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美拉唑及其生物电子等排体4H-1,2,4-三唑:比较杀锥虫、细胞毒性和遗传毒性活性及其与布氏锥虫硝基还原酶的体外和计算机模拟相互作用。

Megazol and its bioisostere 4H-1,2,4-triazole: comparing the trypanocidal, cytotoxic and genotoxic activities and their in vitro and in silico interactions with the Trypanosoma brucei nitroreductase enzyme.

作者信息

Carvalho Alcione Silva de, Salomão Kelly, Castro Solange Lisboa de, Conde Taline Ramos, Zamith Helena Pereira da Silva, Caffarena Ernesto Raúl, Hall Belinda Suzette, Wilkinson Shane Robert, Boechat Núbia

机构信息

Departamento de Síntese de Fármacos, Farmanguinhos, Fiocruz, Rio de Janeiro, RJ, Brasil.

Laboratório de Biologia Celular, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro, RJ, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 2014 Jun;109(3):315-23. doi: 10.1590/0074-0276140497. Epub 2014 Mar 18.

Abstract

Megazol (7) is a 5-nitroimidazole that is highly active against Trypanosoma cruzi and Trypanosoma brucei, as well as drug-resistant forms of trypanosomiasis. Compound 7 is not used clinically due to its mutagenic and genotoxic properties, but has been largely used as a lead compound. Here, we compared the activity of 7 with its 4H-1,2,4-triazole bioisostere (8) in bloodstream forms of T. brucei and T. cruzi and evaluated their activation by T. brucei type I nitroreductase (TbNTR) enzyme. We also analysed the cytotoxic and genotoxic effects of these compounds in whole human blood using Comet and fluorescein diacetate/ethidium bromide assays. Although the only difference between 7 and 8 is the substitution of sulphur (in the thiadiazole in 7) for nitrogen (in the triazole in 8), the results indicated that 8 had poorer antiparasitic activity than 7 and was not genotoxic, whereas 7 presented this effect. The determination of Vmax indicated that although 8 was metabolised more rapidly than 7, it bounds to the TbNTR with better affinity, resulting in equivalent kcat/KM values. Docking assays of 7 and 8 performed within the active site of a homology model of the TbNTR indicating that 8 had greater affinity than 7.

摘要

美唑(7)是一种5-硝基咪唑,对克氏锥虫和布氏锥虫以及耐药形式的锥虫病具有高度活性。化合物7因其致突变和基因毒性特性未在临床上使用,但已被广泛用作先导化合物。在此,我们比较了7与其4H-1,2,4-三唑生物电子等排体(8)对布氏锥虫和克氏锥虫血流形式的活性,并评估了它们被布氏锥虫I型硝基还原酶(TbNTR)激活的情况。我们还使用彗星试验和荧光素二乙酸酯/溴化乙锭试验分析了这些化合物在全血中的细胞毒性和基因毒性作用。尽管7和8之间的唯一区别是硫(在7中的噻二唑中)被氮(在8中的三唑中)取代,但结果表明8的抗寄生虫活性比7差,且没有基因毒性,而7有此效应。Vmax的测定表明,尽管8比7代谢更快,但它与TbNTR的结合亲和力更好,导致kcat/KM值相当。在TbNTR同源模型的活性位点内对7和8进行的对接试验表明,8比7具有更高的亲和力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c3e/4131783/ab4458c60d39/0074-0276-mioc-109-03-00315-gf01.jpg

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