CHEMBL1161318


SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@@H]1CC(=O)NCCCC[C@@H](C(N)=O)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)C2(CCCCC2)NC1=O
InChIKey FDLHDUZIGJCBAK-WRLVAQMBSA-N

Chemical properties

Hydrogen bond acceptors None
Hydrogen bond donors None
Rotatable bonds None
Molecular weight (Da)

Drug properties

Molecular type Protein
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC3 MC3R Human Melanocortin A pKd 6.5 6.5 6.5 ChEMBL
MC4 MC4R Human Melanocortin A pKd 8.4 8.4 8.4 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC5 MC5R Human Melanocortin A pIC50 8.34 8.34 8.34 ChEMBL
MC5 MC5R Human Melanocortin A pEC50 8.0 8.0 8.0 ChEMBL
MC3 MC3R Human Melanocortin A pIC50 7.39 7.39 7.39 ChEMBL
MC4 MC4R Human Melanocortin A pIC50 9.32 9.32 9.32 ChEMBL