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TitleInclusion of a 5-fluorouracil moiety in nitrogenous bases derivatives as human carbonic anhydrase IX and XII inhibitors produced a targeted action against MDA-MB-231 and T47D breast cancer cells.
Journal, issue, pagesEur. J. Med. Chem., Vol. 190, Page 112112-112112, Year 2020
Publish dateJan 14, 2020 (structure data deposition date)
AuthorsPetreni, A. / Bonardi, A. / Lomelino, C. / Osman, S.M. / ALOthman, Z.A. / Eldehna, W.M. / El-Haggar, R. / McKenna, R. / Nocentini, A. / Supuran, C.T.
External linksEur. J. Med. Chem. / PubMed:32044580
MethodsX-ray diffraction
Resolution1.35 Å
Structure data

PDB-6vj3:
Carbonic Anhydrase II in complex with pyrimidine-based inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.35 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-QYA:
2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-N-(4-sulfamoylphenyl)acetamide

ChemComp-GOL:
GLYCEROL

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsLYASE/LYASE INHIBITOR / CA II / Sulfonamide / Pyrimidine / Inhibitor / Cancer / LYASE / LYASE-LYASE INHIBITOR complex

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