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Biochemical, structural, and computational studies of a γ-carbonic anhydrase from the pathogenic bacterium Burkholderia pseudomallei.
Di Fiore A, De Luca V, Langella E, Nocentini A, Buonanno M, Monti SM, Supuran CT, Capasso C, De Simone G. Di Fiore A, et al. Among authors: supuran ct. Comput Struct Biotechnol J. 2022 Jul 27;20:4185-4194. doi: 10.1016/j.csbj.2022.07.033. eCollection 2022. Comput Struct Biotechnol J. 2022. PMID: 36016712 Free PMC article.
Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II "selective" inhibitor celecoxib.
Di Fiore A, Pedone C, D'Ambrosio K, Scozzafava A, De Simone G, Supuran CT. Di Fiore A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2006 Jan 15;16(2):437-42. doi: 10.1016/j.bmcl.2005.09.040. Epub 2005 Nov 14. Bioorg Med Chem Lett. 2006. PMID: 16290146
Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of 5-amino-1,3,4-thiadiazole-2-sulfonamide and 5-(4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide to human isoform II.
Menchise V, De Simone G, Di Fiore A, Scozzafava A, Supuran CT. Menchise V, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2006 Dec 15;16(24):6204-8. doi: 10.1016/j.bmcl.2006.09.022. Epub 2006 Sep 26. Bioorg Med Chem Lett. 2006. PMID: 17000110
Carbonic anhydrase inhibitors: binding of an antiglaucoma glycosyl-sulfanilamide derivative to human isoform II and its consequences for the drug design of enzyme inhibitors incorporating sugar moieties.
Di Fiore A, Scozzafava A, Winum JY, Montero JL, Pedone C, Supuran CT, De Simone G. Di Fiore A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2007 Mar 15;17(6):1726-31. doi: 10.1016/j.bmcl.2006.12.099. Epub 2007 Jan 8. Bioorg Med Chem Lett. 2007. PMID: 17251017
2,012 results