ID: ALA2164321
Chembl Id: CHEMBL2164321
PubChem CID: 19172746
Max Phase: Preclinical
Molecular Formula: C15H13Cl2NO3
Molecular Weight: 326.18
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1cccc(OCC(=O)Nc2ccc(Cl)c(Cl)c2)c1
Standard InChI: InChI=1S/C15H13Cl2NO3/c1-20-11-3-2-4-12(8-11)21-9-15(19)18-10-5-6-13(16)14(17)7-10/h2-8H,9H2,1H3,(H,18,19)
Standard InChI Key: DUPSQCUKJBFZQZ-UHFFFAOYSA-N
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| 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: 326.18 | Molecular Weight (Monoisotopic): 325.0272 | AlogP: 4.02 | #Rotatable Bonds: 5 |
| Polar Surface Area: 47.56 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
| #RO5 Violations: ┄ | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: 12.47 | CX Basic pKa: ┄ | CX LogP: 3.78 | CX LogD: 3.78 |
| Aromatic Rings: 2 | Heavy Atoms: 21 | QED Weighted: 0.90 | Np Likeness Score: -1.85 |
| 1. Flipo M, Willand N, Lecat-Guillet N, Hounsou C, Desroses M, Leroux F, Lens Z, Villeret V, Wohlkönig A, Wintjens R, Christophe T, Kyoung Jeon H, Locht C, Brodin P, Baulard AR, Déprez B.. (2012) Discovery of novel N-phenylphenoxyacetamide derivatives as EthR inhibitors and ethionamide boosters by combining high-throughput screening and synthesis., 55 (14): [PMID:22738293] [10.1021/jm300377g] |
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