ID: ALA590029

Max Phase: Preclinical

Molecular Formula: C24H22ClN3O4

Molecular Weight: 451.91

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N/N=C/c2ccc(Cl)cc2)cc1

Standard InChI:  InChI=1S/C24H22ClN3O4/c1-32-21-12-6-18(7-13-21)23(30)27-22(14-16-4-10-20(29)11-5-16)24(31)28-26-15-17-2-8-19(25)9-3-17/h2-13,15,22,29H,14H2,1H3,(H,27,30)(H,28,31)/b26-15+/t22-/m0/s1

Standard InChI Key:  BAIAJKCTBNBHFB-WGLQLPMYSA-N

Associated Targets(non-human)

Simian immunodeficiency virus 338 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: 451.91Molecular Weight (Monoisotopic): 451.1299AlogP: 3.55#Rotatable Bonds: 8
Polar Surface Area: 100.02Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.50CX Basic pKa: 1.27CX LogP: 4.23CX LogD: 4.22
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.36Np Likeness Score: -0.90

References

1. Jin Y, Tan Z, He M, Tian B, Tang S, Hewlett I, Yang M..  (2010)  SAR and molecular mechanism study of novel acylhydrazone compounds targeting HIV-1 CA.,  18  (6): [PMID:20188575] [10.1016/j.bmc.2010.02.003]

Source