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Glaucoma and the applications of carbonic anhydrase inhibitors.
Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. Subcell Biochem. 2014;75:349-59. doi: 10.1007/978-94-007-7359-2_17. Subcell Biochem. 2014. PMID: 24146387 Review.
Carbonic anhydrase activators: high affinity isozymes I, II, and IV activators, incorporating a beta-alanyl-histidine scaffold.
Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. J Med Chem. 2002 Jan 17;45(2):284-91. doi: 10.1021/jm010958k. J Med Chem. 2002. PMID: 11784133
Carbonic anhydrase inhibitors: anticonvulsant sulfonamides incorporating valproyl and other lipophilic moieties.
Masereel B, Rolin S, Abbate F, Scozzafava A, Supuran CT. Masereel B, et al. Among authors: supuran ct. J Med Chem. 2002 Jan 17;45(2):312-20. doi: 10.1021/jm0109199. J Med Chem. 2002. PMID: 11784136
Carbonic anhydrase activators: design of high affinity isozymes I, II, and IV activators, incorporating tri-/tetrasubstituted-pyridinium-azole moieties.
Ilies M, Banciu MD, Ilies MA, Scozzafava A, Caproiu MT, Supuran CT. Ilies M, et al. Among authors: supuran ct. J Med Chem. 2002 Jan 17;45(2):504-10. doi: 10.1021/jm011031n. J Med Chem. 2002. PMID: 11784154
Carbonic anhydrase inhibitors. A general approach for the preparation of water-soluble sulfonamides incorporating polyamino-polycarboxylate tails and of their metal complexes possessing long-lasting, topical intraocular pressure-lowering properties.
Scozzafava A, Menabuoni L, Mincione F, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. J Med Chem. 2002 Mar 28;45(7):1466-76. doi: 10.1021/jm0108202. J Med Chem. 2002. PMID: 11906288
Carbonic anhydrase activators: human isozyme II is strongly activated by oligopeptides incorporating the carboxyterminal sequence of the bicarbonate anion exchanger AE1.
Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2002 Apr 22;12(8):1177-80. doi: 10.1016/s0960-894x(02)00121-x. Bioorg Med Chem Lett. 2002. PMID: 11934582
Crystal structure of a zinc-activated variant of human carbonic anhydrase I, CA I Michigan 1: evidence for a second zinc binding site involving arginine coordination.
Ferraroni M, Tilli S, Briganti F, Chegwidden WR, Supuran CT, Wiebauer KE, Tashian RE, Scozzafava A. Ferraroni M, et al. Among authors: supuran ct. Biochemistry. 2002 May 21;41(20):6237-44. doi: 10.1021/bi0120446. Biochemistry. 2002. PMID: 12009884
Carbonic anhydrase inhibitors. Preparation of potent sulfonamides inhibitors incorporating bile acid tails.
Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2002 Jun 17;12(12):1551-7. doi: 10.1016/s0960-894x(02)00252-4. Bioorg Med Chem Lett. 2002. PMID: 12039560
Bacterial protease inhibitors.
Supuran CT, Scozzafava A, Clare BW. Supuran CT, et al. Med Res Rev. 2002 Jul;22(4):329-72. doi: 10.1002/med.10007. Med Res Rev. 2002. PMID: 12111749 Review.
Nonaromatic sulfonamide group as an ideal anchor for potent human carbonic anhydrase inhibitors: role of hydrogen-bonding networks in ligand binding and drug design.
Abbate F, Supuran CT, Scozzafava A, Orioli P, Stubbs MT, Klebe G. Abbate F, et al. Among authors: supuran ct. J Med Chem. 2002 Aug 15;45(17):3583-7. doi: 10.1021/jm011131t. J Med Chem. 2002. PMID: 12166931
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