 CCc1nc2n(c1C(=O)N(CC)CCC1CC1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL181287 64368 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 394 7 0 4 4.8 CCc1nc2n(c1C(=O)N(CC)CCC1CC1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780070 127289 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 572 8 0 4 8.2 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCc4ccccc4)CCC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL365858 127289 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 572 8 0 4 8.2 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCc4ccccc4)CCC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
11077161 203490 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 291 4 2 3 3.2 C#Cc1cccc(/N=C(/NNc2ccccc2C)C(C)=O)c1 10.1021/jm025512y
CHEMBL66157 203490 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 291 4 2 3 3.2 C#Cc1cccc(/N=C(/NNc2ccccc2C)C(C)=O)c1 10.1021/jm025512y
9865345 9459 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 392 6 2 5 4.8 CCCC(CO)Nc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL111867 9459 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 392 6 2 5 4.8 CCCC(CO)Nc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
44307655 203686 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 393 8 0 5 5.8 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)nn(CCC)c12 10.1016/s0960-894x(02)00358-x
CHEMBL67483 203686 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 393 8 0 5 5.8 CCCN(CCC)c1nc(C)nc2c(-c3c(C)cc(C)cc3C)nn(CCC)c12 10.1016/s0960-894x(02)00358-x
11222685 69007 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 378 4 0 4 5.4 CCC(CC)N1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL192335 69007 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 378 4 0 4 5.4 CCC(CC)N1CCc2cn(-c3ccc(Cl)cc3C#N)c3nc(C)cc1c23 10.1021/jm050070m
44462209 106189 0 None - 1 Human 6.2 pKi = 6.2 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 409 10 0 6 4.5 CCCN(CCC)c1c(C)nc(-c2c(OC)cccc2OC(F)F)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL313823 106189 0 None - 1 Human 6.2 pKi = 6.2 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 409 10 0 6 4.5 CCCN(CCC)c1c(C)nc(-c2c(OC)cccc2OC(F)F)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
10857993 203563 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 253 4 2 3 2.9 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1 10.1021/jm025512y
CHEMBL66698 203563 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 253 4 2 3 2.9 CC(=O)/C(=N\c1ccccc1)NNc1ccccc1 10.1021/jm025512y
44306462 203041 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 385 9 0 5 4.7 CCCN(c1nccc(-c2c(F)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL63457 203041 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 385 9 0 5 4.7 CCCN(c1nccc(-c2c(F)cc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
44306162 203507 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 413 7 0 3 5.9 CCCN(c1ncc(C)c(-c2ccc(Br)cc2C)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL66249 203507 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 413 7 0 3 5.9 CCCN(c1ncc(C)c(-c2ccc(Br)cc2C)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
10549990 168070 0 None -1 2 Human 7.2 pKi = 7.2 Binding
Compound was tested for the inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneCompound was tested for the inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 418 5 0 5 4.7 CCN(c1nc(C)cc(N2CCOCC2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm990590f
CHEMBL432496 168070 0 None -1 2 Human 7.2 pKi = 7.2 Binding
Compound was tested for the inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membraneCompound was tested for the inhibition of binding of the radioligand, [125 I-Tyr0]-CRF to rat cerebral cortex membrane
ChEMBL 418 5 0 5 4.7 CCN(c1nc(C)cc(N2CCOCC2)n1)c1ccc(C(C)C)cc1Br 10.1021/jm990590f
20780280 64346 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 484 7 0 4 5.6 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)C(F)(F)F)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL181227 64346 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 484 7 0 4 5.6 CCc1nc2n(c1C(=O)N(CC1CC1)CC(F)(F)C(F)(F)F)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
21916183 7581 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 476 7 0 4 6.5 CCCN(CCC(F)(F)F)Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
CHEMBL1087804 7581 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 476 7 0 4 6.5 CCCN(CCC(F)(F)F)Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
11653680 71453 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 374 3 0 4 5.3 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC 10.1021/jm049085v
CHEMBL196146 71453 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 374 3 0 4 5.3 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1CC 10.1021/jm049085v
9887524 166158 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 404 5 0 5 5.0 CCC(COC)N1CCn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c32 10.1021/jm049085v
CHEMBL426283 166158 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 404 5 0 5 5.0 CCC(COC)N1CCn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc1c32 10.1021/jm049085v
44392758 65198 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 399 10 0 7 3.7 CCCN(CC1CC1)c1cc(C)nc(C(=O)c2c(OC)cc(OC)cc2OC)n1 10.1016/j.bmcl.2004.05.072
CHEMBL182500 65198 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 399 10 0 7 3.7 CCCN(CC1CC1)c1cc(C)nc(C(=O)c2c(OC)cc(OC)cc2OC)n1 10.1016/j.bmcl.2004.05.072
10118581 63341 0 None - 1 Human 5.2 pKi = 5.2 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 513 8 1 4 8.7 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CCCCC1 10.1016/j.bmcl.2004.10.055
CHEMBL179416 63341 0 None - 1 Human 5.2 pKi = 5.2 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 513 8 1 4 8.7 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CCCCC1 10.1016/j.bmcl.2004.10.055
11374322 135717 0 None - 1 Rat 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 449 8 1 6 5.6 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCCCC#N)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL372996 135717 0 None - 1 Rat 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 449 8 1 6 5.6 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCCCC#N)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
10575478 168397 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 448 8 1 8 2.9 COCCN(CCO)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL434689 168397 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 448 8 1 8 2.9 COCCN(CCO)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341734 10218 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 446 10 0 4 7.5 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(CCC)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL116010 10218 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 446 10 0 4 7.5 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(CCC)nc12 10.1016/s0960-894x(03)00621-8
44317977 205231 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 412 7 1 3 6.1 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2C)c(C(F)(F)F)c1 10.1021/jm049974i
CHEMBL78721 205231 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 412 7 1 3 6.1 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2C)c(C(F)(F)F)c1 10.1021/jm049974i
11792386 57557 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 353 6 0 7 3.5 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)nc1C 10.1021/jm980224g
CHEMBL166431 57557 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 353 6 0 7 3.5 CCCCN(CC)c1nc(C)nc2c1nnn2-c1c(C)cc(C)nc1C 10.1021/jm980224g
44307784 204080 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 293 4 1 5 3.3 CC(=O)/C(=N\Nc1ccccc1C#N)Oc1cccc(C)c1 10.1021/jm025512y
CHEMBL70143 204080 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 293 4 1 5 3.3 CC(=O)/C(=N\Nc1ccccc1C#N)Oc1cccc(C)c1 10.1021/jm025512y
20780249 64657 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 462 8 0 4 5.7 CCc1nc2n(c1C(=O)N(CCC1CC1)CCC(F)(F)F)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL181823 64657 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 462 8 0 4 5.7 CCc1nc2n(c1C(=O)N(CCC1CC1)CCC(F)(F)F)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
11034476 203803 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 317 5 2 4 3.8 COc1cccc(N/C(=N/Nc2ccccc2Cl)C(C)=O)c1 10.1021/jm025512y
CHEMBL68340 203803 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 317 5 2 4 3.8 COc1cccc(N/C(=N/Nc2ccccc2Cl)C(C)=O)c1 10.1021/jm025512y
20780069 67429 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 522 7 0 4 7.4 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC4CC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL188945 67429 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 522 7 0 4 7.4 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCC4CC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
11759733 203676 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 345 4 2 3 3.9 C#Cc1cccc(/N=C(/NNc2ccccc2C(F)(F)F)C(C)=O)c1 10.1021/jm025512y
CHEMBL67438 203676 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 345 4 2 3 3.9 C#Cc1cccc(/N=C(/NNc2ccccc2C(F)(F)F)C(C)=O)c1 10.1021/jm025512y
10528613 59011 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 476 10 0 8 3.9 COCCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169195 59011 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 476 10 0 8 3.9 COCCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
20780271 122029 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 484 7 0 4 6.1 CCc1nc2n(c1C(=O)N(CCC(F)(F)F)Cc1ccccc1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL359499 122029 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 484 7 0 4 6.1 CCc1nc2n(c1C(=O)N(CCC(F)(F)F)Cc1ccccc1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780285 123911 0 None - 1 Human 5.2 pKi = 5.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 366 7 0 4 4.9 CCCN(Cc1c(C)nc2n1CCN2c1c(C)cc(C)cc1C)CC1CC1 10.1016/j.bmcl.2005.05.117
CHEMBL362799 123911 0 None - 1 Human 5.2 pKi = 5.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 366 7 0 4 4.9 CCCN(Cc1c(C)nc2n1CCN2c1c(C)cc(C)cc1C)CC1CC1 10.1016/j.bmcl.2005.05.117
44266401 4921 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 6 1 6 5.7 CCN(c1nc(C)cc(-c2ccccc2-c2nn[nH]n2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10464 4921 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 477 6 1 6 5.7 CCN(c1nc(C)cc(-c2ccccc2-c2nn[nH]n2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
10204820 115365 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 459 9 0 4 7.2 CCCN(Cc1sc(N(CC)c2c(C)cc(C)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL334976 115365 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 459 9 0 4 7.2 CCCN(Cc1sc(N(CC)c2c(C)cc(C)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
10832559 120424 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 362 2 0 2 5.9 Cc1cc(Cl)c2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL353774 120424 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 362 2 0 2 5.9 Cc1cc(Cl)c2ccn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
