BP 897
SMILES | COc1ccccc1N1CCN(CC1)CCCCNC(=O)c1ccc2c(c1)cccc2 |
InChIKey | MNHDKMDLOJSCGN-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 4 |
Hydrogen bond donors | 1 |
Rotatable bonds | 8 |
Molecular weight (Da) | 417.2 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Database connections
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
D3 | DRD3 | Human | Dopamine | A | pKi | 9.0 | 9.0 | 9.0 | Guide to Pharmacology |
D5 | DRD5 | Rat | Dopamine | A | pKi | 6.2 | 6.2 | 6.2 | ChEMBL |
D4 | DRD4 | Rat | Dopamine | A | pKi | 6.79 | 6.79 | 6.79 | ChEMBL |
D3 | DRD3 | Rat | Dopamine | A | pKi | 7.7 | 8.76 | 9.04 | ChEMBL |
D1 | DRD1 | Rat | Dopamine | A | pKi | 5.52 | 5.52 | 5.52 | ChEMBL |
α1A | ADA1A | Rat | Adrenoceptors | A | pKi | 7.22 | 7.22 | 7.22 | ChEMBL |
D2 | DRD2 | Rat | Dopamine | A | pKi | 6.33 | 6.77 | 7.21 | ChEMBL |
D4 | DRD4 | Human | Dopamine | A | pKi | 6.2 | 7.04 | 7.41 | ChEMBL |
α2A | ADA2A | Human | Adrenoceptors | A | pKi | 8.56 | 8.56 | 8.56 | ChEMBL |
D3 | DRD3 | Human | Dopamine | A | pKi | 8.34 | 8.92 | 9.52 | ChEMBL |
D3 | DRD3 | Human | Dopamine | A | pKd | 7.8 | 7.8 | 7.8 | ChEMBL |
5-HT1A | 5HT1A | Human | 5-Hydroxytryptamine | A | pKi | 6.76 | 7.01 | 7.09 | ChEMBL |
D2 | DRD2 | Human | Dopamine | A | pKi | 6.61 | 6.91 | 7.47 | ChEMBL |
D3 | DRD3 | Human | Dopamine | A | pKi | 8.85 | 8.85 | 8.85 | PDSP Ki database |
5-HT2B | 5HT2B | Human | 5-Hydroxytryptamine | A | pKi | 7.48 | 7.48 | 7.48 | ChEMBL |
5-HT2C | 5HT2C | Human | 5-Hydroxytryptamine | A | pKi | 6.66 | 6.66 | 6.66 | ChEMBL |
α1A | ADA1A | Human | Adrenoceptors | A | pKi | 8.04 | 8.04 | 8.04 | ChEMBL |
D1 | DRD1 | Human | Dopamine | A | pKi | 5.95 | 6.06 | 6.12 | ChEMBL |
D5 | DRD5 | Human | Dopamine | A | pKi | 5.91 | 5.91 | 5.91 | ChEMBL |
5-HT1A | 5HT1A | Rat | 5-Hydroxytryptamine | A | pKi | 7.08 | 7.08 | 7.08 | ChEMBL |
D1 | DRD1 | Pig | Dopamine | A | pKi | 6.12 | 6.12 | 6.12 | ChEMBL |
α2A | ADA2A | Rat | Adrenoceptors | A | pKi | 7.08 | 7.08 | 7.08 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
D3 | DRD3 | Rat | Dopamine | A | pIC50 | 9.14 | 9.27 | 9.39 | ChEMBL |
D2 | DRD2 | Rat | Dopamine | A | pIC50 | 7.55 | 7.58 | 7.62 | ChEMBL |
D4 | DRD4 | Human | Dopamine | A | pEC50 | 7.31 | 7.31 | 7.31 | ChEMBL |
D3 | DRD3 | Human | Dopamine | A | pEC50 | 8.52 | 8.64 | 8.74 | ChEMBL |
D3 | DRD3 | Human | Dopamine | A | pIC50 | 7.25 | 8.1 | 8.74 | ChEMBL |
TSH | TSHR | Human | Glycoprotein hormone | A | Potency | 4.8 | 4.8 | 4.8 | ChEMBL |
D3 | DRD3 | Green monkey | Dopamine | A | pEC50 | 8.52 | 8.52 | 8.52 | ChEMBL |
M1 | ACM1 | Rat | Acetylcholine (muscarinic) | A | Potency | 4.7 | 4.78 | 4.85 | ChEMBL |