Kang Dongwei, Song Yu'ning, Chen Wenmin, Zhan Peng, Liu Xinyong
Department of Medicinal Chemistry, Key laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Shandong University, 44, West Culture Road, 250012, Jinan, Shandong, P. R. China.
Mol Biosyst. 2014 Aug;10(8):1998-2022. doi: 10.1039/c4mb00147h.
HIV-1 reverse transcriptase, protease and integrase have been recognized as clinically validated but still underexploited targets for antiretroviral treatment. Although a large number of inhibitors have been used in clinical trials, the rapid emergence of multiple drug-resistant strains requires the identification of not only novel classes of antiretroviral drugs that act via the unprecedented mechanism of action but also innovative drug discovery strategies towards these three important targets. This review summarizes and discusses current endeavours towards the discovery and development of novel inhibitors with alternative mechanisms of action, and also provides examples illustrating new methodologies in medicinal chemistry that contribute to the identification of novel antiretroviral agents.
HIV-1逆转录酶、蛋白酶和整合酶已被公认为抗逆转录病毒治疗中经过临床验证但仍未得到充分利用的靶点。尽管大量抑制剂已用于临床试验,但多重耐药菌株的迅速出现不仅需要鉴定通过前所未有的作用机制发挥作用的新型抗逆转录病毒药物类别,还需要针对这三个重要靶点的创新药物发现策略。本综述总结并讨论了目前在发现和开发具有替代作用机制的新型抑制剂方面所做的努力,还提供了一些例子来说明药物化学中的新方法,这些方法有助于鉴定新型抗逆转录病毒药物。