21916268 7178 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 6 0 4 6.1 C=C(C)CN(CC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1085518 7178 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 6 0 4 6.1 C=C(C)CN(CC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
44443643 94381 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 458 8 1 6 6.1 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC1CCCC1 10.1016/j.bmcl.2007.09.008
CHEMBL250815 94381 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 458 8 1 6 6.1 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OC1CCCC1 10.1016/j.bmcl.2007.09.008
21916073 7679 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 484 8 0 4 6.8 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
CHEMBL1088626 7679 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 484 8 0 4 6.8 CCCN(CCc1ccccc1)Cc1c(C(F)(F)F)nc2n1CCCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2010.01.127
10113422 64320 0 None - 1 Human 5.2 pKi = 5.2 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 427 4 1 4 6.2 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN1CC=CC1 10.1016/j.bmcl.2004.10.055
CHEMBL181121 64320 0 None - 1 Human 5.2 pKi = 5.2 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 427 4 1 4 6.2 FC(F)(F)c1nc(Nc2c(Cl)cc(Cl)cc2Cl)sc1CN1CC=CC1 10.1016/j.bmcl.2004.10.055
20780167 124477 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 510 7 0 4 7.4 CCCN(CCC(F)(F)F)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL364002 124477 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 510 7 0 4 7.4 CCCN(CCC(F)(F)F)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
10664736 57511 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 338 4 0 4 4.3 CCN(c1nc(C)cc(C)n1)c1ccc(N(C)C)cc1C(F)(F)F 10.1021/jm980222w
CHEMBL166109 57511 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 338 4 0 4 4.3 CCN(c1nc(C)cc(C)n1)c1ccc(N(C)C)cc1C(F)(F)F 10.1021/jm980222w
9803991 168684 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 453 7 0 5 6.5 CCCCN(Cc1ccncc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL436564 168684 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 453 7 0 5 6.5 CCCCN(Cc1ccncc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
20780287 62508 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 406 7 0 4 4.8 CCc1nc2n(c1C(=O)N(CC1CC1)CC1CC1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL178165 62508 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 406 7 0 4 4.8 CCc1nc2n(c1C(=O)N(CC1CC1)CC1CC1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
53309402 63990 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 364 7 0 2 6.6 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1CC(CC)CC 10.1021/jm200365y
CHEMBL1807030 63990 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 364 7 0 2 6.6 CCc1nc(-c2ccc(Cl)cc2Cl)c(CC)nc1CC(CC)CC 10.1021/jm200365y
12982784 15498 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 322 6 0 4 4.6 CCCN(CCC)c1cc(C)nc2c(-c3ccccc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL121614 15498 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 322 6 0 4 4.6 CCCN(CCC)c1cc(C)nc2c(-c3ccccc3)c(C)nn12 10.1016/j.bmcl.2004.05.019
21916111 6490 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 440 7 0 4 6.3 CCCN(CCC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1082686 6490 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 440 7 0 4 6.3 CCCN(CCC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
44305545 100705 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 362 5 1 4 5.5 CCCCNc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL292484 100705 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 362 5 1 4 5.5 CCCCNc1cc(C)nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
10739909 120577 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 402 6 1 6 4.6 CCCCNc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL354579 120577 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 402 6 1 6 4.6 CCCCNc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
11450550 130133 0 None - 1 Human 6.2 pKi = 6.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 336 7 0 5 4.2 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(C)CC 10.1021/jm049339c
CHEMBL367789 130133 0 None - 1 Human 6.2 pKi = 6.2 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 336 7 0 5 4.2 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(C)CC 10.1021/jm049339c
10991736 203735 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 351 5 2 4 4.1 COc1cccc(N/C(=N/Nc2ccccc2C(F)(F)F)C(C)=O)c1 10.1021/jm025512y
CHEMBL67785 203735 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 351 5 2 4 4.1 COc1cccc(N/C(=N/Nc2ccccc2C(F)(F)F)C(C)=O)c1 10.1021/jm025512y
44385629 61297 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 413 8 0 8 2.5 COCCN(CCOC)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00108-0
CHEMBL176707 61297 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 413 8 0 8 2.5 COCCN(CCOC)c1nc(C)nc2c1n(C)c(=O)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00108-0
44462088 205909 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 371 8 0 5 4.3 CCCN(CCC)c1c(CC)nc(-c2c(C)cc(C)cc2OC)n(C)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL84007 205909 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 371 8 0 5 4.3 CCCN(CCC)c1c(CC)nc(-c2c(C)cc(C)cc2OC)n(C)c1=O 10.1016/s0960-894x(03)00483-9
10500067 57835 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 381 9 0 7 3.8 CCCN(CCC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C)n1 10.1021/jm980222w
CHEMBL167095 57835 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 381 9 0 7 3.8 CCCN(CCC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C)n1 10.1021/jm980222w
10832987 58168 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 370 9 0 6 4.3 CCCN(CCC)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C)n1 10.1021/jm980222w
CHEMBL168169 58168 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 370 9 0 6 4.3 CCCN(CCC)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C)n1 10.1021/jm980222w
44341680 111042 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 432 8 0 4 7.0 CCCCN(c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12)C(CC)CC 10.1016/s0960-894x(03)00622-x
CHEMBL326284 111042 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 432 8 0 4 7.0 CCCCN(c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12)C(CC)CC 10.1016/s0960-894x(03)00622-x
44446731 94868 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 400 7 0 3 6.5 COc1cc(C)cc(C)c1-c1nc(C)c(N(CC2CC2)CC2CC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253914 94868 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 400 7 0 3 6.5 COc1cc(C)cc(C)c1-c1nc(C)c(N(CC2CC2)CC2CC2)c2ccccc12 10.1016/j.bmcl.2007.12.050
20780066 66903 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 508 6 0 4 7.0 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CC4CC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL186479 66903 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 508 6 0 4 7.0 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CC4CC4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
10503714 57438 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 449 8 0 8 3.4 COCC(COC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL165478 57438 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 449 8 0 8 3.4 COCC(COC)Oc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
10740327 59003 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 410 8 0 6 4.4 COCCN(CCOC)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL169083 59003 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 410 8 0 6 4.4 COCCN(CCOC)c1nc(C)nc2c1c(C)c(C)n2-c1c(C)cc(C)cc1C 10.1021/jm980224g
10712065 59022 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 338 5 1 6 4.0 CCCC(C)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL169280 59022 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 338 5 1 6 4.0 CCCC(C)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL1077301 208491 0 None 12 2 Human 8.1 pKi = 8.1 Binding
Binding affinity of the receptor corticotropin releasing factor receptor with peptidic agonistsBinding affinity of the receptor corticotropin releasing factor receptor with peptidic agonists
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CO)[C@@H](C)CC)[C@@H](C)O)C(C)C)[C@@H](C)O)C(=O)N[C@@H](C)C(N)=O 10.1021/jm990590f
53310132 63942 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 411 9 1 5 5.8 CCc1nc(-c2ccc(OC(F)(F)F)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806730 63942 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 411 9 1 5 5.8 CCc1nc(-c2ccc(OC(F)(F)F)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
11751120 133624 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 406 6 0 4 6.2 CCCC(CCC)N1CCc2cn(-c3ccc(C#N)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL371407 133624 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 406 6 0 4 6.2 CCCC(CCC)N1CCc2cn(-c3ccc(C#N)cc3Cl)c3nc(C)cc1c23 10.1021/jm050070m
CHEMBL429560 213540 0 None -2 2 Human 8.1 pKi = 8.1 Binding
Binding affinity of the receptor corticotropin releasing factor receptor with peptidic agonistsBinding affinity of the receptor corticotropin releasing factor receptor with peptidic agonists
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H]1CCCN1C(=O)CNC(=O)[C@@H](N)CCC(N)=O)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)C(N)=O 10.1021/jm990590f
122193725 123965 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 476 7 0 4 5.6 CCN(CC)c1cc(C)nc2c1N(CCF)C(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
CHEMBL3628744 123965 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation countingDisplacement of [125I]-Tyr0-sauvagine from human CRF1 receptor expressed in HEK293T cells after 2 hrs by scintillation counting
ChEMBL 476 7 0 4 5.6 CCN(CC)c1cc(C)nc2c1N(CCF)C(=O)CN2c1ccc(C(C)C)cc1Br 10.1016/j.bmcl.2015.10.010
18449319 63941 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 357 9 1 5 4.9 CCc1nc(-c2ccc(OC)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806729 63941 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 357 9 1 5 4.9 CCc1nc(-c2ccc(OC)cc2OC)c(CC)nc1NC(CC)CC 10.1021/jm200365y
11305354 123829 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCCC(c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
CHEMBL362453 123829 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 444 10 0 5 6.4 CCCCC(c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1 10.1021/jm049339c
11450996 122255 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 351 6 0 5 4.7 CCCN(CCC)c1cc(C)nc2c(-c3cnc(C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL359784 122255 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 351 6 0 5 4.7 CCCN(CCC)c1cc(C)nc2c(-c3cnc(C)cc3C)c(C)nn12 10.1021/jm040058e
9957619 59163 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 498 8 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(Br)cc1Br 10.1021/jm980224g
CHEMBL169955 59163 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 498 8 0 8 3.1 COCCN(CCOC)c1nc(C)nc2c1nnn2-c1ccc(Br)cc1Br 10.1021/jm980224g
9910700 59045 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 1 7 4.2 CCC(COC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169416 59045 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 1 7 4.2 CCC(COC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
