药效团
逆转录酶
四唑
对接(动物)
人类免疫缺陷病毒(HIV)
病毒学
化学
组合化学
生物
立体化学
医学
生物化学
核糖核酸
基因
护理部
作者
Peng Zhan,Zhenyu Li,Xinyong Liu,Erik De Clercq
标识
DOI:10.2174/138955709788681618
摘要
There is an urgent need for the design and development of new and safer drugs for the treatment of human immunodeficiency virus (HIV) infection, specifically active against drug-resistant viral strains. Recently, sulfanyltriazole/tetrazole derivatives were reported as potent HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs), with low nanomolar intrinsic activity against RT and submicromolar antiviral activity in HIV infected cells. In this review, the structural modifications, SAR analysis and docking studies of sulfanyltriazole/tetrazoles HIV-1 NNRTIs are discussed, and other interesting NNRTIs with the same or similar pharmacophore as the sulfanyltriazole/tetrazole derivatives are also presented and analyzed for their in SAR.
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