(Z)-N-(4-(4-Chlorophenoxy)phenyl)-2-(5-(2,3-dihydroxybenzylidene)-4-oxo-2-thioxothiazolidin-3-yl)acetamide

ID: ALA3309761

PubChem CID: 118706081

Max Phase: Preclinical

Molecular Formula: C24H17ClN2O5S2

Molecular Weight: 513.00

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(CN1C(=O)/C(=C/c2cccc(O)c2O)SC1=S)Nc1ccc(Oc2ccc(Cl)cc2)cc1

Standard InChI:  InChI=1S/C24H17ClN2O5S2/c25-15-4-8-17(9-5-15)32-18-10-6-16(7-11-18)26-21(29)13-27-23(31)20(34-24(27)33)12-14-2-1-3-19(28)22(14)30/h1-12,28,30H,13H2,(H,26,29)/b20-12-

Standard InChI Key:  DHOBLLZJXRUGFB-NDENLUEZSA-N

Molfile:  

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M  END

Alternative Forms

  1. Parent:

    ALA3309761

    ---

Associated Targets(non-human)

dxr 1-deoxyxylulose-5-phosphate reductoisomerase (147 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
mdh Malate dehydrogenase (29 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

Calculated Properties

Molecular Weight: 513.00Molecular Weight (Monoisotopic): 512.0267AlogP: 5.38#Rotatable Bonds: 6
Polar Surface Area: 99.10Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 9.09CX Basic pKa: CX LogP: 5.37CX LogD: 5.36
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.23Np Likeness Score: -1.55

References

1. Zinglé C, Tritsch D, Grosdemange-Billiard C, Rohmer M..  (2014)  Catechol-rhodanine derivatives: Specific and promiscuous inhibitors of Escherichia coli deoxyxylulose phosphate reductoisomerase (DXR).,  22  (14): [PMID:24890653] [10.1016/j.bmc.2014.05.004]

Source