Supuran CT - Search Results

1

Dual Cyclooxygenase and Carbonic Anhydrase Inhibition by Nonsteroidal Anti-Inflammatory Drugs for the Treatment of Cancer.

De Monte C, Carradori S, Gentili A, Mollica A, Trisciuoglio D, Supuran CT. De Monte C, et al. Among authors: supuran ct. Curr Med Chem. 2015;22(24):2812-8. doi: 10.2174/0929867322666150716113501. Curr Med Chem. 2015. PMID: 26180003 Review.

2

Carbonic anhydrase inhibitors. Synthesis of water-soluble, topically effective, intraocular pressure-lowering aromatic/heterocyclic sulfonamides containing cationic or anionic moieties: is the tail more important than the ring?

Scozzafava A, Menabuoni L, Mincione F, Briganti F, Mincione G, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. J Med Chem. 1999 Jul 15;42(14):2641-50. doi: 10.1021/jm9900523. J Med Chem. 1999. PMID: 10411484

3

Carbonic anhydrase inhibitors: synthesis of water-soluble, aminoacyl/dipeptidyl sulfonamides possessing long-lasting intraocular pressure-lowering properties via the topical route.

Scozzafava A, Briganti F, Mincione G, Menabuoni L, Mincione F, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. J Med Chem. 1999 Sep 9;42(18):3690-700. doi: 10.1021/jm9901879. J Med Chem. 1999. PMID: 10479300

4

Carbonic anhydrase inhibitors: synthesis of membrane-impermeant low molecular weight sulfonamides possessing in vivo selectivity for the membrane-bound versus cytosolic isozymes.

Scozzafava A, Briganti F, Ilies MA, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. J Med Chem. 2000 Jan 27;43(2):292-300. doi: 10.1021/jm990479+. J Med Chem. 2000. PMID: 10649985

5

Carbonic anhydrase inhibitors: topical sulfonamide antiglaucoma agents incorporating secondary amine moieties.

Renzi G, Scozzafava A, Supuran CT. Renzi G, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2000 Apr 3;10(7):673-6. doi: 10.1016/s0960-894x(00)00075-5. Bioorg Med Chem Lett. 2000. PMID: 10762051

6

Carbonic anhydrase inhibitors - part 78(#). Synthesis of water-soluble sulfonamides incorporating beta-alanyl moieties, possessing long lasting-intraocular pressure lowering properties via the topical route.

Supuran CT, Briganti F, Menabuoni L, Mincione G, Mincione F, Scozzafava A. Supuran CT, et al. Eur J Med Chem. 2000 Mar;35(3):309-21. doi: 10.1016/s0223-5234(00)00130-6. Eur J Med Chem. 2000. PMID: 10785557

7

Carbonic anhydrase inhibitors: sulfonamides incorporating furan-, thiophene- and pyrrole-carboxamido groups possess strong topical intraocular pressure lowering properties as aqueous suspensions.

Ilies M, Supuran CT, Scozzafava A, Casini A, Mincione F, Menabuoni L, Caproiu MT, Maganu M, Banciu MD. Ilies M, et al. Among authors: supuran ct. Bioorg Med Chem. 2000 Aug;8(8):2145-55. doi: 10.1016/s0968-0896(00)00143-7. Bioorg Med Chem. 2000. PMID: 11003159

8

Carbonic anhydrase inhibitors. Part 86. A QSAR study on some sulfonamide drugs which lower intra-ocular pressure, using the ACE non-linear statistical method.

Clare BW, Supuran CT. Clare BW, et al. Among authors: supuran ct. Eur J Med Chem. 2000 Sep;35(9):859-65. doi: 10.1016/s0223-5234(00)00182-3. Eur J Med Chem. 2000. PMID: 11006487

9

Carbonic anhydrase and matrix metalloproteinase inhibitors: sulfonylated amino acid hydroxamates with MMP inhibitory properties act as efficient inhibitors of CA isozymes I, II, and IV, and N-hydroxysulfonamides inhibit both these zinc enzymes.

Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. J Med Chem. 2000 Oct 5;43(20):3677-87. doi: 10.1021/jm000027t. J Med Chem. 2000. PMID: 11020282

10

Carbonic anhydrase inhibitors: perfluoroalkyl/aryl-substituted derivatives of aromatic/heterocyclic sulfonamides as topical intraocular pressure-lowering agents with prolonged duration of action.

Scozzafava A, Menabuoni L, Mincione F, Briganti F, Mincione G, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. J Med Chem. 2000 Nov 16;43(23):4542-51. doi: 10.1021/jm000296j. J Med Chem. 2000. PMID: 11087579

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