ID: ALA360597

Max Phase: Preclinical

Molecular Formula: C23H30N4O3

Molecular Weight: 410.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CO/N=C/c1cc(C)c(OCCCCCN2CCN(c3ccncc3)C2=O)c(C)c1

Standard InChI:  InChI=1S/C23H30N4O3/c1-18-15-20(17-25-29-3)16-19(2)22(18)30-14-6-4-5-11-26-12-13-27(23(26)28)21-7-9-24-10-8-21/h7-10,15-17H,4-6,11-14H2,1-3H3/b25-17+

Standard InChI Key:  QQEKXHKBBAKKNT-KOEQRZSOSA-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: 410.52Molecular Weight (Monoisotopic): 410.2318AlogP: 4.17#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: 4.59CX LogP: 3.59CX LogD: 3.59
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.33Np Likeness Score: -1.29

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