Inhibition of human carbonic anhydrase isozymes I, II, IX and XII with a new series of sulfonamides incorporating aroylhydrazone-, [1,2,4]triazolo[3,4-b][1,3,4]thiadiazinyl- or 2-(cyanophenylmethylene)-1,3,4-thiadiazol-3(2H)-yl moieties-Reference-Cited by-同舟云学术

Inhibition of human carbonic anhydrase isozymes I, II, IX and XII with a new series of sulfonamides incorporating aroylhydrazone-, [1,2,4]triazolo[3,4-b][1,3,4]thiadiazinyl- or 2-(cyanophenylmethylene)-1,3,4-thiadiazol-3(2H)-yl moieties

Published:2014-03-25 Issue:1 Volume:30 Page:52-56
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:

Alafeefy Ahmed M.,Abdel-Aziz Hatem A.,Vullo Daniela,Al-Tamimi Abdul-Malek S.,Awaad Amani S.,Mohamed Menshawy A.,Capasso Clemente,Supuran Claudiu T.

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/14756366.2013.877897

Reference34 articles.

1. Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

2. Interfering with pH regulation in tumours as a therapeutic strategy

3. Review Article

4. Structure-based drug discovery of carbonic anhydrase inhibitors

5. Bacterial Carbonic Anhydrases as Drug Targets: Toward Novel Antibiotics?

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