Carbonic Anhydrase Inhibitors. Part 55 1 Metal Complexes of 1,3,4-Thiadiazole-2-Sulfonamide Derivatives: In Vitro Inhibition Studies With Carbonic Anhydrase Isozymes I, II and IV
Author(s) -
Claudiu T. Supuran,
Andrea Scozzafava,
Fabrizio Briganti,
Marc A. Ilies,
Andrei Jitianu
Publication year - 1998
Publication title -
metal-based drugs
Language(s) - English
Resource type - Journals
ISSN - 0793-0291
DOI - 10.1155/mbd.1998.103
Subject(s) - carbonic anhydrase , isozyme , chemistry , electron paramagnetic resonance , thermogravimetric analysis , metal , enzyme , physics , biochemistry , nuclear magnetic resonance , organic chemistry
Coordination compounds of 5-chloroacetamido-1,3,4-thiadiazole-2-sulfonamide (Hcaz) with V(IV), Cr(lll), Fe(ll), Co(ll), Ni(ll) and Cu(ll) have been prepared and characterized by standard procedures (spectroscopic, magnetic, EPR, thermogravimetric and conductimetric measurements). Some of these compounds showed very good in vitro inhibitory properties against three physiologically relevant carbonic anhydrase (CA)isozymes, i.e., CA I, II, and IV. The differences between these isozymes in susceptibility to inhibition by these metal complexes is discussed in relationship to the characteristic features of their active sites, and is rationalized in terms useful for developing isozyme-specific CA inhibitors.
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