Carbonic anhydrase inhibitors. Metal complexes of 5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide with topical intraocular pressure lowering properties: The influence of metal ions upon the pharmacological activity

被引:17
作者
Briganti, F
Tilli, S
Mincione, G
Mincione, F
Menabuoni, L
Supuran, CT
机构
[1] Univ Florence, Lab Chim Inorgan & Bioinorgan, I-50121 Florence, Italy
[2] Univ Florence, Inst Ophthalmol, I-50134 Florence, Italy
[3] Osped Giovanni Dio, SO Oculist, I-50123 Florence, Italy
来源
JOURNAL OF ENZYME INHIBITION | 2000年 / 15卷 / 02期
关键词
topical sulfonamide; chlorazolamide; carbonic anhydrase; metal complex; intraocular pressure lowering; antiglaucoma drug;
D O I
10.1080/14756360009030350
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metal complexes of a sulfonamide possessing strong carbonic anhydrase (CA) inhibitory properties, 5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide (chlorazolamide) have been obtained from the sodium salt of the sulfonamide and the following metal ions: Mg(II), Zn(II), Mn(II), Cu(II), Co(II), Ni(II), Be(II), Cd(II), Pb(II), Al(III), Fe(III) and La(III). The original sulfonamide and its complexes were assayed for the in vitro inhibition of three CA isozymes, CA I, II, and IV, some of which play a critical role in ocular fluid secretion. All these compounds (the sulfonamide and its metal complexes) behaved as powerful inhibitors against the three investigated isozymes. The parent sulfonamide possessed an extremely weak topical pressure lowering effect when administered as a 1-2% suspension into the rabbit eye, but some of its metal complexes, such as the Mg(II), Zn(II), Mn(II) and Cu(II) derivatives, lower intraocular pressure (IOP) in experimental animals very well. Ex vivo data showed a 99.5-99.9% CA II inhibition in ocular fluids and tissues of rabbits treated with these agents, proving that the observed IOP lowering is due to CA inhibition. The influence of the different metal ions upon the efficiency of the obtained complexes as pressure lowering drugs are discussed, leading to the possibility of designing more selective/potent pharmacological agents from this class.
引用
收藏
页码:185 / 200
页数:16
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