ID: ALA2387160

Max Phase: Preclinical

Molecular Formula: C24H20F3N3O2

Molecular Weight: 439.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCN1C(=O)N(c2ccc(C)cc2)C(=O)N(c2ccccc2)c2cc(C(F)(F)F)ccc21

Standard InChI:  InChI=1S/C24H20F3N3O2/c1-3-28-20-14-11-17(24(25,26)27)15-21(20)29(18-7-5-4-6-8-18)23(32)30(22(28)31)19-12-9-16(2)10-13-19/h4-15H,3H2,1-2H3

Standard InChI Key:  FRZGEZNFPGNDHS-UHFFFAOYSA-N

Associated Targets(Human)

C8166 1658 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human immunodeficiency virus 1 70413 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Structural capsid protein 291 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 439.44Molecular Weight (Monoisotopic): 439.1508AlogP: 6.74#Rotatable Bonds: 3
Polar Surface Area: 43.86Molecular Species: HBA: 2HBD: 0
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.82CX LogD: 5.82
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.45Np Likeness Score: -1.19

References

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]

Source