ID: ALA605614

Max Phase: Preclinical

Molecular Formula: C22H27N3O3

Molecular Weight: 381.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCC(C)[C@H](NC(=O)c1ccc(OC)cc1)C(=O)N/N=C/c1ccc(C)cc1

Standard InChI:  InChI=1S/C22H27N3O3/c1-5-16(3)20(24-21(26)18-10-12-19(28-4)13-11-18)22(27)25-23-14-17-8-6-15(2)7-9-17/h6-14,16,20H,5H2,1-4H3,(H,24,26)(H,25,27)/b23-14+/t16?,20-/m0/s1

Standard InChI Key:  PNBNTYSIOLVYHG-BAKBTDCSSA-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: 381.48Molecular Weight (Monoisotopic): 381.2052AlogP: 3.30#Rotatable Bonds: 8
Polar Surface Area: 79.79Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.66CX Basic pKa: 1.96CX LogP: 4.11CX LogD: 4.11
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.54Np Likeness Score: -1.15

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