9932463 165696 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 430 7 0 6 5.0 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL424539 165696 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 430 7 0 6 5.0 CCCCN(CC)c1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44387042 166116 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 459 7 0 6 4.9 CCCN(CCC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL426044 166116 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 459 7 0 6 4.9 CCCN(CCC)c1nc(C)nc2c1n(C)c(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
10690278 59167 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 366 7 1 6 4.8 CCCCC(CC)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
CHEMBL169979 59167 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 366 7 1 6 4.8 CCCCC(CC)Nc1nc(C)nc2c1nnn2-c1c(C)cc(C)cc1C 10.1021/jm980224g
53310275 63976 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 355 8 1 5 4.6 CCc1nc(-c2cnc(C)cc2N(C)C)c(CC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1806957 63976 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 355 8 1 5 4.6 CCc1nc(-c2cnc(C)cc2N(C)C)c(CC)nc1NC(CC)CC 10.1021/jm200365y
44352447 118472 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 603 8 1 4 7.8 CCCN(Cc1sc(Nc2c(Br)cc(Br)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL341313 118472 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 603 8 1 4 7.8 CCCN(Cc1sc(Nc2c(Br)cc(Br)cc2Br)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
44266496 98515 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 459 5 0 3 7.6 CCN(c1nc(C)cc(-c2cccc3ccccc23)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL276184 98515 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 459 5 0 3 7.6 CCN(c1nc(C)cc(-c2cccc3ccccc23)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
22249028 63943 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 371 10 1 5 5.3 CCOc1ccc(-c2nc(CC)c(NC(CC)CC)nc2CC)c(OC)c1 10.1021/jm200365y
CHEMBL1806731 63943 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 371 10 1 5 5.3 CCOc1ccc(-c2nc(CC)c(NC(CC)CC)nc2CC)c(OC)c1 10.1021/jm200365y
16730517 93576 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 451 7 0 5 6.0 CCN(CCc1ccccc1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
CHEMBL246501 93576 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 451 7 0 5 6.0 CCN(CCc1ccccc1)Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12 10.1016/j.bmcl.2007.01.008
3520 3267 54 None 1 2 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm050070m
9821250 3267 54 None 1 2 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm050070m
CHEMBL309138 3267 54 None 1 2 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cellsInhibition of [125I]sauvagine binding to corticotropin releasing factor receptor 1 expressed in LtK- cells
ChEMBL 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10.1021/jm050070m
11710664 69674 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 380 4 0 4 5.4 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3C)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL193522 69674 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 380 4 0 4 5.4 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3C)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11560105 71560 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 386 3 0 4 5.3 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3C[C@H](C)N2CC1CC1 10.1021/jm049085v
CHEMBL196307 71560 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 386 3 0 4 5.3 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3C[C@H](C)N2CC1CC1 10.1021/jm049085v
11525846 71824 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 442 5 0 4 6.6 CC[C@H]1Cn2nc(-c3ccc(C(C)C)cc3C(F)(F)F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL196879 71824 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 442 5 0 4 6.6 CC[C@H]1Cn2nc(-c3ccc(C(C)C)cc3C(F)(F)F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11691278 133138 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 468 4 0 4 6.5 CC[C@H]1Cn2nc(-c3ccc(C(F)(F)F)cc3C(F)(F)F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL370346 133138 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 468 4 0 4 6.5 CC[C@H]1Cn2nc(-c3ccc(C(F)(F)F)cc3C(F)(F)F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
11524791 135226 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 430 5 0 5 5.4 CC[C@H]1Cn2nc(-c3ccc(OC)cc3C(F)(F)F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
CHEMBL372365 135226 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 430 5 0 5 5.4 CC[C@H]1Cn2nc(-c3ccc(OC)cc3C(F)(F)F)c3nc(C)cc(c32)N1CC1CC1 10.1021/jm049085v
44341809 10219 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 414 9 0 5 6.0 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(OC)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL116011 10219 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 414 9 0 5 6.0 CCCCN(CCCC)c1cc(C)nc2c(-c3ccc(OC)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
10573028 31313 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)n1 10.1021/jm960149e
CHEMBL140175 31313 0 None - 1 Human 7.2 pKi = 7.2 Binding
Inhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 dosesInhibition of [125I]CRF binding to human Corticotropin releasing factor receptor 1 tested at 6-12 doses
ChEMBL 398 7 1 4 6.1 CCCN(CC1CC1)c1cc(C)nc(Nc2c(Cl)cc(Cl)cc2Cl)n1 10.1021/jm960149e
44267068 168928 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL 1428 40 17 18 -1.7 CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)C(CCCCC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N1)C(C)C)[C@@H](C)CC)C(N)=O 10.1021/jm034180+
CHEMBL438724 168928 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL 1428 40 17 18 -1.7 CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)C(CCCCC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N1)C(C)C)[C@@H](C)CC)C(N)=O 10.1021/jm034180+
44306535 162683 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 409 9 0 7 4.7 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C1(c2ccoc2)CC1 10.1016/j.bmcl.2004.02.053
CHEMBL417033 162683 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 409 9 0 7 4.7 CCCN(c1nccc(-c2c(OC)cc(OC)cc2OC)n1)C1(c2ccoc2)CC1 10.1016/j.bmcl.2004.02.053
20780050 93912 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 483 5 0 5 6.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCC(Cc5ccccc5)C4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL248162 93912 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 483 5 0 5 6.3 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCC(Cc5ccccc5)C4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
20780052 93913 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 497 6 0 5 6.7 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCC(CCc5ccccc5)C4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL248163 93913 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 497 6 0 5 6.7 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCC(CCc5ccccc5)C4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
20780120 67225 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 456 7 0 4 6.8 CCCCN(CC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL187923 67225 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 456 7 0 4 6.8 CCCCN(CC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
22249115 63993 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 371 6 1 3 6.3 CCc1nc(NC(CC)CC)c(Cl)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
CHEMBL1807033 63993 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 371 6 1 3 6.3 CCc1nc(NC(CC)CC)c(Cl)nc1-c1ccc(Cl)cc1Cl 10.1021/jm200365y
44443570 154773 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 342 9 0 5 4.7 CCCN(CCC)c1nc(CC)c(Oc2cc(C)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
CHEMBL400154 154773 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 342 9 0 5 4.7 CCCN(CCC)c1nc(CC)c(Oc2cc(C)ccn2)nc1CC 10.1016/j.bmcl.2007.09.008
22324340 206066 0 None - 1 Human 7.1 pKi = 7.1 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 355 7 0 4 4.8 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2C)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL85416 206066 0 None - 1 Human 7.1 pKi = 7.1 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 355 7 0 4 4.8 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2C)n(CC)c1=O 10.1016/s0960-894x(03)00483-9
44337493 109785 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 338 7 0 4 4.5 CCCN(c1nc(-c2ccc(C)cc2C)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL323257 109785 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 338 7 0 4 4.5 CCCN(c1nc(-c2ccc(C)cc2C)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
22324337 164402 0 None - 1 Human 6.1 pKi = 6.1 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 387 10 0 6 4.3 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(CCC)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL421334 164402 0 None - 1 Human 6.1 pKi = 6.1 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 387 10 0 6 4.3 CCCN(CCC)c1c(C)nc(-c2ccc(OC)cc2OC)n(CCC)c1=O 10.1016/s0960-894x(03)00483-9
10644018 57584 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 387 2 0 3 5.7 Cc1cc(Cl)c2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
CHEMBL166732 57584 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 387 2 0 3 5.7 Cc1cc(Cl)c2c(C#N)cn(-c3ccc(C(C)C)cc3Br)c2n1 10.1021/jm980223o
44352454 116862 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 431 8 1 4 6.8 CCCN(Cc1sc(Nc2c(C)cc(Cl)cc2C)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL338154 116862 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 431 8 1 4 6.8 CCCN(Cc1sc(Nc2c(C)cc(Cl)cc2C)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
20780281 168253 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 448 7 0 4 5.3 CCc1nc2n(c1C(=O)N(CCC(F)(F)F)CC1CC1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL433768 168253 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 448 7 0 4 5.3 CCc1nc2n(c1C(=O)N(CCC(F)(F)F)CC1CC1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
10277887 64308 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 485 8 1 4 7.9 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CCC1 10.1016/j.bmcl.2004.10.055
CHEMBL181075 64308 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 485 8 1 4 7.9 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CCC1 10.1016/j.bmcl.2004.10.055
44317964 104156 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 428 7 1 3 5.9 O=C(CCc1ccncc1)C(Nc1ccccc1Cl)c1ccccc1Br 10.1021/jm049974i
CHEMBL309546 104156 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 428 7 1 3 5.9 O=C(CCc1ccncc1)C(Nc1ccccc1Cl)c1ccccc1Br 10.1021/jm049974i
20780269 130669 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 380 7 0 4 4.6 C=CCN(CCC)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL368245 130669 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 380 7 0 4 4.6 C=CCN(CCC)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780071 125805 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 558 7 0 4 7.8 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCc4ccccc4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
