Supuran CT - Search Results

1

A computer-assisted discovery of novel potential anti-obesity compounds as selective carbonic anhydrase VA inhibitors.

Costa G, Carta F, Ambrosio FA, Artese A, Ortuso F, Moraca F, Rocca R, Romeo I, Lupia A, Maruca A, Bagetta D, Catalano R, Vullo D, Alcaro S, Supuran CT. Costa G, et al. Among authors: supuran ct. Eur J Med Chem. 2019 Nov 1;181:111565. doi: 10.1016/j.ejmech.2019.111565. Epub 2019 Jul 27. Eur J Med Chem. 2019. PMID: 31387062

2

Carbonic anhydrase inhibitors: inhibition of isozymes I, II and IV with heterocyclic mercaptans, sulfenamides, sulfonamides and their metal complexes.

Supuran CT, Scozzafava A, Saramet I, Banciu MD. Supuran CT, et al. J Enzyme Inhib. 1998 Jun;13(3):177-94. doi: 10.3109/14756369809028339. J Enzyme Inhib. 1998. PMID: 9629536

3

Carbonic anhydrase inhibitors: inhibition of isozymes I, II and IV with N-hydroxysulfonamides--a novel class of intraocular pressure lowering agents.

Mincione F, Menabuoni L, Briganti F, Mincione G, Scozzafava A, Supuran CT. Mincione F, et al. Among authors: supuran ct. J Enzyme Inhib. 1998 Jul;13(4):267-84. doi: 10.3109/14756369809021475. J Enzyme Inhib. 1998. PMID: 9795865

4

Carbonic anhydrase inhibitors: novel compounds containing S-NH moieties: sulfenamido-sulfonamides, sulfenimido-sulfonamides and their interaction with isozymes I, II and IV.

Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. J Enzyme Inhib. 1998 Sep;13(6):419-42. doi: 10.3109/14756369809020547. J Enzyme Inhib. 1998. PMID: 9825306

5

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

6

Carbonic anhydrase inhibitors. Part 71. Synthesis and ocular pharmacology of a new class of water-soluble, topically effective intraocular pressure lowering sulfonamides incorporating picolinoyl moieties.

Supuran CT, Scozzafava A, Menabuoni L, Mincione F, Briganti F, Mincione G. Supuran CT, et al. Eur J Pharm Sci. 1999 Aug;8(4):317-28. doi: 10.1016/s0928-0987(99)00022-6. Eur J Pharm Sci. 1999. PMID: 10425382

7

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

8

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

9

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

10

Carbonic anhydrase activators: amino acyl/dipeptidyl histamine derivatives bind with high affinity to isozymes I, II and IV and act as efficient activators.

Supuran CT, Scozzafava A. Supuran CT, et al. Bioorg Med Chem. 1999 Dec;7(12):2915-23. doi: 10.1016/s0968-0896(99)00227-8. Bioorg Med Chem. 1999. PMID: 10658596

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