逆转录酶
人类免疫缺陷病毒(HIV)
立体化学
分子模型
核苷
化学
核苷逆转录酶抑制剂
核苷酸转移酶
组合化学
计算生物学
病毒学
生物
生物化学
核糖核酸
基因
作者
Ye Tian,Peng Zhan,Diwakar Rai,Jiyan Zhang,Erik De Clercq,Xinyong Liu
标识
DOI:10.2174/092986712800167383
摘要
Derived from the structure of 1H,3H-thiazolo[3,4-a]benzimidazoles (TBZs), 2,3-diaryl-1,3-thiazolidin-4-one derivatives became a novel class of HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs). Under the guidance of continuous structureactivity relationship (SAR) analysis and molecular modeling, various structural modifications were carried out on nearly all the positions of the thiazolidin-4-one nucleus. Some of the derivatives proved to be highly effective against HIV-1 replication at 10–40 nanomolar concentration ranges with minimal cytotoxicities. In this article, the whole development of 2,3-diaryl-1,3-thiazolidin-4-one series from the discoveries to recent advances, their panoramic SAR studies and binding modes based on molecular modeling were reviewed, and also some enlightenments for further investigation were presented. Keywords: HIV, AIDS, 1, 3-Thiazolidin-4-ones, HIV-1 NNRTIs, Antiviral, Drug design
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