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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Arylazolylthioacetanilide. Part 8: Design, synthesis and biological evaluation of novel 2-(2-(2,4-dichlorophenyl)-2H-1,2,4-triazol-3-ylthio)-N-arylacetamides as potent HIV-1 inhibitors.
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Arylazolylthioacetanilide. Part 8: Design, synthesis and biological evaluation of novel 2-(2-(2,4-dichlorophenyl)-2H-1,2,4-triazol-3-ylthio)-N-arylacetamides as potent HIV-1 inhibitors.

机译:芳唑基硫代乙酰胺。第8部分:作为有效HIV-1抑制剂的新型2-(2-(2-(2,4-二氯苯基)-2H-1,2,4-三唑-3-基硫基)-N-芳基乙酰胺的设计,合成和生物学评估。

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摘要

The development of novel HIV-1 NNRTIs offers the possibility of generating novel structures with increased potency. Based on the bioisosteric principle, a novel series of 2-(2-(2,4-dichlorophenyl)-2H-1,2,4-triazol-3-ylthio)-N-arylacetamide derivatives were designed, synthesized using a simple and efficient synthetic route, structurally confirmed by spectral analysis, evaluated for their anti-HIV activity in MT-4 cells and their inhibitory effect on HIV-1 RT. The results showed that some of the new compounds displayed low micromolar potency for inhibiting HIV-1 replication and promising activities against several selected resistant strains that confer resistance to current NNRTIs. However, all newly synthesized derivatives were not active against HIV-2 replication.
机译:新型HIV-1 NNRTIs的开发提供了产生具有增强效价的新型结构的可能性。基于生物立体异构原理,设计了一系列新颖的2-(2-(2,4-二氯苯基)-2H-1,2,4-三唑-3-基硫基)-N-芳基乙酰胺衍生物,使用简单的方法合成通过光谱分析在结构上证实有效的合成路线,评估了它们在MT-4细胞中的抗HIV活性及其对HIV-1 RT的抑制作用。结果表明,一些新化合物显示出低的抑制HIV-1复制的微摩尔效价,并且对一些赋予当前NNRTI耐药性的耐药菌株具有良好的活性。但是,所有新合成的衍生物都没有抗HIV-2复制的活性。

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