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计算机辅助药物重定位在寻找新型克氏锥虫蛋白酶抑制剂中的应用:发现胺碘酮和溴隐亭的抑制作用。

Application of computer-aided drug repurposing in the search of new cruzipain inhibitors: discovery of amiodarone and bromocriptine inhibitory effects.

机构信息

Medicinal Chemistry, Department of Biological Sciences, Faculty of Exact Sciences, National University of La Plata , 47 y 115, La Plata (B1900AJI), Buenos Aires, Argentina.

出版信息

J Chem Inf Model. 2013 Sep 23;53(9):2402-8. doi: 10.1021/ci400284v. Epub 2013 Aug 16.

DOI:10.1021/ci400284v
PMID:23906322
Abstract

Cruzipain (Cz) is the major cystein protease of the protozoan Trypanosoma cruzi , etiological agent of Chagas disease. From a 163 compound data set, a 2D-classifier capable of identifying Cz inhibitors was obtained and applied in a virtual screening campaign on the DrugBank database, which compiles FDA-approved and investigational drugs. Fifty-four approved drugs were selected as candidates, four of which were acquired and tested on Cz and T. cruzi epimastigotes. Among them, the antiparkinsonian and antidiabetic drug bromocriptine and the antiarrhythmic amiodarone showed dose-dependent inhibition of Cz and antiproliferative activity on the parasite.

摘要

克氏锥虫 cruzipain (Cz) 是原生动物克氏锥虫的主要半胱氨酸蛋白酶,也是恰加斯病的病原体。从一个包含 163 种化合物的数据集出发,我们获得了一个能够识别 Cz 抑制剂的 2D 分类器,并将其应用于 DrugBank 数据库(包含美国食品和药物管理局批准和正在研究的药物)的虚拟筛选活动中。从数据库中选择了 54 种已批准的药物作为候选药物,其中 4 种药物被购买并用于检测克氏锥虫 cruzipain (Cz) 和锥虫的棘阿米巴原虫。其中,抗帕金森病和抗糖尿病药物溴隐亭和抗心律失常药物胺碘酮对 Cz 表现出剂量依赖性抑制作用,并且对寄生虫也具有抗增殖活性。

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