| Literature DB >> 19345095 |
Marie-Rose Abdo1, Daniela Vullo, Mohamed-Chiheb Saada, Jean-Louis Montero, Andrea Scozzafava, Jean-Yves Winum, Claudiu T Supuran.
Abstract
Activation of the human carbonic anhydrase (CA, EC 4.2.1.1) isozymes I, II (cytosolic) and IX (transmembrane, tumor-associated isoform) with a series of arylsulfonylhydrazido-l-histidines incorporating 4-substituted-phenyl, pentafluorophenyl- and beta-naphthyl moieties was investigated. The compounds showed a weak hCA I activation profile, but were more efficient as hCA II and IX activators. The 4-iodophenyl-substituted derivative behaved as a strong and isozyme selective hCA II activator, with an activation constant of 0.21muM. This is the first isoform-selective, potent CA activator reported to date.Entities:
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Year: 2009 PMID: 19345095 DOI: 10.1016/j.bmcl.2009.03.050
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823