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Carbonic anhydrase activation and the drug design.
Temperini C, Scozzafava A, Supuran CT. Temperini C, et al. Curr Pharm Des. 2008;14(7):708-15. doi: 10.2174/138161208783877857. Curr Pharm Des. 2008. PMID: 18336317 Review.
Carbonic anhydrase inhibitors: inhibition of human cytosolic isozymes I and II and tumor-associated isozymes IX and XII with S-substituted 4-chloro-2-mercapto-5-methyl-benzenesulfonamides.
Saczewski F, Innocenti A, Sławiński J, Kornicka A, Brzozowski Z, Pomarnacka E, Scozzafava A, Temperini C, Supuran CT. Saczewski F, et al. Among authors: temperini c. Bioorg Med Chem. 2008 Apr 1;16(7):3933-40. doi: 10.1016/j.bmc.2008.01.034. Epub 2008 Jan 26. Bioorg Med Chem. 2008. PMID: 18242998
Carbonic anhydrase inhibitors: clash with Ala65 as a means for designing inhibitors with low affinity for the ubiquitous isozyme II, exemplified by the crystal structure of the topiramate sulfamide analogue.
Winum JY, Temperini C, El Cheikh K, Innocenti A, Vullo D, Ciattini S, Montero JL, Scozzafava A, Supuran CT. Winum JY, et al. Among authors: temperini c. J Med Chem. 2006 Nov 30;49(24):7024-31. doi: 10.1021/jm060807n. J Med Chem. 2006. PMID: 17125255
40 results