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TitleA thiabendazole sulfonamide shows potent inhibitory activity against mammalian and nematode alpha-carbonic anhydrases
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 19, Page 1371-1375, Year 2009
Publish dateDec 4, 2008 (structure data deposition date)
AuthorsCrocetti, L. / Maresca, A. / Temperini, C. / Hall, R.A. / Scozzafava, A. / Muhlschlegel, F.A. / Supuran, C.T.
External linksBioorg. Med. Chem. Lett. / PubMed:19186056
MethodsX-ray diffraction
Resolution1.81 Å
Structure data

PDB-3ffp:
X ray structure of the complex between carbonic anhydrase II and LC inhibitors
Method: X-RAY DIFFRACTION / Resolution: 1.81 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-HG:
Unknown entry

ChemComp-LC1:
2-(1,3-thiazol-4-yl)-1H-benzimidazole-5-sulfonamide

ChemComp-BEZ:
BENZOIC ACID

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsLYASE / carbonic anhydrase / inhibitors / Acetylation / Cytoplasm / Disease mutation / Metal-binding / Polymorphism / Zinc

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