逆转录酶
人类免疫缺陷病毒(HIV)
核苷逆转录酶抑制剂
逆转录酶抑制剂
胺气处理
病毒学
核苷类似物
核苷
立体化学
化学
奈韦拉平
医学
西达
核糖核酸
病毒性疾病
抗逆转录病毒疗法
生物化学
有机化学
病毒载量
基因
作者
Megan A. Young,Thomas R. Lane,Renuka Raman,Julie A. Nelson,Olga Riabova,Elena Kazakova,Natalia Monakhova,Andrey Tsedilin,Steven D. Rees,Daniel Quinnell,Vadim Makarov,Geoffrey Chang,Sean Ekins
标识
DOI:10.1021/acsinfecdis.5c00189
摘要
The use of highly active antiretroviral therapy (HAART) has made the human immunodeficiency virus (HIV) a chronic disease rather than a terminal disease. Non-nucleoside reverse transcriptase inhibitors (NNRTIs) are an important component of HAART, although we are seeing clinically relevant drug-resistant mutants such that there is a need to develop new molecules. We recently identified a new class of N-phenyl-1-(phenylsulfonyl)-1H-1,2,4-triazol-3-amine HIV-1 NNRTI, with one known as compound 12126065, with sub nanomolar (nM) potency in TZM-bl cells (HeLa cells expressing CD4, CCR5, and CXCR4) with no in vivo acute or subacute toxicity. We now describe the cryo-EM structure of this molecule (resolution of 3.53 Å) and compare it to analogues and other known NNRTIs. We also describe the synthesis and activity of five additional analogues of this class of compounds, some of which have promising activity against a K103N/Y181C (A17) double mutant, which will enable the design of future molecules.
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