CHEMBL364809 125805 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 558 7 0 4 7.8 Cc1cc(C)c(-n2c3ccccc3n3c(CN(CCc4ccccc4)CC(F)(F)F)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2005.06.028
20780139 67455 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 496 6 0 4 7.0 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC(F)(F)F 10.1016/j.bmcl.2005.06.028
CHEMBL189115 67455 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 496 6 0 4 7.0 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC(F)(F)F 10.1016/j.bmcl.2005.06.028
20780138 122358 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 546 7 0 4 7.6 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC(F)(F)C(F)(F)F 10.1016/j.bmcl.2005.06.028
CHEMBL360000 122358 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 546 7 0 4 7.6 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12)CC(F)(F)C(F)(F)F 10.1016/j.bmcl.2005.06.028
20780278 66084 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 434 7 0 4 5.5 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(Cl)cc1Cl 10.1016/j.bmcl.2005.05.117
CHEMBL183824 66084 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 434 7 0 4 5.5 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(Cl)cc1Cl 10.1016/j.bmcl.2005.05.117
11375414 75589 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 497 7 1 6 6.3 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCc3cccc(C#N)c3)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL204657 75589 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 497 7 1 6 6.3 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)c2ccc(OCc3cccc(C#N)c3)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
44317759 205580 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 390 8 1 3 6.0 C=Cc1ccccc1C(Nc1ccc(C)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
CHEMBL81376 205580 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 390 8 1 3 6.0 C=Cc1ccccc1C(Nc1ccc(C)cc1Cl)C(=O)CCc1ccncc1 10.1021/jm049974i
44587373 187990 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 385 10 0 5 5.4 CCCc1nc(-c2c(C)cc(C)cc2OC)nc(OC)c1N(CCC)CCC 10.1016/j.bmcl.2008.07.063
CHEMBL497287 187990 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 385 10 0 5 5.4 CCCc1nc(-c2c(C)cc(C)cc2OC)nc(OC)c1N(CCC)CCC 10.1016/j.bmcl.2008.07.063
21916339 7282 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 422 3 0 4 5.5 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CC=CCC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1086015 7282 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 422 3 0 4 5.5 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CC=CCC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
46890890 6999 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 475 6 0 5 5.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)CCc4ccncc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1084722 6999 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 475 6 0 5 5.8 Cc1cc(C)c(-n2c(Cl)cn3c(CN(C)CCc4ccncc4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
44307855 203662 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 357 6 0 5 4.6 CCCN(CCC)c1nc(C)nc2c(-c3ccccc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
CHEMBL67360 203662 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cellsDisplacement of [125I]-sauvagine from Corticotropin releasing factor receptor 1 endogenously expressed in IMR-32 human neuroblastoma cells
ChEMBL 357 6 0 5 4.6 CCCN(CCC)c1nc(C)nc2c(-c3ccccc3Cl)n(C)nc12 10.1016/s0960-894x(02)00358-x
44305202 202856 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 356 6 0 4 5.3 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL62533 202856 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 356 6 0 4 5.3 CCCCN(CC)c1cc(C)nc2c(-c3ccc(Cl)cc3)c(C)nn12 10.1016/s0960-894x(98)00372-2
20780250 63359 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 408 8 0 4 5.2 CCCN(CCC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL179499 63359 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 408 8 0 4 5.2 CCCN(CCC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
18672270 123328 0 None - 1 Human 6.1 pKi = 6.1 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 497 8 1 5 7.9 CCCN(Cc1ccco1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL361647 123328 0 None - 1 Human 6.1 pKi = 6.1 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 497 8 1 5 7.9 CCCN(Cc1ccco1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
20780117 67771 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 518 8 0 4 8.0 CCCCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL190823 67771 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 518 8 0 4 8.0 CCCCN(Cc1ccccc1)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c3ccccc3n12 10.1016/j.bmcl.2005.06.028
44307783 204079 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 309 5 1 6 3.0 COc1cccc(O/C(=N/Nc2ccccc2C#N)C(C)=O)c1 10.1021/jm025512y
CHEMBL70142 204079 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 309 5 1 6 3.0 COc1cccc(O/C(=N/Nc2ccccc2C#N)C(C)=O)c1 10.1021/jm025512y
44392723 123708 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 423 8 0 7 3.8 COCCN(CCOC)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL362203 123708 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 423 8 0 7 3.8 COCCN(CCOC)c1cc(C)nc2c(-c3ncc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.056
21916321 7322 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 440 7 0 4 6.3 CCCCN(CC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
CHEMBL1086142 7322 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 440 7 0 4 6.3 CCCCN(CC)Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12 10.1016/j.bmcl.2010.04.094
18691321 208114 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 452 6 0 4 6.6 CCN(c1nc(C)cc(-c2ccccc2N(C)C)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL9794 208114 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 452 6 0 4 6.6 CCN(c1nc(C)cc(-c2ccccc2N(C)C)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
44392801 122524 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 353 7 1 4 4.4 CCCN(CC1CC1)c1cc(C(O)c2c(C)cc(C)cc2C)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL360128 122524 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 353 7 1 4 4.4 CCCN(CC1CC1)c1cc(C(O)c2c(C)cc(C)cc2C)nc(C)n1 10.1016/j.bmcl.2004.05.072
10666432 120860 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 362 2 0 2 5.9 Cc1cc(Cl)nc2c1ccn2-c1ccc(C(C)C)cc1Br 10.1021/jm980223o
CHEMBL355882 120860 0 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 362 2 0 2 5.9 Cc1cc(Cl)nc2c1ccn2-c1ccc(C(C)C)cc1Br 10.1021/jm980223o
12967652 64591 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 507 8 1 4 7.9 CCN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
CHEMBL181662 64591 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 507 8 1 4 7.9 CCN(CCc1ccccc1)Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F 10.1016/j.bmcl.2004.10.055
11703243 124141 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 360 2 0 4 4.9 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3CCN2C(C)C 10.1021/jm049085v
CHEMBL363394 124141 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 360 2 0 4 4.9 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3CCN2C(C)C 10.1021/jm049085v
11706059 124334 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 388 3 0 4 5.7 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1C(C)C 10.1021/jm049085v
CHEMBL363616 124334 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 388 3 0 4 5.7 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1C(C)C 10.1021/jm049085v
11516283 133627 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 372 3 0 4 4.9 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3CCN2CC1CC1 10.1021/jm049085v
CHEMBL371453 133627 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 372 3 0 4 4.9 Cc1cc2c3c(n1)c(-c1ccc(Cl)cc1Cl)nn3CCN2CC1CC1 10.1021/jm049085v
11602680 71822 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 346 2 1 4 4.9 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1 10.1021/jm049085v
CHEMBL196873 71822 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagineBinding affinity for human corticotropin releasing factor receptor 1 expressed in LtK- cells using [125I]sauvagine
ChEMBL 346 2 1 4 4.9 CC[C@H]1Cn2nc(-c3ccc(Cl)cc3Cl)c3nc(C)cc(c32)N1 10.1021/jm049085v
11474047 125524 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 366 5 0 6 3.5 CCC(CC)N1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL364680 125524 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 366 5 0 6 3.5 CCC(CC)N1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
10622647 120800 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 432 9 0 5 5.5 CCCCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)=O)cc2Br)n1 10.1021/jm980222w
CHEMBL355544 120800 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 432 9 0 5 5.5 CCCCN(CC)c1cc(C)nc(N(CC)c2ccc(C(C)=O)cc2Br)n1 10.1021/jm980222w
10548743 164983 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 395 10 0 7 4.2 CCCCN(CCC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C)n1 10.1021/jm980222w
CHEMBL422555 164983 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 395 10 0 7 4.2 CCCCN(CCC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C)n1 10.1021/jm980222w
10571912 169452 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 381 9 0 7 3.8 CCCCN(CC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C)n1 10.1021/jm980222w
CHEMBL442773 169452 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 381 9 0 7 3.8 CCCCN(CC#N)c1nc(C)nc(N(CC)c2ccc(N(C)C)cc2C)n1 10.1021/jm980222w
44381468 120442 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 445 8 1 6 5.2 CCC(CCOC)Nc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL353891 120442 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 445 8 1 6 5.2 CCC(CCOC)Nc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
23068426 64004 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 367 7 1 4 5.6 CCc1nc(-c2ccc(Cl)cc2Cl)c(OC)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1807048 64004 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 367 7 1 4 5.6 CCc1nc(-c2ccc(Cl)cc2Cl)c(OC)nc1NC(CC)CC 10.1021/jm200365y
9891049 7501 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 474 6 0 4 6.1 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN(CC2CC2)CC(F)(F)F)c(C)c1 10.1016/j.bmcl.2010.01.127
CHEMBL1087165 7501 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cellsDisplacement of [125I]Tyr-o-CRF from human CRFR1 expressed in human IMR32 cells
ChEMBL 474 6 0 4 6.1 Cc1cc(C)c(N2CCCn3c2nc(C(F)(F)F)c3CN(CC2CC2)CC(F)(F)F)c(C)c1 10.1016/j.bmcl.2010.01.127
44446726 94834 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 476 11 0 3 7.5 CCCN(CCC)c1c(C)nc(-c2c(CC(F)F)cc(CC(F)F)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253699 94834 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 476 11 0 3 7.5 CCCN(CCC)c1c(C)nc(-c2c(CC(F)F)cc(CC(F)F)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
