ID: ALA183099

Max Phase: Preclinical

Molecular Formula: C21H26N4O3

Molecular Weight: 382.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CO/N=C/c1ccc(OCCCCCN2CCN(c3ccncc3)C2=O)cc1

Standard InChI:  InChI=1S/C21H26N4O3/c1-27-23-17-18-5-7-20(8-6-18)28-16-4-2-3-13-24-14-15-25(21(24)26)19-9-11-22-12-10-19/h5-12,17H,2-4,13-16H2,1H3/b23-17+

Standard InChI Key:  BONNYJTYPIAEFC-HAVVHWLPSA-N

Associated Targets(Human)

Rhabdomyosarcoma cell 40 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Enterovirus A71 1246 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: 382.46Molecular Weight (Monoisotopic): 382.2005AlogP: 3.55#Rotatable Bonds: 10
Polar Surface Area: 67.26Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.54CX LogP: 2.57CX LogD: 2.56
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.36Np Likeness Score: -1.46

References

1. Chern JH, Lee CC, Chang CS, Lee YC, Tai CL, Lin YT, Shia KS, Lee CY, Shih SR..  (2004)  Synthesis and antienteroviral activity of a series of novel, oxime ether-containing pyridyl imidazolidinones.,  14  (20): [PMID:15380197] [10.1016/j.bmcl.2004.07.084]

Source