Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA1204343
Max Phase: Preclinical
Molecular Formula: C23H31Cl2FN2O
Molecular Weight: 368.50
Molecule Type: Small molecule
Associated Items:
ID: ALA1204343
Max Phase: Preclinical
Molecular Formula: C23H31Cl2FN2O
Molecular Weight: 368.50
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cl.Cl.O[C@@H]1CCN(Cc2ccc(F)cc2)C[C@H]1N1CCC(c2ccccc2)CC1
Standard InChI: InChI=1S/C23H29FN2O.2ClH/c24-21-8-6-18(7-9-21)16-25-13-12-23(27)22(17-25)26-14-10-20(11-15-26)19-4-2-1-3-5-19;;/h1-9,20,22-23,27H,10-17H2;2*1H/t22-,23-;;/m1../s1
Standard InChI Key: FOPXXIUICYTUFQ-TVLOEWINSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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: 368.50 | Molecular Weight (Monoisotopic): 368.2264 | AlogP: 3.64 | #Rotatable Bonds: 4 |
Polar Surface Area: 26.71 | Molecular Species: BASE | HBA: 3 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 8.99 | CX LogP: 3.67 | CX LogD: 2.07 |
Aromatic Rings: 2 | Heavy Atoms: 27 | QED Weighted: 0.89 | Np Likeness Score: -0.70 |
1. Efange SM, Khare A, Parsons SM, Bau R, Metzenthin T.. (1993) Nonsymmetrical bipiperidyls as inhibitors of vesicular acetylcholine storage., 36 (8): [PMID:8478910] [10.1021/jm00060a005] |
Source(1):