ID: ALA3288456
Chembl Id: CHEMBL3288456
PubChem CID: 90681225
Max Phase: Preclinical
Molecular Formula: C16H17ClN2
Molecular Weight: 272.78
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CN(C)C/C=C(/c1cccc(Cl)c1)c1ccccn1
Standard InChI: InChI=1S/C16H17ClN2/c1-19(2)11-9-15(16-8-3-4-10-18-16)13-6-5-7-14(17)12-13/h3-10,12H,11H2,1-2H3/b15-9-
Standard InChI Key: JWNCVTVQWCNGOK-DHDCSXOGSA-N
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| 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 |
|---|
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| Molecular Weight: 272.78 | Molecular Weight (Monoisotopic): 272.1080 | AlogP: 3.73 | #Rotatable Bonds: 4 |
| Polar Surface Area: 16.13 | Molecular Species: BASE | HBA: 2 | HBD: ┄ |
| #RO5 Violations: ┄ | HBA (Lipinski): 2 | HBD (Lipinski): ┄ | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: ┄ | CX Basic pKa: 8.54 | CX LogP: 3.73 | CX LogD: 2.56 |
| Aromatic Rings: 2 | Heavy Atoms: 19 | QED Weighted: 0.84 | Np Likeness Score: -0.93 |
| 1. Deane KJ, Summers RL, Lehane AM, Martin RE, Barrow RA.. (2014) Chlorpheniramine Analogues Reverse Chloroquine Resistance in Plasmodium falciparum by Inhibiting PfCRT., 5 (5): [PMID:24900883] [10.1021/ml5000228] |
Source(1):
