CHEMBL4277264
| SMILES | Cc1cc(Oc2nccc3occc23)ccc1-c1c(C)ncc2nccn12 |
| InChIKey | HWAIAGZSWHOLLK-UHFFFAOYSA-N |
Chemical properties
| Hydrogen bond acceptors | 6 |
| Hydrogen bond donors | 0 |
| Rotatable bonds | 3 |
| Molecular weight (Da) | 356.1 |
Drug properties
| Molecular type | Small molecule |
| Physiological/Surrogate | Surrogate |
| Approved drug | No |
Database connections
| Structure pdb | 8JXS |
Bioactivities
| Receptor | Activity | Source | |||||||
|---|---|---|---|---|---|---|---|---|---|
| GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
| 5-HT1E | 5HT1E | Human | 5-Hydroxytryptamine | A | pKi | 5.01 | 5.01 | 5.01 | ChEMBL |
| D5 | DRD5 | Human | Dopamine | A | pKi | 7.42 | 7.87 | 8.32 | ChEMBL |
| 5-HT4 | 5HT4R | Human | 5-Hydroxytryptamine | A | pKi | 5.04 | 5.04 | 5.04 | ChEMBL |
| 5-HT1B | 5HT1B | Human | 5-Hydroxytryptamine | A | pKi | 5.03 | 5.03 | 5.03 | ChEMBL |
| 5-HT1D | 5HT1D | Human | 5-Hydroxytryptamine | A | pKi | 5.03 | 5.03 | 5.03 | ChEMBL |
| α1B | ADA1B | Human | Adrenoceptors | A | pKi | 5.04 | 5.04 | 5.04 | ChEMBL |
| H2 | HRH2 | Human | Histamine | A | pKi | 5.1 | 5.1 | 5.1 | ChEMBL |
| β1 | ADRB1 | Human | Adrenoceptors | A | pKi | 5.12 | 5.12 | 5.12 | ChEMBL |
| D4 | DRD4 | Human | Dopamine | A | pKi | 5.35 | 5.35 | 5.35 | ChEMBL |
| α1A | ADA1A | Human | Adrenoceptors | A | pKi | 5.47 | 5.47 | 5.47 | ChEMBL |
| α2A | ADA2A | Human | Adrenoceptors | A | pKi | 5.47 | 5.47 | 5.47 | ChEMBL |
| D1 | DRD1 | Human | Dopamine | A | pKi | 6.96 | 7.65 | 8.05 | ChEMBL |
| 5-HT2B | 5HT2B | Human | 5-Hydroxytryptamine | A | pKi | 5.39 | 5.39 | 5.39 | ChEMBL |
| M2 | ACM2 | Human | Acetylcholine (muscarinic) | A | pKi | 5.11 | 5.11 | 5.11 | ChEMBL |
| β2 | ADRB2 | Human | Adrenoceptors | A | pKi | 5.03 | 5.03 | 5.03 | ChEMBL |
| M1 | ACM1 | Human | Acetylcholine (muscarinic) | A | pKi | 5.06 | 5.06 | 5.06 | ChEMBL |
| D3 | DRD3 | Human | Dopamine | A | pKi | 5.1 | 5.1 | 5.1 | ChEMBL |
| 5-HT1A | 5HT1A | Human | 5-Hydroxytryptamine | A | pKi | 5.92 | 5.92 | 5.92 | ChEMBL |
| κ | OPRK | Human | Opioid | A | pKi | 5.51 | 5.51 | 5.51 | ChEMBL |
| μ | OPRM | Human | Opioid | A | pKi | 5.09 | 5.09 | 5.09 | ChEMBL |
| 5-HT2A | 5HT2A | Human | 5-Hydroxytryptamine | A | pKi | 5.31 | 5.31 | 5.31 | ChEMBL |
| 5-HT6 | 5HT6R | Human | 5-Hydroxytryptamine | A | pKi | 5.09 | 5.09 | 5.09 | ChEMBL |
| 5-HT7 | 5HT7R | Human | 5-Hydroxytryptamine | A | pKi | 5.11 | 5.11 | 5.11 | ChEMBL |
| D2 | DRD2 | Human | Dopamine | A | pKi | 5.08 | 5.08 | 5.08 | ChEMBL |
| Receptor | Activity | Source | |||||||
|---|---|---|---|---|---|---|---|---|---|
| GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
| H1 | HRH1 | Human | Histamine | A | pIC50 | 5.34 | 5.34 | 5.34 | ChEMBL |
| D1 | DRD1 | Human | Dopamine | A | pEC50 | 6.5 | 7.66 | 9.61 | ChEMBL |
| M1 | ACM1 | Human | Acetylcholine (muscarinic) | A | pIC50 | 5.31 | 5.31 | 5.31 | ChEMBL |
| CB1 | CNR1 | Human | Cannabinoid | A | pIC50 | 5.68 | 5.68 | 5.68 | ChEMBL |