AC-42
SMILES | CCCCC1CCN(CC1)CCCC(=O)c1ccccc1C |
InChIKey | ANTKBACNWQHQJE-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 2 |
Hydrogen bond donors | 0 |
Rotatable bonds | 8 |
Molecular weight (Da) | 301.2 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
M1 | ACM1 | Human | Acetylcholine (muscarinic) | A | pKi | 6.2 | 6.2 | 6.2 | Guide to Pharmacology |
5-HT1A | 5HT1A | Human | 5-Hydroxytryptamine | A | pKi | 6.55 | 6.55 | 6.55 | ChEMBL |
M1 | ACM1 | Human | Acetylcholine (muscarinic) | A | pKi | 5.76 | 5.9 | 6.05 | ChEMBL |
M2 | ACM2 | Human | Acetylcholine (muscarinic) | A | pKi | 6.01 | 6.01 | 6.01 | ChEMBL |
M3 | ACM3 | Human | Acetylcholine (muscarinic) | A | pKi | 5.55 | 5.55 | 5.55 | ChEMBL |
M4 | ACM4 | Human | Acetylcholine (muscarinic) | A | pKi | 5.85 | 5.85 | 5.85 | ChEMBL |
M5 | ACM5 | Human | Acetylcholine (muscarinic) | A | pKi | 5.35 | 5.35 | 5.35 | ChEMBL |
α1A | ADA1A | Human | Adrenoceptors | A | pKi | 7.75 | 7.75 | 7.75 | ChEMBL |
α1B | ADA1B | Human | Adrenoceptors | A | pKi | 7.19 | 7.19 | 7.19 | ChEMBL |
α1D | ADA1D | Human | Adrenoceptors | A | pKi | 7.4 | 7.4 | 7.4 | ChEMBL |
α2A | ADA2A | Human | Adrenoceptors | A | pKi | 6.28 | 6.28 | 6.28 | ChEMBL |
α2B | ADA2B | Human | Adrenoceptors | A | pKi | 6.08 | 6.08 | 6.08 | ChEMBL |
D2 | DRD2 | Human | Dopamine | A | pKi | 7.11 | 7.11 | 7.11 | ChEMBL |
D4 | DRD4 | Human | Dopamine | A | pKi | 7.96 | 7.96 | 7.96 | ChEMBL |
H1 | HRH1 | Human | Histamine | A | pKi | 6.21 | 6.21 | 6.21 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
M1 | ACM1 | Human | Acetylcholine (muscarinic) | A | pEC50 | 6.13 | 6.4 | 6.82 | ChEMBL |