Amide derivatives with pyrazole carboxylic acids of 5-amino-1,3,4-thiadiazole 2-sulfonamide as new carbonic anhydrase inhibitors: Synthesis and investigation of inhibitory effects-Reference-Cited by-同舟云学术

Amide derivatives with pyrazole carboxylic acids of 5-amino-1,3,4-thiadiazole 2-sulfonamide as new carbonic anhydrase inhibitors: Synthesis and investigation of inhibitory effects

Published:2008-01-01 Issue:6 Volume:23 Page:895-900
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Bülbül Metiˇn¹,Kasimoğullari Rahmiˇ¹,Küfreviˇoğlu Ö. Iˇrfan²

Affiliation:

1. Department of Chemistry, Faculty of Science and Arts, Dumlupinar University, 43100, Kutahya, Turkey

2. Department of Chemistry, Faculty of Science and Arts, Ataturk University, 25240, Erzurum, Turkey

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14756360701626173

Reference31 articles.

1. Bile acid derivatives of 5-amino-1,3,4-thiadiazole-2-sulfonamide as new carbonic anhydrase inhibitors: synthesis and investigation of inhibition effects

2. Carbonic Anhydrase Inhibitors

3. Carbonic anhydrase and matrix metalloproteinase inhibitors. Inhibition of human tumor-associated isozymes IX and cytosolic isozyme I and II with sulfonylated hydroxamates

4. Corrigendum to “An evaluation of cytosolic erythrocyte carbonic anhydrase and catalase in carcinoma patients: An elevation of carbonic anhydrase activity” [Clin. Biochem. 39 (2006) 804–809]

5. Carbonic anhydrases as targets for medicinal chemistry

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