44587456 188048 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 344 7 0 5 4.7 CCC(CC)Oc1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL497652 188048 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 344 7 0 5 4.7 CCC(CC)Oc1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
127033836 138627 0 None -1 2 Human 8.1 pKi = 8.1 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3848 124 56 50 -13.2 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
CHEMBL3775830 138627 0 None -1 2 Human 8.1 pKi = 8.1 Binding
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assayDisplacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay
ChEMBL 3848 124 56 50 -13.2 CCCCC(NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C)NC(=O)C(CCCC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N1)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@H](C)C(=O)N[C@H](C(N)=O)[C@@H](C)CC 10.1021/acs.jmedchem.5b00926
44341814 110664 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 422 8 0 6 4.4 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL325918 110664 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 422 8 0 6 4.4 COCCN(CCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
21916322 152819 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 429 7 0 5 5.9 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CCC1 10.1016/j.bmcl.2007.01.008
CHEMBL397389 152819 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 429 7 0 5 5.9 CCCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CCC1 10.1016/j.bmcl.2007.01.008
21916270 6394 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 480 6 0 4 6.5 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC(F)(F)F 10.1016/j.bmcl.2010.04.094
CHEMBL1082302 6394 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 480 6 0 4 6.5 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC(F)(F)F 10.1016/j.bmcl.2010.04.094
44266431 4477 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 485 6 0 3 8.2 CCN(c1nc(C)cc(-c2ccccc2-c2ccccc2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10189 4477 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 485 6 0 3 8.2 CCN(c1nc(C)cc(-c2ccccc2-c2ccccc2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
22249051 64002 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 369 7 1 5 5.1 CCC(CC)Nc1nc(OC)c(-c2ccc(Cl)cc2Cl)nc1OC 10.1021/jm200365y
CHEMBL1807042 64002 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 369 7 1 5 5.1 CCC(CC)Nc1nc(OC)c(-c2ccc(Cl)cc2Cl)nc1OC 10.1021/jm200365y
20780048 148579 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 469 4 0 5 6.2 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCC(c5ccccc5)C4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
CHEMBL393901 148579 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 469 4 0 5 6.2 Cc1cc(C)c(-n2c3ncccc3n3c(CN4CCC(c5ccccc5)C4)c(C)nc23)c(Cl)c1 10.1016/j.bmcl.2007.01.008
9824147 162719 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 432 8 0 8 4.5 COCCN(CCOC)c1nc(C)nc2c1sc(=S)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
CHEMBL417091 162719 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 432 8 0 8 4.5 COCCN(CCOC)c1nc(C)nc2c1sc(=S)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
9869432 18846 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 471 8 1 4 7.5 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
CHEMBL128100 18846 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 471 8 1 4 7.5 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2003.08.055
44347436 16376 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 450 7 0 5 5.4 CCCN(CC1CC1)c1cc([S+](C)[O-])nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.019
CHEMBL122960 16376 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to the cloned human corticotropin releasing factor receptor 1Binding affinity to the cloned human corticotropin releasing factor receptor 1
ChEMBL 450 7 0 5 5.4 CCCN(CC1CC1)c1cc([S+](C)[O-])nc2c(-c3ccc(Cl)cc3Cl)c(C)nn12 10.1016/j.bmcl.2004.05.019
15490817 98558 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 495 6 0 5 6.4 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
CHEMBL276599 98558 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 495 6 0 5 6.4 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
22249156 63999 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 351 6 1 3 5.9 CCc1nc(-c2ccc(Cl)cc2Cl)c(C)nc1NC(CC)CC 10.1021/jm200365y
CHEMBL1807039 63999 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from human CRF-1 receptor expressed in human IMR-32 cells after 2 hrs by scintillation counting
ChEMBL 351 6 1 3 5.9 CCc1nc(-c2ccc(Cl)cc2Cl)c(C)nc1NC(CC)CC 10.1021/jm200365y
9869432 18846 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 471 8 1 4 7.5 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
CHEMBL128100 18846 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 471 8 1 4 7.5 CCCN(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)CC1CC1 10.1016/j.bmcl.2004.10.055
11235359 66288 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 414 6 0 6 5.3 CCCN(c1ccccc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL184752 66288 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 414 6 0 6 5.3 CCCN(c1ccccc1)c1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
44341733 9917 1 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 352 6 0 2 6.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)cccc12 10.1016/s0960-894x(03)00684-x
CHEMBL114419 9917 1 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 352 6 0 2 6.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)cccc12 10.1016/s0960-894x(03)00684-x
44341456 110685 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 496 9 0 5 7.1 CCCCN(CCc1ccc(OC)cc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL325996 110685 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 496 9 0 5 7.1 CCCCN(CCc1ccc(OC)cc1)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)n(C)nc12 10.1016/s0960-894x(03)00621-8
11383809 5371 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 8 0 4 5.7 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(CC)n1)C(C1CC1)C1CC1 10.1021/jm049339c
CHEMBL106972 5371 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 8 0 4 5.7 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(CC)n1)C(C1CC1)C1CC1 10.1021/jm049339c
11383809 5371 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 392 8 0 4 5.7 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(CC)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL106972 5371 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 392 8 0 4 5.7 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(CC)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
9998456 27431 0 None - 1 Human 5.1 pKi = 5.1 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 357 9 1 7 3.6 CCCN(CC1CC1)c1nc(C)nc(Nc2ccc(OC)cc2OC)n1 10.1021/jm960148m
CHEMBL136828 27431 0 None - 1 Human 5.1 pKi = 5.1 Binding
Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1Inhibition of [125I]CRF binding to human corticotropin releasing factor receptor 1
ChEMBL 357 9 1 7 3.6 CCCN(CC1CC1)c1nc(C)nc(Nc2ccc(OC)cc2OC)n1 10.1021/jm960148m
44315525 104190 0 None - 1 Human 5.1 pKi = 5.1 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 387 10 1 8 3.6 CCCN(CC1CC1)c1nc(C)nc(Nc2c(OC)cc(OC)cc2OC)n1 10.1021/jm9900117
CHEMBL309789 104190 0 None - 1 Human 5.1 pKi = 5.1 Binding
Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.Inhibition of [125I]CRH binding to human Corticotropin releasing factor receptor 1.
ChEMBL 387 10 1 8 3.6 CCCN(CC1CC1)c1nc(C)nc(Nc2c(OC)cc(OC)cc2OC)n1 10.1021/jm9900117
CHEMBL413613 213078 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.Binding affinity at human CRF1 receptor (CRFR1) on HeLA cell membranes.
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)=O)NC(=O)[C@@H]1CCCCNC(=O)CC[C@@H](NC(C)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N1)[C@@H](C)CC)C(N)=O 10.1021/jm034180+
44341463 110419 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 356 6 0 4 5.2 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)n(C)nc12 10.1016/s0960-894x(03)00621-8
CHEMBL324495 110419 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cellsBinding affinity to the human corticotropin releasing factor receptor 1 expressed in HEK273 cells
ChEMBL 356 6 0 4 5.2 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)n(C)nc12 10.1016/s0960-894x(03)00621-8
44392734 65264 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 337 7 0 4 4.3 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2ccccc2C)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL182803 65264 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 337 7 0 4 4.3 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2ccccc2C)c1C 10.1016/j.bmcl.2004.05.072
44392787 131791 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 383 9 0 6 4.0 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2ccc(OC)cc2OC)c1C 10.1016/j.bmcl.2004.05.072
CHEMBL369333 131791 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 383 9 0 6 4.0 CCCN(CC1CC1)c1nc(C)nc(C(=O)c2ccc(OC)cc2OC)c1C 10.1016/j.bmcl.2004.05.072
44443645 154759 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 434 9 2 7 4.2 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCO 10.1016/j.bmcl.2007.09.008
CHEMBL400082 154759 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cellsDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in IMR32 cells
ChEMBL 434 9 2 7 4.2 CCc1nc(Oc2cc(C)ccn2)c(CC)nc1N[C@@H]1c2ccccc2C[C@@H]1OCCO 10.1016/j.bmcl.2007.09.008
10295681 18867 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 419 7 1 4 6.4 CCCN(CCC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
CHEMBL128201 18867 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.Binding affinity by displacement of [125I]Tyr-o-CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cell.
ChEMBL 419 7 1 4 6.4 CCCN(CCC)C(=O)c1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C 10.1016/j.bmcl.2003.08.055
10622505 59061 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 8 0 7 4.3 CCCCN(CC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1S(C)(=O)=O 10.1021/jm980224g
CHEMBL169521 59061 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 429 8 0 7 4.3 CCCCN(CC)c1cc(C)nc2c1nnn2-c1ccc(C(C)C)cc1S(C)(=O)=O 10.1021/jm980224g
11453549 70569 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 442 10 0 6 5.9 CCCC(c1ccccc1)N(CCC)c1nc(-c2cc(OC)c(OC)cc2Cl)n(C)n1 10.1021/jm049339c
CHEMBL194877 70569 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 442 10 0 6 5.9 CCCC(c1ccccc1)N(CCC)c1nc(-c2cc(OC)c(OC)cc2Cl)n(C)n1 10.1021/jm049339c
44266513 4222 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 485 6 0 3 8.2 CCN(c1nc(C)cc(-c2cccc(-c3ccccc3)c2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
CHEMBL10032 4222 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 485 6 0 3 8.2 CCN(c1nc(C)cc(-c2cccc(-c3ccccc3)c2)n1)c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00132-8
11291132 65217 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 352 6 1 6 3.9 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL182595 65217 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 352 6 1 6 3.9 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N)cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
