Carbonic anhydrase inhibitors. Inhibition of the prokariotic beta and gamma-class enzymes from Archaea with sulfonamides

S Zimmerman, A Innocenti, A Casini, JG Ferry, A Scozzafava, CT Supuran*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

76 Citations (Scopus)

Abstract

A detailed inhibition study of carbonic anhydrases (CAs, EC 4.2.1.1) belonging to the beta- and gamma-families from Archaea with sulfonamides has been performed. Compounds included in this study were the clinically used sulfonamide CA inhibitors, such as acetazolamide, methazolamide, ethoxzolamide, topiramate, valdecoxib, celecoxib, dorzolamide, sulfanilamide, dichlorophanamide, as well as sulfanilamide analogs, halogenated sulfanilamides, and some 1,3-benzenedisulfonamide derivatives. The two gamma-CAs from Methanosarcina thermophila (Zn-Cam and Co-Cam) showed very different inhibitory properties with these compounds, as compared to the alpha-CA isozymes hCA I, II, and IX, and the beta-CA from Methanobacterium thermoautotrophicum (Cab). The best Zn-Cam inhibitors were sulfamic acid and acetazolamide, with inhibition constants in the range of 63-96 nM, whereas other investigated aromatic/heterocylic sulfonamides showed a rather levelled behavior, with K(1)s in the range of 0.12-1.70 muM. The best Co-Cam inhibitors were topiramate and p-aminoethyl-benzenesulfonamide, with K(1)s in the range of 0.12-0.13 muM, whereas the worst one was homosulfanilamide (K-1 of 8.50 muM). In the case of Cab, the inhibitory power of these compounds varied to a much larger extent, with sulfamic acid and sulfamide showing millimolar affinities (K(1)s in the range of 44-103 mM), whereas the best inhibitor was ethoxzolatnide, with a K-1 of 5.35 muM. Most of these sulfonamides showed inhibition constants in the range of 12-100 muM against Cab. Thus, the three CA families investigated up to now possess a very diverse affinity for sulfonamides, the inhibitors with important medicinal, and environmental applications. (C) 2004 Elsevier Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)6001-6006
Number of pages6
JournalBioorganic & Medicinal Chemistry Letters
Volume14
Issue number24
DOIs
Publication statusPublished - 20-Dec-2004
Externally publishedYes

Keywords

  • METHANOARCHAEON METHANOBACTERIUM-THERMOAUTOTROPHICUM
  • ISOZYME-IX
  • METHANOSARCINA-THERMOPHILA
  • CATALYTIC MECHANISM
  • ACTIVE-SITE
  • ANTICANCER
  • ISOENZYME
  • BINDING
  • DERIVATIVES
  • DESIGN

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