ID: ALA3288454
Chembl Id: CHEMBL3288454
PubChem CID: 239424
Max Phase: Preclinical
Molecular Formula: C18H23ClN2
Molecular Weight: 302.85
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCN(CC)CCC(c1ccc(Cl)cc1)c1ccccn1
Standard InChI: InChI=1S/C18H23ClN2/c1-3-21(4-2)14-12-17(18-7-5-6-13-20-18)15-8-10-16(19)11-9-15/h5-11,13,17H,3-4,12,14H2,1-2H3
Standard InChI Key: AZTDPOADIFXROW-UHFFFAOYSA-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: 302.85 | Molecular Weight (Monoisotopic): 302.1550 | AlogP: 4.60 | #Rotatable Bonds: 7 |
| 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: 10.03 | CX LogP: 4.30 | CX LogD: 1.73 |
| Aromatic Rings: 2 | Heavy Atoms: 21 | QED Weighted: 0.74 | Np Likeness Score: -1.40 |
| 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] |
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