ID: ALA3758565
Chembl Id: CHEMBL3758565
PubChem CID: 68845701
Max Phase: Preclinical
Molecular Formula: C12H15N
Molecular Weight: 173.26
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1cccc(C2=NCCCC2)c1
Standard InChI: InChI=1S/C12H15N/c1-10-5-4-6-11(9-10)12-7-2-3-8-13-12/h4-6,9H,2-3,7-8H2,1H3
Standard InChI Key: BUUFQMSIVSLYGH-UHFFFAOYSA-N
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| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Molecular Weight: 173.26 | Molecular Weight (Monoisotopic): 173.1204 | AlogP: 2.97 | #Rotatable Bonds: 1 |
| Polar Surface Area: 12.36 | Molecular Species: BASE | HBA: 1 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 1 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 8.76 | CX LogP: 2.95 | CX LogD: 1.57 |
| Aromatic Rings: 1 | Heavy Atoms: 13 | QED Weighted: 0.62 | Np Likeness Score: -0.83 |
| 1. Matera C, Quadri M, Sciaccaluga M, Pomè DY, Fasoli F, De Amici M, Fucile S, Gotti C, Dallanoce C, Grazioso G.. (2016) Modification of the anabaseine pyridine nucleus allows achieving binding and functional selectivity for the α3β4 nicotinic acetylcholine receptor subtype., 108 [PMID:26706350] [10.1016/j.ejmech.2015.11.045] |
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