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Research Article

Three new aromatic sulfonamide inhibitors of carbonic anhydrases I, II, IV and XII

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Pages 289-293 | Received 20 Nov 2011, Accepted 09 Dec 2011, Published online: 03 Feb 2012

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Süleyman Yılmaz, Yusuf Akbaba, Bünyamin Özgeriş, Leyla Polat Köse, Süleyman Göksu, İlhami Gülçin, Saleh H. Alwasel & Claudiu T. Supuran. (2016) Synthesis and inhibitory properties of some carbamates on carbonic anhydrase and acetylcholine esterase. Journal of Enzyme Inhibition and Medicinal Chemistry 31:6, pages 1484-1491.
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Ozen Ozensoy Guler, Clemente Capasso & Claudiu T. Supuran. (2016) A magnificent enzyme superfamily: carbonic anhydrases, their purification and characterization. Journal of Enzyme Inhibition and Medicinal Chemistry 31:5, pages 689-694.
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Namrata Singasane, Prashant S. Kharkar, Mariangela Ceruso, Claudiu T. Supuran & Mrunmayee P. Toraskar. (2015) Inhibition of carbonic anhydrase isoforms I, II, IX and XII with Schiff’s bases incorporating iminoureido moieties. Journal of Enzyme Inhibition and Medicinal Chemistry 30:6, pages 901-907.
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Mehmet Arslan, Murat Şentürk, İsmail Fidan, Oktay Talaz, Deniz Ekinci, Sedat Coşgun & Claudiu T. Supuran. (2015) Synthesis of 3,4-dihydroxypyrrolidine-2,5-dione and 3,5-dihydroxybenzoic acid derivatives and evaluation of the carbonic anhydrase I and II inhibition. Journal of Enzyme Inhibition and Medicinal Chemistry 30:6, pages 896-900.
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Daniela Vullo, Semra Isik, Murat Bozdag, Fabrizio Carta & Claudiu T. Supuran. (2015) 7-Amino-3,4-dihydro-1H-quinolin-2-one, a compound similar to the substituted coumarins, inhibits α-carbonic anhydrases without hydrolysis of the lactam ring. Journal of Enzyme Inhibition and Medicinal Chemistry 30:5, pages 773-777.
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Chafika Bougheloum, Robila Belghiche & Abdelrani Messalhi. (2015) Synthesis of New Substituted N-Sulfonyl Pyrrolidine-2,5-Dione Using Dawson-Type Heteropolyacid as Catalyst. Phosphorus, Sulfur, and Silicon and the Related Elements 190:3, pages 269-276.
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Lei Zhang, Xuejian Wang, Xiaoguang Li & Wenfang Xu. (2014) Discovery of a series of small molecules as potent histone deacetylase inhibitors. Journal of Enzyme Inhibition and Medicinal Chemistry 29:3, pages 333-337.
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