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Inhibition and binding studies of carbonic anhydrase isozymes I, II and IX with benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulphonamides.
Baranauskienė L, Hilvo M, Matulienė J, Golovenko D, Manakova E, Dudutienė V, Michailovienė V, Torresan J, Jachno J, Parkkila S, Maresca A, Supuran CT, Gražulis S, Matulis D. Baranauskienė L, et al. Among authors: maresca a. J Enzyme Inhib Med Chem. 2010 Dec;25(6):863-70. doi: 10.3109/14756360903571685. Epub 2010 Feb 18. J Enzyme Inhib Med Chem. 2010. PMID: 20166809
Carbonic anhydrase inhibitors. Synthesis of 2,4,6-trimethylpyridinium derivatives of 2-(hydrazinocarbonyl)-3-aryl-1H-indole-5-sulfonamides acting as potent inhibitors of the tumor-associated isoform IX and XII.
Güzel O, Maresca A, Scozzafava A, Salman A, Balaban AT, Supuran CT. Güzel O, et al. Among authors: maresca a. Bioorg Med Chem Lett. 2009 Jun 1;19(11):2931-4. doi: 10.1016/j.bmcl.2009.04.068. Epub 2009 Apr 22. Bioorg Med Chem Lett. 2009. PMID: 19410461
Carbonic anhydrase inhibitors. The X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitors.
Avvaru BS, Wagner JM, Maresca A, Scozzafava A, Robbins AH, Supuran CT, McKenna R. Avvaru BS, et al. Among authors: maresca a. Bioorg Med Chem Lett. 2010 Aug 1;20(15):4376-81. doi: 10.1016/j.bmcl.2010.06.082. Epub 2010 Jun 17. Bioorg Med Chem Lett. 2010. PMID: 20605094
266 results