ID: ALA602332

Max Phase: Preclinical

Molecular Formula: C24H23N3O4

Molecular Weight: 417.47

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N/N=C/c2ccccc2)cc1

Standard InChI:  InChI=1S/C24H23N3O4/c1-31-21-13-9-19(10-14-21)23(29)26-22(15-17-7-11-20(28)12-8-17)24(30)27-25-16-18-5-3-2-4-6-18/h2-14,16,22,28H,15H2,1H3,(H,26,29)(H,27,30)/b25-16+/t22-/m0/s1

Standard InChI Key:  IPGILMCMRVMBDB-LWROZRRASA-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: 417.47Molecular Weight (Monoisotopic): 417.1689AlogP: 2.89#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: 1.64CX LogP: 3.62CX LogD: 3.62
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.39Np Likeness Score: -0.75

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