Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4437337
Max Phase: Preclinical
Molecular Formula: C12H9ClN2O
Molecular Weight: 232.67
Molecule Type: Unknown
Associated Items:
ID: ALA4437337
Max Phase: Preclinical
Molecular Formula: C12H9ClN2O
Molecular Weight: 232.67
Molecule Type: Unknown
Associated Items:
Canonical SMILES: O=C(Nc1ccncc1)c1cccc(Cl)c1
Standard InChI: InChI=1S/C12H9ClN2O/c13-10-3-1-2-9(8-10)12(16)15-11-4-6-14-7-5-11/h1-8H,(H,14,15,16)
Standard InChI Key: AGEMHBDIONALQA-UHFFFAOYSA-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: Unknown | 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: 232.67 | Molecular Weight (Monoisotopic): 232.0403 | AlogP: 2.99 | #Rotatable Bonds: 2 |
Polar Surface Area: 41.99 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 5.62 | CX LogP: 2.45 | CX LogD: 2.45 |
Aromatic Rings: 2 | Heavy Atoms: 16 | QED Weighted: 0.87 | Np Likeness Score: -2.05 |
1. Wicht KJ, Combrinck JM, Smith PJ, Hunter R, Egan TJ.. (2016) Identification and SAR Evaluation of Hemozoin-Inhibiting Benzamides Active against Plasmodium falciparum., 59 (13): [PMID:27299916] [10.1021/acs.jmedchem.6b00719] |
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