ID: ALA2387159

Max Phase: Preclinical

Molecular Formula: C23H18F3N3O3

Molecular Weight: 441.41

Molecule Type: Small molecule

Associated Items:

Representations

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

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: 441.41Molecular Weight (Monoisotopic): 441.1300AlogP: 6.14#Rotatable Bonds: 3
Polar Surface Area: 64.09Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.84CX Basic pKa: CX LogP: 5.00CX LogD: 4.98
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.53Np Likeness Score: -0.90

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