Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX

Abbate, F, Casini, Angela ORCID: https://orcid.org/0000-0003-1599-9542, Owa, T, Scozzafava, A and Supuran, C. T. 2004. Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX. Biorganic and Medicinal Chemistry Letters 14 (1) , pp. 217-223. 10.1016/j.bmcl.2003.09.062

Full text not available from this repository.

Abstract

E7070 [N-(3-chloro-7-indolyl)-1,4-benzenedisulfonamide] is an anticancer drug candidate under clinical development for the treatment of several types of cancers. We prove here that this compound also acts as a potent carbonic anhydrase (CA) inhibitor. Similarly to the clinically used drugs acetazolamide, methazolamide and topiramate, E7070 showed inhibition constants in the range of 15-31 nM against isozymes I, II and IX, being slightly less effective as a CA IV inhibitor (Ki of 65 nM). The X-ray crystal structure of the adduct of hCA II with E7070 revealed unprecedented interactions between the inhibitor and the active site, with three different conformations of the chloroindole fragment of the inhibitor interacting with different amino acid residues/water molecules of the enzyme. A superimposition of these conformations with those of other sulfonamide/sulfamate CA inhibitors indicated that similar regions of the hCA II active site could be involved in the interaction with inhibitors.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Schools > Chemistry
Subjects:	Q Science > QD Chemistry
Uncontrolled Keywords:	Animals; Antigens, Neoplasm; Antineoplastic Agents; Binding Sites; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cattle; Crystallography, X-Ray; Cytosol; Humans; Isoenzymes; Sulfonamides
Publisher:	Elsevier
ISSN:	0960-894X
Last Modified:	31 Oct 2022 10:38
URI:	https://orca.cardiff.ac.uk/id/eprint/85539

Citation Data

Cited 262 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item