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首页> 外文期刊>ChemMedChem >Design, Synthesis and Biological Evaluation of Trypanosoma brucei Trypanothione Synthetase Inhibitors
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Design, Synthesis and Biological Evaluation of Trypanosoma brucei Trypanothione Synthetase Inhibitors

机译:布鲁氏锥虫Trypanothione合成酶抑制剂的设计,合成及生物学评价

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摘要

Trypanothione synthetase (TryS) is essential for the survival of the protozoan parasite Trypanosoma brucei, which causes human African trypanosomiasis. It is one of only a handful of chemically validated targets for T. brucei in vivo. To identify novel inhibitors of TbTryS we screened our in-house diverse compound library that contains 62000 compounds. This resulted in the identification of six novel hit series of TbTryS inhibi- tors. Herein we describe the SAR exploration of these hit series, which gave rise to one common series with potency against the enzyme target. Cellular studies on these inhibitors confirmed on-target activity, and the compounds have proven to be very useful tools for further study of the trypanothione pathway in kinetoplastids.
机译:Trypanothione合成酶(TryS)对于原生动物寄生虫布氏锥虫(Trypanosoma brucei)的生存至关重要,而锥虫可引起人类非洲锥虫病。它是布鲁氏菌体内少数化学验证的靶标之一。为了鉴定TbTryS的新型抑制剂,我们筛选了包含62000种化合物的内部多样化化合物库。这样就鉴定出了六个新颖的TbTryS抑制剂系列。在这里,我们描述了这些命中序列的SAR探索,这产生了一个对酶标靶具有效力的常见序列。对这些抑制剂的细胞研究证实了靶向活性,并且该化合物已被证明是用于进一步研究运动质体中锥虫硫酮途径的非常有用的工具。

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