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Inhibition of carbonic anhydrase isozymes with benzene sulfonamides incorporating thio, sulfinyl and sulfonyl glycoside moieties

Title: Inhibition of carbonic anhydrase isozymes with benzene sulfonamides incorporating thio, sulfinyl and sulfonyl glycoside moieties
Authors: Singer, Mathilde; Lopez, Marie; Bornaghi, Laurent F; Innocenti, Alessio; Vullo, Daniela; Supuran, Claudiu T; Poulsen, Sally-Ann
Publisher Information: Elsevier
Publication Year: 2009
Collection: Griffith University: Griffith Research Online
Subject Terms: Medicinal and biomolecular chemistry; Biologically active molecules; Organic chemistry; Pharmacology and pharmaceutical sciences
Description: A series of benzene sulfonamides incorporating thio, sulfinyl or sulfonyl glycoside moieties were synthesized. These glycoconjugates were investigated for their ability to inhibit the enzymatic activity of four human carbonic anhydrases (hCA): isozymes I, II and tumour-associated isozymes IX and XII. The oxidation state of the sulfur in the carbohydrate tail moiety did not influence either enzyme inhibition potency or isozyme selectivity even though presenting opportunities for differing interactions with the target isozymes. ; Griffith Sciences, Griffith Institute for Drug Discovery ; Full Text
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: Bioorganic and Medicinal Chemistry Letters; http://www.sciencedirect.com/science/journal/0960894X; https://hdl.handle.net/10072/29582
DOI: 10.1016/j.bmcl.2009.02.086
Availability: https://hdl.handle.net/10072/29582; https://doi.org/10.1016/j.bmcl.2009.02.086
Rights: © 2009 Elsevier. This is the author-manuscript version of this paper. Reproduced in accordance with the copyright policy of the publisher. Please refer to the journal's website for access to the definitive, published version. ; open access
Accession Number: edsbas.BF87F3B0
Database: BASE