Synthesis and carbonic anhydrase I, II, VII, and IX inhibition studies with a series of benzo[d]thiazole-5- and 6-sulfonamides

A series of benzo[d]thiazole-5- and 6-sulfonamides has been synthesized and investigated for the inhibition of several human (h) carbonic anhydrase (CA, EC 4.2.1.1) isoforms, using ethoxzolamide (EZA) as lead molecule. 2-Amino-substituted, 2-acylamino- and halogenated (bromo-and iodo-derivatives at...

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Detalhes bibliográficos
Publicado no:J Enzyme Inhib Med Chem
Main Authors: Abdoli, Morteza, Angeli, Andrea, Bozdag, Murat, Carta, Fabrizio, Kakanejadifard, Ali, Saeidian, Hamid, Supuran, Claudiu T.
Formato: Artigo
Idioma:Inglês
Publicado em: Taylor & Francis 2017
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6010138/
https://ncbi.nlm.nih.gov/pubmed/28753093
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/14756366.2017.1356295
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