Supuran CT - Search Results

1

Structure activity study of carbonic anhydrase IX: Selective inhibition with ureido-substituted benzenesulfonamides.

Mboge MY, Mahon BP, Lamas N, Socorro L, Carta F, Supuran CT, Frost SC, McKenna R. Mboge MY, et al. Among authors: supuran ct. Eur J Med Chem. 2017 May 26;132:184-191. doi: 10.1016/j.ejmech.2017.03.026. Epub 2017 Mar 19. Eur J Med Chem. 2017. PMID: 28363153 Free PMC article.

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

Novel carbonic anhydrase isozymes I, II and IV activators incorporating sulfonyl-histamino moieties.

Briganti F, Scozzafava A, Supuran CT. Briganti F, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 1999 Jul 19;9(14):2043-8. doi: 10.1016/s0960-894x(99)00310-8. Bioorg Med Chem Lett. 1999. PMID: 10450978

4

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

5

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

6

Carbonic anhydrase activators - part 21. Novel activators of isozymes I, II and IV incorporating carboxamido and ureido histamine moieties.

Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. Eur J Med Chem. 2000 Jan;35(1):31-9. doi: 10.1016/s0223-5234(00)00102-1. Eur J Med Chem. 2000. PMID: 10733601

7

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

8

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

9

Protease inhibitors: synthesis and QSAR study of novel classes of nonbasic thrombin inhibitors incorporating sulfonylguanidine and O-methylsulfonylisourea moieties at P1.

Supuran CT, Scozzafava A, Briganti F, Clare BW. Supuran CT, et al. J Med Chem. 2000 May 4;43(9):1793-806. doi: 10.1021/jm9903693. J Med Chem. 2000. PMID: 10794696

10

Carbonic anhydrase inhibitors: synthesis of N-morpholylthiocarbonylsulfenylamino aromatic/heterocyclic sulfonamides and their interaction with isozymes I, II and IV.

Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2000 May 15;10(10):1117-20. doi: 10.1016/s0960-894x(00)00178-5. Bioorg Med Chem Lett. 2000. PMID: 10843231

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