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Inhibitors of Tick-Borne Flavivirus Reproduction from Structure-Based Virtual Screening

机译:基于结构的虚拟筛选的of虫黄病毒复制的抑制剂

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Flaviviruses form a large family of enveloped viruses affecting millions of people over the world. To date, no specific therapy was suggested for the infected people, making the treatment exclusively symptomatic. Several attempts were performed earlier for the design of fusion inhibitors for mosquito-borne flaviviruses, whereas for the tick-borne flaviviruses such design had not been performed. We have constructed homology models of envelope glycoproteins of tick-transmitted flaviviruses with the detergent binding pocket in the open state. Molecular docking of substituted 1,4-dihydropyridines and pyrido[2,1-b][1,3,5]-thiadiazines was made against these models, and 89 hits were selected for the in vitro experimental evaluation. Seventeen compounds showed significant inhibition against tick-borne encephalitis virus, Powassan virus, or Omsk hemorrhagic fever virus in the 50% plaque reduction test in PEK cells. These compounds identified through rational design are the first ones possessing reproduction inhibition activity against tick-borne flaviviruses.
机译:黄病毒是构成包膜病毒的一大家族,影响着全球数百万人。迄今为止,没有建议对感染者进行特异性治疗,这使得该治疗仅是对症治疗。较早地进行了几次尝试来设计蚊传黄病毒的融合抑制剂,而对于for传黄病毒则没有进行这种设计。我们已经建立了去污剂结合口袋处于打开状态的tick传播黄病毒包膜糖蛋白的同源模型。针对这些模型,将取代的1,4-二氢吡啶和吡啶并[2,1-b] [1,3,5]-噻二嗪进行分子对接,选择了89个命中物进行体外实验评估。在PEK细胞的50%噬斑减少试验中,十七种化合物对tick传脑炎病毒,波瓦桑病毒或鄂木斯克出血热病毒显示出显着抑制作用。通过合理设计确定的这些化合物是第一个对tick传黄病毒具有抑制繁殖活性的化合物。

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