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ID: ALA2387159
Max Phase: Preclinical
Molecular Formula: C23H18F3N3O3
Molecular Weight: 441.41
Molecule Type: Small molecule
Associated Items:
ID: ALA2387159
Max Phase: Preclinical
Molecular Formula: C23H18F3N3O3
Molecular Weight: 441.41
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCN1C(=O)N(c2ccc(O)cc2)C(=O)N(c2ccccc2)c2cc(C(F)(F)F)ccc21
Standard InChI: InChI=1S/C23H18F3N3O3/c1-2-27-19-13-8-15(23(24,25)26)14-20(19)28(16-6-4-3-5-7-16)22(32)29(21(27)31)17-9-11-18(30)12-10-17/h3-14,30H,2H2,1H3
Standard InChI Key: MDIBRZHIXLGGFE-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: 441.41 | Molecular Weight (Monoisotopic): 441.1300 | AlogP: 6.14 | #Rotatable Bonds: 3 |
Polar Surface Area: 64.09 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
#RO5 Violations: 1 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 8.84 | CX Basic pKa: | CX LogP: 5.00 | CX LogD: 4.98 |
Aromatic Rings: 3 | Heavy Atoms: 32 | QED Weighted: 0.53 | Np Likeness Score: -0.90 |
1. Fader LD, Landry S, Morin S, Kawai SH, Bousquet Y, Hucke O, Goudreau N, Lemke CT, Bonneau P, Titolo S, Mason S, Simoneau B.. (2013) Optimization of a 1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione series of HIV capsid assembly inhibitors 1: addressing configurational instability through scaffold modification., 23 (11): [PMID:23583513] [10.1016/j.bmcl.2013.03.073] |
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