BMY-7378
SMILES | COc1ccccc1N1CCN(CC1)CCN1C(=O)CC2(CC1=O)CCCC2 |
InChIKey | AYYCFGDXLUPJAQ-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 5 |
Hydrogen bond donors | 0 |
Rotatable bonds | 5 |
Molecular weight (Da) | 385.2 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Database connections
Ligand site mutations | α1A |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
α1A | ADA1A | Human | Adrenoceptors | A | pKi | 6.6 | 6.8 | 7.0 | Guide to Pharmacology |
α1D | ADA1D | Human | Adrenoceptors | A | pKi | 8.6 | 8.85 | 9.1 | Guide to Pharmacology |
α1D | ADA1D | Rat | Adrenoceptors | A | pKi | 9.0 | 9.0 | 9.0 | Guide to Pharmacology |
α1A | ADA1A | Rat | Adrenoceptors | A | pKi | 7.0 | 7.0 | 7.0 | Guide to Pharmacology |
α1A | ADA1A | Bovine | Adrenoceptors | A | pKi | 7.37 | 7.37 | 7.37 | ChEMBL |
α1D | ADA1D | Rat | Adrenoceptors | A | pKd | 8.22 | 8.36 | 8.52 | ChEMBL |
α1D | ADA1D | Rat | Adrenoceptors | A | pKi | 8.07 | 8.57 | 9.02 | ChEMBL |
α1B | ADA1B | Rat | Adrenoceptors | A | pKd | 7.37 | 7.5 | 7.55 | ChEMBL |
α1B | ADA1B | Rat | Adrenoceptors | A | pKi | 6.48 | 6.48 | 6.48 | ChEMBL |
α1B | ADA1B | Human | Adrenoceptors | A | pKi | 6.15 | 6.46 | 7.3 | ChEMBL |
α1A | ADA1A | Rat | Adrenoceptors | A | pKi | 6.21 | 6.49 | 6.95 | ChEMBL |
α1A | ADA1A | Rat | Adrenoceptors | A | pKd | 5.98 | 6.76 | 7.01 | ChEMBL |
α1D | ADA1D | Human | Adrenoceptors | A | pKi | 8.2 | 8.82 | 9.11 | ChEMBL |
D2 | DRD2 | Rat | Dopamine | A | pKi | 7.31 | 7.43 | 7.76 | ChEMBL |
α1A | ADA1A | Human | Adrenoceptors | A | pKi | 6.36 | 6.54 | 7.37 | ChEMBL |
α1A | ADA1A | Human | Adrenoceptors | A | pKd | 6.42 | 6.42 | 6.42 | ChEMBL |
5-HT1A | 5HT1A | Rat | 5-Hydroxytryptamine | A | pKi | 7.1 | 8.13 | 8.71 | ChEMBL |
5-HT1A | 5HT1A | Human | 5-Hydroxytryptamine | A | pKi | 8.76 | 9.09 | 9.43 | ChEMBL |
α1B | ADA1B | Human | Adrenoceptors | A | pKi | 6.2 | 6.85 | 7.5 | Guide to Pharmacology |
D2 | DRD2 | Human | Dopamine | A | pKi | 7.85 | 7.85 | 7.85 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
5-HT1A | 5HT1A | Human | 5-Hydroxytryptamine | A | pIC50 | 6.8 | 7.4 | 8.0 | Guide to Pharmacology |
5-HT1A | 5HT1A | Rat | 5-Hydroxytryptamine | A | pIC50 | 8.62 | 8.62 | 8.62 | ChEMBL |
M1 | ACM1 | Rat | Acetylcholine (muscarinic) | A | Potency | 4.85 | 4.88 | 4.9 | ChEMBL |