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新型含氟二氮杂卓并嘧啶衍生物作为强效HIV-1非核苷类逆转录酶抑制剂:WO2014072419专利评估

Novel fluorine-containing DAPY derivatives as potent HIV-1 NNRTIs: a patent evaluation of WO2014072419.

作者信息

Meng Qing, Liu Na, Huang Boshi, Zhan Peng, Liu Xinyong

机构信息

a Shandong University, School of Pharmaceutical Sciences, Key Laboratory of Chemical Biology (Ministry of Education), Department of Medicinal Chemistry , 44, West Culture Road, 250012, Jinan, Shandong, P. R. China

出版信息

Expert Opin Ther Pat. 2015;25(12):1477-86. doi: 10.1517/13543776.2016.1088832. Epub 2015 Sep 28.

Abstract

Diarylpyrimidine (DAPY) derivatives, one family of HIV non-nucleoside reverse transcriptase (RT) inhibitors (NNRTIs) with superior activities against wild-type (WT) HIV-1 and NNRTI-resistant strains, have attracted much attention in the past decade. A series of DAPY derivatives featuring a fluorine atom on the central ring were reported as novel NNRTIs in the patent WO2014072419. Some compounds exhibited robust potency against both WT and mutant strains, which were approximately equal to or higher than those of the reference drug TMC120. Moreover, it has become evident that fluorinated molecules have a remarkable record in many other potent NNRTIs. Thus, this survey provides a sampling of renowned fluorinated NNRTIs and their mode of action, with an analysis clarifying the functional roles and impact of fluorine substitution on antiviral potency. We envision that fluorinated NNRTIs will play a continuing role in affording anti-HIV drug candidates for therapeutic applications.

摘要

二芳基嘧啶(DAPY)衍生物是一类HIV非核苷逆转录酶(RT)抑制剂(NNRTIs),对野生型(WT)HIV-1和耐NNRTI毒株具有优异活性,在过去十年中备受关注。专利WO2014072419报道了一系列在中心环上带有氟原子的DAPY衍生物作为新型NNRTIs。一些化合物对野生型和突变株均表现出强大的效力,与参考药物TMC120相当或更高。此外,很明显氟化分子在许多其他强效NNRTIs中也有显著表现。因此,本综述提供了著名的氟化NNRTIs及其作用模式的样本,并通过分析阐明氟取代对抗病毒效力的功能作用和影响。我们设想氟化NNRTIs将在为治疗应用提供抗HIV候选药物方面继续发挥作用。

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