11291132 65217 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 352 6 1 6 3.9 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL182595 65217 0 None - 1 Human 7.1 pKi = 7.1 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 352 6 1 6 3.9 CCCN(CCC)c1cc(C)nc2c(-c3ncc(N)cc3C)c(C)nn12 10.1021/jm040058e
44407873 98236 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 414 5 1 4 5.7 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)Cc2ccc(Cl)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
CHEMBL274388 98236 0 None - 1 Rat 6.1 pKi = 6.1 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenatesDisplacement of [125I]Tyr-o-CRF from CRF1 receptor in rat frontal cortex homogenates
ChEMBL 414 5 1 4 5.7 Cc1cc(C)c(Nc2nc(C)ccc2S(=O)(=O)Cc2ccc(Cl)cc2)c(C)c1 10.1016/j.bmcl.2005.10.097
44306205 203055 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 395 10 0 5 5.1 CCCN(c1ncc(CC)c(-c2ccc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
CHEMBL63585 203055 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cellsBinding affinity towards human Corticotropin releasing factor receptor 1 by the displacement of [125I]CRF from CHO cells
ChEMBL 395 10 0 5 5.1 CCCN(c1ncc(CC)c(-c2ccc(OC)cc2OC)n1)C(C1CC1)C1CC1 10.1016/j.bmcl.2004.02.053
10958953 203551 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 346 5 1 5 3.7 CC(=O)/C(=N\Nc1ccccc1[N+](=O)[O-])N(C)c1cccc(Cl)c1 10.1021/jm025512y
CHEMBL66602 203551 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity against human Corticotropin releasing factor receptor 1Binding affinity against human Corticotropin releasing factor receptor 1
ChEMBL 346 5 1 5 3.7 CC(=O)/C(=N\Nc1ccccc1[N+](=O)[O-])N(C)c1cccc(Cl)c1 10.1021/jm025512y
44392724 123112 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 357 6 0 5 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cn3)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL361099 123112 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 357 6 0 5 4.7 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cn3)c(C)nn12 10.1016/j.bmcl.2004.05.056
11348744 127177 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 352 5 0 6 3.1 CCCCN1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL365745 127177 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 352 5 0 6 3.1 CCCCN1CCn2c(=O)n(-c3ccc(OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
44385524 166114 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 445 7 1 6 5.3 CCCCN(CC)c1nc(C)nc2c1nc(O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
CHEMBL426026 166114 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligandBinding affinity for transfected human Corticotropin releasing factor receptor expressed in HEK 293E cells using [125I]TYR-oCRH as the displaced radioligand
ChEMBL 445 7 1 6 5.3 CCCCN(CC)c1nc(C)nc2c1nc(O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00108-0
10717634 4492 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 432 9 0 4 6.5 CCCN(CCC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL10203 4492 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 432 9 0 4 6.5 CCCN(CCC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10026532 97282 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 444 9 0 4 6.5 CCCN(CC1CC1)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL268993 97282 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 444 9 0 4 6.5 CCCN(CC1CC1)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
10576982 120452 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 488 6 0 4 5.2 CCN(CC)c1cc(C)nc(N(CC)c2ccc(I)cc2Br)n1 10.1021/jm980222w
CHEMBL353973 120452 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 488 6 0 4 5.2 CCN(CC)c1cc(C)nc(N(CC)c2ccc(I)cc2Br)n1 10.1021/jm980222w
44341714 10109 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 382 7 0 3 6.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)c(OC)ccc12 10.1016/s0960-894x(03)00684-x
CHEMBL115566 10109 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligandBinding affinity towards cloned human Corticotropin releasing factor receptor 1 expressed in CHO cells using [125I]o-CRF as the radioligand
ChEMBL 382 7 0 3 6.5 CCCN(CCC)c1cc(C)nc2c(-c3ccc(Cl)cc3)c(OC)ccc12 10.1016/s0960-894x(03)00684-x
10138067 6637 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 6 0 4 6.0 CCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC1CC1 10.1016/j.bmcl.2010.04.094
CHEMBL1083319 6637 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 438 6 0 4 6.0 CCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC1CC1 10.1016/j.bmcl.2010.04.094
10717634 4492 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 432 9 0 4 6.5 CCCN(CCC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1016/s0960-894x(99)00132-8
CHEMBL10203 4492 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 432 9 0 4 6.5 CCCN(CCC)c1cc(C)nc(N(CC)c2ccc(C(C)C)cc2Br)n1 10.1016/s0960-894x(99)00132-8
44446729 94867 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 390 8 0 3 6.7 CCCN(CCC)c1c(CC)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253913 94867 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 390 8 0 3 6.7 CCCN(CCC)c1c(CC)nc(-c2c(C)cc(C)cc2OC)c2ccccc12 10.1016/j.bmcl.2007.12.050
24971237 188049 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 380 8 0 6 4.7 CCC(CC)Oc1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL497653 188049 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 380 8 0 6 4.7 CCC(CC)Oc1c(C)nc(-c2c(OC)cc(Cl)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
44587457 188166 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 396 9 0 6 5.0 CCC(CC)Oc1c(C)nc(-c2c(OC)cc(C(F)F)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL498667 188166 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 396 9 0 6 5.0 CCC(CC)Oc1c(C)nc(-c2c(OC)cc(C(F)F)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
11338351 78331 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 9 0 5 5.6 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL2094044 78331 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 9 0 5 5.6 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
CHEMBL2109792 78331 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 392 9 0 5 5.6 CCC[C@@H](c1ccccc1)N(CCC)c1nc(-c2ccc(OC)cc2C)n(C)n1 10.1021/jm049339c
9886113 9223 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 378 7 0 4 5.2 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
CHEMBL110609 9223 0 None - 1 Human 8.1 pKi = 8.1 Binding
Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.Inhibition of [125I]o-CRF binding to human Corticotropin releasing factor receptor 1 expressed in CHO cells.
ChEMBL 378 7 0 4 5.2 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(C)n1)C(C1CC1)C1CC1 10.1016/s0960-894x(01)00657-6
11773483 65573 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc([N+](=O)[O-])cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
CHEMBL183148 65573 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc([N+](=O)[O-])cc3C)c(C)nn12 10.1016/j.bmcl.2004.05.056
20780255 7389 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 452 7 0 4 6.3 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC1CC1 10.1016/j.bmcl.2010.04.094
CHEMBL1086468 7389 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 452 7 0 4 6.3 CCCN(Cc1c(C(F)(F)F)nc2n(-c3c(C)cc(C)cc3C)c(Cl)cn12)CC1CC1 10.1016/j.bmcl.2010.04.094
15490818 4942 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 461 6 0 5 6.0 CCN(c1nc(C)cc(-c2ccccc2Cl)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
CHEMBL10473 4942 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 461 6 0 5 6.0 CCN(c1nc(C)cc(-c2ccccc2Cl)n1)c1c(Br)cc(OC)cc1OC 10.1016/s0960-894x(99)00132-8
11773483 65573 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc([N+](=O)[O-])cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL183148 65573 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 382 7 0 7 4.3 CCCN(CCC)c1cc(C)nc2c(-c3ncc([N+](=O)[O-])cc3C)c(C)nn12 10.1021/jm040058e
9929418 161768 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 372 4 0 6 5.3 CCN(CC)c1nc(C)nc2c1sc(=S)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
CHEMBL413968 161768 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 372 4 0 6 5.3 CCN(CC)c1nc(C)nc2c1sc(=S)n2-c1c(C)cc(C)cc1C 10.1016/s0960-894x(99)00159-6
10836468 120265 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 431 7 0 6 4.5 CCN(CCOC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL352438 120265 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 431 7 0 6 4.5 CCN(CCOC)c1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
9886113 9223 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 378 7 0 4 5.2 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(C)n1)C(C1CC1)C1CC1 10.1021/jm049339c
CHEMBL110609 9223 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 378 7 0 4 5.2 CCCN(c1nc(-c2ccc(Cl)cc2Cl)n(C)n1)C(C1CC1)C1CC1 10.1021/jm049339c
9803011 98852 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 434 5 0 6 4.9 CCN(CC)c1nc(C)nc2c1sc(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
CHEMBL278895 98852 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRHBinding affinity against human Corticotropin releasing factor receptor 1 expressed in HEK 293E cells using [125I]TYR-oCRH
ChEMBL 434 5 0 6 4.9 CCN(CC)c1nc(C)nc2c1sc(=O)n2-c1ccc(C(C)C)cc1Br 10.1016/s0960-894x(99)00159-6
9910700 59045 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 1 7 4.2 CCC(COC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169416 59045 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 1 7 4.2 CCC(COC)Nc1nc(C)nc2c1nnn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
9803011 98852 0 None - 1 Human 8.0 pKi = 8.0 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptorsCompound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors
ChEMBL 434 5 0 6 4.9 CCN(CC)c1nc(C)nc2c1sc(=O)n2-c1ccc(C(C)C)cc1Br 10.1021/jm990590f
CHEMBL278895 98852 0 None - 1 Human 8.0 pKi = 8.0 Binding
Compound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptorsCompound was tested for the binding affinity to human corticotropin releasing factor 1 (hCRF1) receptors
ChEMBL 434 5 0 6 4.9 CCN(CC)c1nc(C)nc2c1sc(=O)n2-c1ccc(C(C)C)cc1Br 10.1021/jm990590f
18691325 4191 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 508 6 0 5 6.5 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1c(Br)cc(N(C)C)cc1OC 10.1016/s0960-894x(99)00132-8
CHEMBL10015 4191 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cellsDisplacement of [125I]-TYR-ovine CRH from cloned human corticotropin releasing factor receptor 1 expressed in 293 EBNA cells
ChEMBL 508 6 0 5 6.5 CCN(c1nc(C)cc(-c2ccccc2C(F)(F)F)n1)c1c(Br)cc(N(C)C)cc1OC 10.1016/s0960-894x(99)00132-8
11326060 67017 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 6 1 6 4.4 CCC(CC)Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
CHEMBL186992 67017 0 None - 1 Human 8.0 pKi = 8.0 Binding
Inhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptorInhibition of [125I]o-CRF binding to CHO cells expressing human CRF1 receptor
ChEMBL 366 6 1 6 4.4 CCC(CC)Nc1cc(C)nc2c(-c3cnc(N(C)C)cc3C)c(C)nn12 10.1021/jm040058e
