Sulfonamide inhibition studies of the β carbonic anhydrase from Drosophila melanogaster

被引:11
作者
Syrjanen, Leo [1 ,2 ]
Parkkila, Seppo [1 ,2 ,3 ,4 ]
Scozzafava, Andrea [5 ]
Supuran, Claudiu T. [5 ,6 ]
机构
[1] Univ Tampere, Sch Med, FIN-33101 Tampere, Finland
[2] Univ Tampere, BioMediTech, FIN-33101 Tampere, Finland
[3] Fimlab Labs Ltd, Tampere, Finland
[4] Tampere Univ Hosp, Tampere, Finland
[5] Univ Florence, Dipartimento Chim, Lab Chim Bioinorgan, I-50019 Florence, Italy
[6] Univ Florence, Neurofarba Dipartment, Sez Sci Farmaceut & Nutraceut, I-50019 Florence, Italy
基金
芬兰科学院;
关键词
Carbonic anhydrase; beta-Class enzyme; Drosophila melanogaster; Sulfonamide; Enzyme inhibitor; YEAST SACCHAROMYCES-CEREVISIAE; PATHOGENS CANDIDA-ALBICANS; CRYPTOCOCCUS-NEOFORMANS; CLASS ENZYME; GAMMA-CLASS; AROMATIC/HETEROCYCLIC SULFONAMIDES; CLONING; MECHANISM; BINDING; IDENTIFICATION;
D O I
10.1016/j.bmcl.2014.04.117
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An inibition study of the beta-carbonic anhydrase (CA, EC 4.2.1.1) DmBCA from the insect Drosophila melanogaster with sulfonamides and sulfamates is reported. Among the panel of 40 investigated compounds, the best DmBCA inhibitors were the sulfonylated benzenesulfonamides and ethoxzolamide, which showed inhibition constants in the range of 65.3-138 nM. Methazolamide and sulthiame were also effective inhibitors with K(I)s ranging between 237 and 249 nM, whereas most of the simple aromatic/heterocyclic sulfonamides showed inhibition constants in the range of 0.47-6.40 mu M. Topiramate, zonisamide and saccharine did not inhibit DmBCA. As orthologs of this mitochondrial CA are found in many insect species involved in the spread of various diseases, inhibitors interfering with their activity may be of interest for developing insecticides with an alternative mechanism of action to the presently used agents, for which many insects developed extensive resistance. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2797 / 2801
页数:5
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