乙酰胺
三唑
异丙基
EC50型
人类免疫缺陷病毒(HIV)
化学
立体化学
逆转录酶
1,2,3-三唑
1,2,4-三唑
组合化学
核苷逆转录酶抑制剂
体外
病毒学
生物
生物化学
有机化学
核糖核酸
基因
作者
Zhenyu Li,Yuan Cao,Peng Zhan,Christophe Pannecouque,Jan Balzarini,Erik De Clercq,Yuemao Shen,Xinyong Liu
出处
期刊:Medicinal Chemistry
[Bentham Science Publishers]
日期:2013-08-01
卷期号:9 (7): 968-973
被引量:9
标识
DOI:10.2174/1573406411309070010
摘要
A series of novel 1,2,4-triazole thioacetanilide derivatives has been designed, synthesized and evaluated for their anti-HIV activities in MT-4 cells. Half of these compounds showed moderate to potent activities against wild-type HIV-1 with an EC50 ranging from 38.0 μM to 4.08 µM. Among them, 2-(4-(2-fluorobenzyl)-5-isopropyl-4H-1,2,4-triazol- 3-ylthio)-N-(2-nitrophenyl)acetamide 7d was identified as the most promising compound (EC50 = 4.26 µM, SI = 49). However, no compound was active against HIV-2. The preliminary structure-activity relationships among the newly synthesized congeners are discussed. Keywords: HIV-1, AIDS, NNRTIs, 1, 2, 4-triazole thioacetanilides, Anti-HIV-1 activity.
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