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Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with phosphates, carbamoyl phosphate, and the phosphonate antiviral drug foscarnet.
Rusconi S, Innocenti A, Vullo D, Mastrolorenzo A, Scozzafava A, Supuran CT. Rusconi S, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2004 Dec 6;14(23):5763-7. doi: 10.1016/j.bmcl.2004.09.064. Bioorg Med Chem Lett. 2004. PMID: 15501037
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
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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