(5Z)-5-[[4-[2-(2,4-dichlorophenoxy)ethoxy]phenyl]methylidene]-1,3-thiazolidine-2,4-dione

ID: ALA2263409

Max Phase: Preclinical

Molecular Formula: C18H13Cl2NO4S

Molecular Weight: 410.28

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1NC(=O)/C(=C/c2ccc(OCCOc3ccc(Cl)cc3Cl)cc2)S1

Standard InChI:  InChI=1S/C18H13Cl2NO4S/c19-12-3-6-15(14(20)10-12)25-8-7-24-13-4-1-11(2-5-13)9-16-17(22)21-18(23)26-16/h1-6,9-10H,7-8H2,(H,21,22,23)/b16-9-

Standard InChI Key:  DPHBLBRFFHICSR-SXGWCWSVSA-N

Associated Targets(Human)

HEp-2 (3859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hemi-diaphragm (24 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: 410.28Molecular Weight (Monoisotopic): 408.9942AlogP: 4.78#Rotatable Bonds: 6
Polar Surface Area: 64.63Molecular Species: ACIDHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.20CX Basic pKa: CX LogP: 4.54CX LogD: 3.39
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.55Np Likeness Score: -1.42

References

1. Prashantha Kumar BR, Santhosh Kumar S, Viral P, Wadhwani A, Vadivelan R, Satish Kumar MN, Elango K, Nanjan MJ.  (2012)  Novel glitazones: glucose uptake and cytotoxic activities, and structureactivity relationships,  21  (9): [10.1007/s00044-011-9792-0]

Source