Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/22912
Title: Inhibition of membrane-associated carbonic anhydrase isozymes IX, XII and XIV with a library of glycoconjugate benzenesulfonamides
Contributor(s): Wilkinson, Brendan (author)orcid ; Bornaghi, Laurent F (author); Houston, Todd A (author); Innocenti, Alessio (author); Vullo, Daniela (author); Supuran, Claudiu T (author); Poulsen, Sally-Ann (author)
Publication Date: 2007
DOI: 10.1016/j.bmcl.2006.11.046
Handle Link: https://hdl.handle.net/1959.11/22912
Abstract: A library of glycoconjugate benzenesulfonamides that contain diverse carbohydrate-triazole tails were investigated for their ability to inhibit the enzymatic activity of the three human transmembrane carbonic anhydrase (CA) isozymes hCA IX, hCA XII and hCA XIV. These isozymes have their CA domains located extracellularly, unlike the physiologically dominant hCA II, and are of immense current interest as druggable targets. Elevated expression of isozymes IX and XII is a marker for a broad spectrum of hypoxic tumors-this physiology may facilitate a novel approach to discriminate between healthy cells and cancerous cells. Many of these glycoconjugates were potent inhibitors (low nM), but importantly exhibited different isozyme selectivity profiles. The most potent hCA IX inhibitor was the glucuronic acid derivative 20 (Kᵢ = 23 nM). This compound was uniquely hCA IX selective cf. all other isozymes (16.4-, 16.8- and 4.6-fold selective against hCA II, XII, and XIV, respectively). At hCA XII there were many inhibitors with Kᵢs < 10 nM that also demonstrated excellent selectivity (up to 344-fold) against other isozymes. Potent hCA XIV inhibitors were also identified, several with Kᵢs ~ 10 nM, however no hCA XIV-selective derivatives were evidenced from this library. The sugar tails of this study have shown promise as a valuable approach to both solubilize the aromatic sulfonamide CA recognition pharmacophore and to deliver potent inhibition and isozyme differentiation of the transmembrane CAs.
Publication Type: Journal Article
Source of Publication: Bioorganic & Medicinal Chemistry Letters, 17(4), p. 987-992
Publisher: Pergamon Press
Place of Publication: United Kingdom
ISSN: 1464-3405
0960-894X
Field of Research (FOR): 030499 Medicinal and Biomolecular Chemistry not elsewhere classified
030401 Biologically Active Molecules
030503 Organic Chemical Synthesis
Peer Reviewed: Yes
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
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