Supuran CT - Search Results

1

Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors.

Truppo E, Supuran CT, Sandomenico A, Vullo D, Innocenti A, Di Fiore A, Alterio V, De Simone G, Monti SM. Truppo E, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2012 Feb 15;22(4):1560-4. doi: 10.1016/j.bmcl.2011.12.134. Epub 2012 Jan 5. Bioorg Med Chem Lett. 2012. PMID: 22277279

2

Novel aromatic/heterocyclic sulfonamides and their metal complexes as inhibitors of carbonic anhydrase isozymes I, II and IV.

Supuran CT, Scozzafava A. Supuran CT, et al. J Enzyme Inhib. 1997 Apr;12(1):37-51. doi: 10.3109/14756369709027662. J Enzyme Inhib. 1997. PMID: 9204381

3

Sulfenamido-sulfonamides as inhibitors of carbonic anhydrase isozymes I, II and IV.

Supuran CT, Briganti F, Scozzafava A. Supuran CT, et al. J Enzyme Inhib. 1997 Aug;12(3):175-90. doi: 10.3109/14756369709029313. J Enzyme Inhib. 1997. PMID: 9314114

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: N-cyanosulfonamides, a new class of high affinity isozyme II and IV inhibitors.

Supuran CT, Scozzafava A, Briganti F. Supuran CT, et al. J Enzyme Inhib. 1999;14(4):289-306. doi: 10.3109/14756369909030323. J Enzyme Inhib. 1999. PMID: 10445050

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 water-soluble, topically effective intraocular pressure lowering aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties: is the tail more important than the ring?

Borras J, Scozzafava A, Menabuoni L, Mincione F, Briganti F, Mincione G, Supuran CT. Borras J, et al. Among authors: supuran ct. Bioorg Med Chem. 1999 Nov;7(11):2397-406. doi: 10.1016/s0968-0896(99)00190-x. Bioorg Med Chem. 1999. PMID: 10632049

10

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

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