10646423 59361 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 0 6 4.8 CCC(COC)Oc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL170788 59361 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 432 7 0 6 4.8 CCC(COC)Oc1nc(C)nc2c1ncn2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341805 110518 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 406 6 0 5 5.1 COCCN(c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12)C(C)C 10.1016/s0960-894x(03)00622-x
CHEMBL325051 110518 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 406 6 0 5 5.1 COCCN(c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12)C(C)C 10.1016/s0960-894x(03)00622-x
10528542 59089 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 474 9 0 6 5.0 COCCN(CCOC)c1cc(C)nc2c1nc(C)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
CHEMBL169641 59089 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cellsBinding affinity to recombinant human Corticotropin releasing factor receptor 1 (hCRF1) expressed in 293EBNA cells
ChEMBL 474 9 0 6 5.0 COCCN(CCOC)c1cc(C)nc2c1nc(C)n2-c1ccc(C(C)C)cc1Br 10.1021/jm980224g
44341835 9495 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 420 8 0 5 5.5 CCCN(CCCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
CHEMBL112045 9495 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cellsBinding affinity towards Corticotropin releasing factor receptor 1 was measured through displacement of [125I]sauvagine expressed in HEK293 cells
ChEMBL 420 8 0 5 5.5 CCCN(CCCOC)c1cc(C)nc2c(-c3ccc(Cl)cc3Cl)nn(C)c12 10.1016/s0960-894x(03)00622-x
9822241 64009 8 None -9 2 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation counting
ChEMBL 399 8 1 6 5.0 CCC(CC)Nc1nc(C)c(-c2ccc(OC(F)(F)F)cc2OC)nc1OC 10.1021/jm200365y
CHEMBL1807053 64009 8 None -9 2 Rat 8.0 pKi = 8.0 Binding
Displacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation countingDisplacement of [125I]-sauvagine from rat CRF-1 receptor expressed in rat cortical membrane after 2 hrs by scintillation counting
ChEMBL 399 8 1 6 5.0 CCC(CC)Nc1nc(C)c(-c2ccc(OC(F)(F)F)cc2OC)nc1OC 10.1021/jm200365y
11546255 188117 0 None 12022 2 Human 8.0 pKi = 8 Binding
Binding affinity to human recombinant CRF1 in HEK cell line assessed as inhibition constant incubated for 2 hrs by MicroBeta scintillation counter methodBinding affinity to human recombinant CRF1 in HEK cell line assessed as inhibition constant incubated for 2 hrs by MicroBeta scintillation counter method
ChEMBL 419 5 0 7 4.9 CCC(CC)c1cc(C)nn2c(-c3sc(N4CCOCC4)nc3Cl)c(C)nc12 10.1016/j.ejmech.2021.113867
CHEMBL498311 188117 0 None 12022 2 Human 8.0 pKi = 8 Binding
Binding affinity to human recombinant CRF1 in HEK cell line assessed as inhibition constant incubated for 2 hrs by MicroBeta scintillation counter methodBinding affinity to human recombinant CRF1 in HEK cell line assessed as inhibition constant incubated for 2 hrs by MicroBeta scintillation counter method
ChEMBL 419 5 0 7 4.9 CCC(CC)c1cc(C)nn2c(-c3sc(N4CCOCC4)nc3Cl)c(C)nc12 10.1016/j.ejmech.2021.113867
9950645 105243 0 None - 1 Human 7.1 pKi = 7.1 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 357 7 0 5 4.0 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(C)c1=O 10.1016/s0960-894x(03)00483-9
CHEMBL311520 105243 0 None - 1 Human 7.1 pKi = 7.1 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 357 7 0 5 4.0 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)n(C)c1=O 10.1016/s0960-894x(03)00483-9
10686834 120459 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 315 5 0 5 4.2 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)=O)cc1SC 10.1021/jm980222w
CHEMBL354022 120459 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for human recombinant corticotropin releasing factor receptor 1Binding affinity for human recombinant corticotropin releasing factor receptor 1
ChEMBL 315 5 0 5 4.2 CCN(c1nc(C)cc(C)n1)c1ccc(C(C)=O)cc1SC 10.1021/jm980222w
44392742 123573 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 409 11 0 4 5.8 CCCN(CC1CC1)c1cc(C(OC)c2c(CC)cc(CC)cc2CC)nc(C)n1 10.1016/j.bmcl.2004.05.072
CHEMBL361831 123573 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity for recombinant human CRF1 receptorBinding affinity for recombinant human CRF1 receptor
ChEMBL 409 11 0 4 5.8 CCCN(CC1CC1)c1cc(C(OC)c2c(CC)cc(CC)cc2CC)nc(C)n1 10.1016/j.bmcl.2004.05.072
11440355 63009 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 378 8 0 5 5.0 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(C(C)C)C(C)C 10.1021/jm049339c
CHEMBL178702 63009 0 None - 1 Human 6.0 pKi = 6.0 Binding
Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells Inhibition of [125I][Tyr0]-sauvagine binding to human Corticotropin releasing factor receptor 1 expressed in mouse fibroblast Ltk- cells
ChEMBL 378 8 0 5 5.0 CCCN(c1nc(-c2ccc(Cl)cc2OC)n(C)n1)C(C(C)C)C(C)C 10.1021/jm049339c
11304752 67655 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 422 7 0 7 4.1 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(C(=O)OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
CHEMBL190661 67655 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cellsBinding affinity for corticotropin-releasing factor-1 expressed in leukocyte tyrosine kinase cells
ChEMBL 422 7 0 7 4.1 CCCC(CCC)N1CCn2c(=O)n(-c3ccc(C(=O)OC)cc3)c3nc(C)cc1c32 10.1021/jm050384+
21916077 7284 0 None - 1 Human 6.0 pKi = 6.0 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 442 3 0 5 5.3 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCSCC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
CHEMBL1086017 7284 0 None - 1 Human 6.0 pKi = 6.0 Binding
Displacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 minsDisplacement of [125I] Tyr-o-CRF from human CRF[125I]receptor expressed in human IMR-3[125I]cells after 100 mins
ChEMBL 442 3 0 5 5.3 Cc1cc(C)c(-n2c(Cl)cn3c(CN4CCSCC4)c(C(F)(F)F)nc23)c(C)c1 10.1016/j.bmcl.2010.04.094
44317760 205555 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 378 7 1 3 5.7 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2C)c(Cl)c1 10.1021/jm049974i
CHEMBL81117 205555 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human corticotropin releasing factor (h-CRF1) receptorBinding affinity towards human corticotropin releasing factor (h-CRF1) receptor
ChEMBL 378 7 1 3 5.7 Cc1ccc(NC(C(=O)CCc2ccncc2)c2ccccc2C)c(Cl)c1 10.1021/jm049974i
44305209 203431 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 424 6 0 4 6.6 CCCCN(CC)c1cc(C)nc2c(-c3c(Cl)cc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
CHEMBL65724 203431 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cellsDisplacement of [125I]0-CRF from human Corticotropin releasing factor receptor 1 expressed in CHO cells
ChEMBL 424 6 0 4 6.6 CCCCN(CC)c1cc(C)nc2c(-c3c(Cl)cc(Cl)cc3Cl)c(C)nn12 10.1016/s0960-894x(98)00372-2
20780175 166603 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 401 6 0 5 5.1 CCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
CHEMBL428048 166603 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP productionDisplacement of [125I]Tyr-o-CRF from CRF1 receptor expressed in IMR32 cells assessed as inhibition of CRF stimulated cAMP production
ChEMBL 401 6 0 5 5.1 CCN(Cc1c(C)nc2n(-c3c(C)cc(C)cc3C)c3ncccc3n12)CC1CC1 10.1016/j.bmcl.2007.01.008
135553002 205690 0 None - 1 Human 6.0 pKi = 6.0 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 343 7 1 5 4.4 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1O 10.1016/s0960-894x(03)00483-9
CHEMBL82265 205690 0 None - 1 Human 6.0 pKi = 6.0 Binding
Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.Affinity for Corticotropin releasing factor receptor 1 on IMR-32 (human neuroblastoma) cells by [125I]-sauvagine displacement.
ChEMBL 343 7 1 5 4.4 CCCN(CCC)c1c(C)nc(-c2c(C)cc(C)cc2OC)nc1O 10.1016/s0960-894x(03)00483-9
44397631 67146 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 460 7 0 4 6.2 CCCN(CC1CC1)C(=O)c1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ccc(F)cc3n12 10.1016/j.bmcl.2005.06.028
CHEMBL187577 67146 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity for human corticotropin releasing factor receptor 1Binding affinity for human corticotropin releasing factor receptor 1
ChEMBL 460 7 0 4 6.2 CCCN(CC1CC1)C(=O)c1c(CC)nc2n(-c3c(C)cc(C)cc3C)c3ccc(F)cc3n12 10.1016/j.bmcl.2005.06.028
11689443 64367 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 380 6 0 4 4.4 CCc1nc2n(c1C(=O)N(CC)CC1CC1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
CHEMBL181283 64367 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 380 6 0 4 4.4 CCc1nc2n(c1C(=O)N(CC)CC1CC1)CCN2c1c(C)cc(C)cc1C 10.1016/j.bmcl.2005.05.117
20780028 131372 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 414 7 0 4 5.1 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1Cl 10.1016/j.bmcl.2005.05.117
CHEMBL368879 131372 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cellsDisplacement of [125I]-Tyr-o- CRF from human corticotropin releasing factor receptor 1 expressed in IMR-32 cells
ChEMBL 414 7 0 4 5.1 CCCN(CC1CC1)C(=O)c1c(CC)nc2n1CCN2c1c(C)cc(C)cc1Cl 10.1016/j.bmcl.2005.05.117
44587377 172927 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 343 7 1 5 4.7 CCC(CC)Nc1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
CHEMBL451660 172927 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cellsDisplacement of [125I]sauvagine from human CRF1 receptor expressed in IMR32 cells
ChEMBL 343 7 1 5 4.7 CCC(CC)Nc1c(C)nc(-c2c(C)cc(C)cc2OC)nc1OC 10.1016/j.bmcl.2008.07.063
10616689 58737 1 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 333 3 0 3 4.7 Cc1cc(C)nc(N(C)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980223o
CHEMBL168568 58737 1 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity was determined against corticotropin releasing factor receptor 1Binding affinity was determined against corticotropin releasing factor receptor 1
ChEMBL 333 3 0 3 4.7 Cc1cc(C)nc(N(C)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980223o
10616689 58737 1 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 333 3 0 3 4.7 Cc1cc(C)nc(N(C)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
CHEMBL168568 58737 1 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity was measured on rat Corticotropin releasing factor receptor 1Binding affinity was measured on rat Corticotropin releasing factor receptor 1
ChEMBL 333 3 0 3 4.7 Cc1cc(C)nc(N(C)c2ccc(C(C)C)cc2Br)n1 10.1021/jm980222w
44446719 94778 0 None - 1 Human 6.0 pKi = 6.0 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 352 6 0 2 6.5 CCCN(CCC)c1c(C)nc(-c2ccc(Cl)cc2)c2ccccc12 10.1016/j.bmcl.2007.12.050
CHEMBL253286 94778 0 None - 1 Human 6.0 pKi = 6.0 Binding
Displacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cellsDisplacement of [125I]sauvagine from CRF1 receptor expressed in human IMR32 cells
ChEMBL 352 6 0 2 6.5 CCCN(CCC)c1c(C)nc(-c2ccc(Cl)cc2)c2ccccc12 10.1016/j.bmcl.2007.12.050
44389088 62974 0 None - 1 Human 5.0 pKi = 5.0 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 459 6 1 4 7.5 CC(C)N(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)C(C)C 10.1016/j.bmcl.2004.10.055
CHEMBL178523 62974 0 None - 1 Human 5.0 pKi = 5.0 Binding
Inhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cellsInhibition of [125I]Tyr-o-CRF binding to Corticotropin releasing factor receptor 1 expressed in IMR-32 human neuroblastoma cells
ChEMBL 459 6 1 4 7.5 CC(C)N(Cc1sc(Nc2c(Cl)cc(Cl)cc2Cl)nc1C(F)(F)F)C(C)C 10.1016/j.bmcl.2004.10.055
10379 3059 39 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes.Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes.
