Supuran CT - Search Results

1

Novel 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide based thiosemicarbazides as potent and selective inhibitors of tumor-associated human carbonic anhydrase IX and XII: Synthesis, cytotoxicity, and molecular modelling studies.

Demir-Yazıcı K, Trawally M, Bua S, Öztürk-Civelek D, Akdemir A, Supuran CT, Güzel-Akdemir Ö. Demir-Yazıcı K, et al. Among authors: supuran ct. Bioorg Chem. 2024 Mar;144:107096. doi: 10.1016/j.bioorg.2024.107096. Epub 2024 Jan 23. Bioorg Chem. 2024. PMID: 38290186

2

Carbonic anhydrase inhibitors: sulfonamides as antitumor agents?

Supuran CT, Briganti F, Tilli S, Chegwidden WR, Scozzafava A. Supuran CT, et al. Bioorg Med Chem. 2001 Mar;9(3):703-14. doi: 10.1016/s0968-0896(00)00288-1. Bioorg Med Chem. 2001. PMID: 11310605

3

Carbonic anhydrase inhibitors: inhibition of cytosolic isozymes I and II with sulfamide derivatives.

Casini A, Winum JY, Montero JL, Scozzafava A, Supuran CT. Casini A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2003 Mar 10;13(5):837-40. doi: 10.1016/s0960-894x(03)00028-3. Bioorg Med Chem Lett. 2003. PMID: 12617903

4

Carbonic anhydrase inhibitors: SAR and X-ray crystallographic study for the interaction of sugar sulfamates/sulfamides with isozymes I, II and IV.

Casini A, Antel J, Abbate F, Scozzafava A, David S, Waldeck H, Schäfer S, Supuran CT. Casini A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2003 Mar 10;13(5):841-5. doi: 10.1016/s0960-894x(03)00029-5. Bioorg Med Chem Lett. 2003. PMID: 12617904

5

Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozyme IX with aromatic and heterocyclic sulfonamides.

Vullo D, Franchi M, Gallori E, Pastorek J, Scozzafava A, Pastorekova S, Supuran CT. Vullo D, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2003 Mar 24;13(6):1005-9. doi: 10.1016/s0960-894x(03)00091-x. Bioorg Med Chem Lett. 2003. PMID: 12643899

6

Hydroxyurea is a carbonic anhydrase inhibitor.

Scozzafava A, Supuran CT. Scozzafava A, et al. Among authors: supuran ct. Bioorg Med Chem. 2003 May 15;11(10):2241-6. doi: 10.1016/s0968-0896(03)00112-3. Bioorg Med Chem. 2003. PMID: 12713833

7

Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with a bis-sulfonamide-two heads are better than one?

Casini A, Abbate F, Scozzafava A, Supuran CT. Casini A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2003 Aug 18;13(16):2759-63. doi: 10.1016/s0960-894x(03)00508-0. Bioorg Med Chem Lett. 2003. PMID: 12873509

8

Carbonic anhydrase activators. The selective serotonin reuptake inhibitors fluoxetine, sertraline and citalopram are strong activators of isozymes I and II.

Casini A, Caccia S, Scozzafava A, Supuran CT. Casini A, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2003 Aug 18;13(16):2765-8. doi: 10.1016/s0960-894x(03)00507-9. Bioorg Med Chem Lett. 2003. PMID: 12873510

9

Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX.

Abbate F, Casini A, Owa T, Scozzafava A, Supuran CT. Abbate F, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2004 Jan 5;14(1):217-23. doi: 10.1016/j.bmcl.2003.09.062. Bioorg Med Chem Lett. 2004. PMID: 14684331

10

Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with EMATE, a dual inhibitor of carbonic anhydrases and steroid sulfatase.

Abbate F, Winum JY, Potter BV, Casini A, Montero JL, Scozzafava A, Supuran CT. Abbate F, et al. Among authors: supuran ct. Bioorg Med Chem Lett. 2004 Jan 5;14(1):231-4. doi: 10.1016/j.bmcl.2003.09.064. Bioorg Med Chem Lett. 2004. PMID: 14684333

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