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TitleIdentification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as Potent Carbonic Anhydrase Inhibitors: Synthesis, Biological Evaluation, and Enzyme-Ligand X-ray Studies.
Journal, issue, pagesJ. Med. Chem., Year 2010
Publish dateJul 28, 2009 (structure data deposition date)
AuthorsGitto, R. / Agnello, S. / Ferro, S. / De Luca, L. / Vullo, D. / Brynda, J. / Mader, P. / Supuran, C.T. / Chimirri, A.
External linksJ. Med. Chem. / PubMed:20170095
MethodsX-ray diffraction
Resolution1.65 Å
Structure data

PDB-3igp:
Structure of inhibitor binding to Carbonic Anhydrase II
Method: X-RAY DIFFRACTION / Resolution: 1.65 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-DT7:
6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-sulfonamide

ChemComp-GOL:
GLYCEROL

ChemComp-HOH:
WATER

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

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