Guide to Pharmacology 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 28174066
9884366 3059 39 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes.Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes.
Guide to Pharmacology 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 28174066
CHEMBL482950 3059 39 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes.Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes.
Guide to Pharmacology 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 28174066
DB12572 3059 39 None - 1 Human 6.5 pIC50 = 6.5 Binding
Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes.Displacement of ovine [125-I]-CRF from human CRF1 receptor expressed in CHO cell membranes.
Guide to Pharmacology 340 5 1 7 3.3 CC[C@H](Nc1nc(C)nc2n1nc(c2c1ccc(nc1C)OC)C)C 28174066
10377 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
In vitro binding to rat cortex.In vitro binding to rat cortex.
Guide to Pharmacology 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18260619
9818802 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
In vitro binding to rat cortex.In vitro binding to rat cortex.
Guide to Pharmacology 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18260619
CHEMBL270738 1179 27 None 1 2 Rat 8.2 pIC50 = 8.2 Binding
In vitro binding to rat cortex.In vitro binding to rat cortex.
Guide to Pharmacology 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18260619
912 1167 0 None 1 4 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11123370
912 1167 0 None 1 4 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7477349
912 1167 0 None 1 4 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7692441
912 1167 0 None 1 4 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8612563
912 1167 0 None 1 4 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9326293
912 1167 0 None 1 4 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9851694
913 1168 0 None 44 2 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11123370
913 1168 0 None 44 2 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15450949
913 1168 0 None 44 2 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9326293
913 1168 0 None 44 2 Human 8.1 pKd = 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9851694
16133798 506 0 None -3 4 Human 8.3 pKd = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11123370
16133798 506 0 None -3 4 Human 8.3 pKd = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9851694
16133798 506 0 None -3 4 Human 8.3 pKd = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9918582
925 506 0 None -3 4 Human 8.3 pKd = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11123370
925 506 0 None -3 4 Human 8.3 pKd = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9851694
925 506 0 None -3 4 Human 8.3 pKd = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9918582
920 3949 0 None -1 3 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11123370
920 3949 0 None -1 3 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11416224
920 3949 0 None -1 3 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7477349
920 3949 0 None -1 3 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8612563
920 3949 0 None -1 3 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9918582
919 3950 0 None -1 4 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11123370
919 3950 0 None -1 4 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15450949
919 3950 0 None -1 4 Human 9.1 pKd = 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8612563
921 3953 0 None -8912 4 Human 5.4 pKd None 5.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15450949
CHEMBL429970 3953 0 None -8912 4 Human 5.4 pKd None 5.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15450949
155817385 360 0 None -31 3 Human 7.6 pKd None 7.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9918582
923 360 0 None -31 3 Human 7.6 pKd None 7.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9918582
918 3488 0 None -3 4 Human 8.0 pKd None 8.0 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11123370
918 3488 0 None -3 4 Human 8.0 pKd None 8.0 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15450949
918 3488 0 None -3 4 Human 8.0 pKd None 8.0 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7477349
918 3488 0 None -3 4 Human 8.0 pKd None 8.0 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8612563
918 3488 0 None -3 4 Human 8.0 pKd None 8.0 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9326293
918 3488 0 None -3 4 Human 8.0 pKd None 8.0 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9918582
922 3957 0 None 1 3 Human 8.6 pKd None 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 11123370
922 3957 0 None 1 3 Human 8.6 pKd None 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7477349
177990 426 23 125I-Sauvagine -1 2 Human 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
3489 426 23 125I-Sauvagine -1 2 Human 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
CHEMBL296641 426 23 125I-Sauvagine -1 2 Human 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
177990 426 23 3H-NBI 35965 + GTP GammaS -1 2 Human 9.2 pKi = 9.2 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
3489 426 23 3H-NBI 35965 + GTP GammaS -1 2 Human 9.2 pKi = 9.2 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
CHEMBL296641 426 23 3H-NBI 35965 + GTP GammaS -1 2 Human 9.2 pKi = 9.2 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
177990 426 23 125I-Sauvigine + GTP GammaS -1 2 Human 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
3489 426 23 125I-Sauvigine + GTP GammaS -1 2 Human 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
CHEMBL296641 426 23 125I-Sauvigine + GTP GammaS -1 2 Human 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
177990 426 23 125I-Sauvagine -1 2 Human 8.5 pKi = 8.5 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
3489 426 23 125I-Sauvagine -1 2 Human 8.5 pKi = 8.5 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
CHEMBL296641 426 23 125I-Sauvagine -1 2 Human 8.5 pKi = 8.5 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
177990 426 23 125I-Astressin + GTP GammaS -1 2 Human 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
3489 426 23 125I-Astressin + GTP GammaS -1 2 Human 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
CHEMBL296641 426 23 125I-Astressin + GTP GammaS -1 2 Human 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC None
10377 1179 27 None -1 2 Human 8.1 pKi = 8.1 Binding
Antagonism of CRF-stimulated adenylate cyclase activity by the CRF1 receptor endogenously expressed in human IMR32 cells.Antagonism of CRF-stimulated adenylate cyclase activity by the CRF1 receptor endogenously expressed in human IMR32 cells.
Guide to Pharmacology 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18260619
9818802 1179 27 None -1 2 Human 8.1 pKi = 8.1 Binding
Antagonism of CRF-stimulated adenylate cyclase activity by the CRF1 receptor endogenously expressed in human IMR32 cells.Antagonism of CRF-stimulated adenylate cyclase activity by the CRF1 receptor endogenously expressed in human IMR32 cells.
Guide to Pharmacology 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18260619
CHEMBL270738 1179 27 None -1 2 Human 8.1 pKi = 8.1 Binding
Antagonism of CRF-stimulated adenylate cyclase activity by the CRF1 receptor endogenously expressed in human IMR32 cells.Antagonism of CRF-stimulated adenylate cyclase activity by the CRF1 receptor endogenously expressed in human IMR32 cells.
Guide to Pharmacology 327 6 0 3 6.0 CCC(Oc1cc(C)nc(c1C)Oc1c(C)cc(cc1C)C)CC 18260619
10378 3985 37 None - 1 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 21074436
11596613 3985 37 None - 1 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 21074436
CHEMBL1287935 3985 37 None - 1 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 21074436
DB12512 3985 37 None - 1 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 406 6 1 8 4.6 COc1ccc(c(c1)C)c1c(C)nn2c1nc(C)cc2N[C@H](c1onc(n1)C)CC 21074436
10375 2739 18 None - 1 Human 8.3 pKi = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 16078829
9888194 2739 18 None - 1 Human 8.3 pKi = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 16078829
CHEMBL188907 2739 18 None - 1 Human 8.3 pKi = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 416 6 0 4 6.5 CCCC(N1CCn2c3c1cc(C)nc3c(n2)c1ccc(cc1Cl)Cl)CCC 16078829
11025 2740 7 None -1 2 Rat 8.4 pKi = 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 12957366
11713007 2740 7 None -1 2 Rat 8.4 pKi = 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 12957366
CHEMBL380800 2740 7 None -1 2 Rat 8.4 pKi = 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 400 4 0 4 5.7 CC[C@H]1Cn2nc(c3c2c(N1CC1CC1)cc(n3)C)c1ccc(cc1Cl)Cl 12957366
177990 426 23 None -1 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 8940412
3489 426 23 None -1 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 8940412
CHEMBL296641 426 23 None -1 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 378 6 0 4 5.9 CCCCN(c1nc(C)nc2c1c(C)c(n2c1c(C)cc(cc1C)C)C)CC 8940412
3499 1448 28 None - 1 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10669572
9909468 1448 28 None - 1 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10669572
CHEMBL44698 1448 28 None - 1 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 409 7 1 7 3.8 COCC(Nc1nc(C)nc2n1nc(c2c1ccc(cc1Cl)Cl)C)COC 10669572
176157 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 8893829
3512 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 8893829
CHEMBL45281 2738 28 None 9 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 432 7 1 4 6.8 CCCN(c1nc(C)nc(c1Cl)Nc1c(Cl)cc(cc1Cl)Cl)CC1CC1 8893829
3520 3267 54 None 1 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10867111
9821250 3267 54 None 1 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10867111
CHEMBL309138 3267 54 None 1 2 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 380 7 0 6 4.4 CCCN(c1cc(C)nc2n1nc(c2c1cnc(cc1C)N(C)C)C)CCC 10867111
16133798 506 0 None -3 4 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 24269930
925 506 0 None -3 4 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 24269930
3533 1206 24 None - 1 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 11907190
5282340 1206 24 None - 1 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 11907190
CHEMBL291657 1206 24 None - 1 Human 8.7 pKi = 8.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 482 8 0 4 7.5 C#CCN([C@H](c1ccc(c(c1)F)C)CC1CC1)c1sc(c(n1)c1cc(C)c(cc1Cl)OC)C 11907190