ID: ALA3623550
Chembl Id: CHEMBL3623550
PubChem CID: 107886865
Max Phase: Preclinical
Molecular Formula: C10H13F3N2O
Molecular Weight: 234.22
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCC(C)n1cc(C(=O)C(F)(F)F)cn1
Standard InChI: InChI=1S/C10H13F3N2O/c1-3-4-7(2)15-6-8(5-14-15)9(16)10(11,12)13/h5-7H,3-4H2,1-2H3
Standard InChI Key: QWJQWXDSWXGISZ-UHFFFAOYSA-N
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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: 234.22 | Molecular Weight (Monoisotopic): 234.0980 | AlogP: 2.99 | #Rotatable Bonds: 4 |
| Polar Surface Area: 34.89 | Molecular Species: NEUTRAL | HBA: 3 | HBD: ┄ |
| #RO5 Violations: ┄ | HBA (Lipinski): 3 | HBD (Lipinski): ┄ | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: ┄ | CX Basic pKa: 1.06 | CX LogP: 2.83 | CX LogD: 2.83 |
| Aromatic Rings: 1 | Heavy Atoms: 16 | QED Weighted: 0.75 | Np Likeness Score: -1.27 |
| 1. Camerino E, Wong DM, Tong F, Körber F, Gross AD, Islam R, Viayna E, Mutunga JM, Li J, Totrov MM, Bloomquist JR, Carlier PR.. (2015) Difluoromethyl ketones: Potent inhibitors of wild type and carbamate-insensitive G119S mutant Anopheles gambiae acetylcholinesterase., 25 (20): [PMID:26386602] [10.1016/j.bmcl.2015.09.019] |
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