Campiani Giuseppe, Ramunno Anna, Maga Giovanni, Nacci Vito, Fattorusso Caterina, Catalanotti Bruno, Morelli Elena, Novellino Ettore
Dipartimento Farmaco Chimico Tecnologico, Universitá degli Studi di Siena, via Aldo Moro, 53100 Siena, Italy.
Curr Pharm Des. 2002;8(8):615-57. doi: 10.2174/1381612024607207.
Along with nucleoside reverse transcriptase inhibitors (NRTIs) and protease inhibitors (PIs), non-nucleoside reverse transcriptase inhibitors (NNRTIs) have gained a definitive and important place in the treatment of HIV-1 infections, and are in rapid development. These compounds can be grouped into two classes: the first generation NNRTIs, mainly discovered by random screening, and the second generation NNRTIs, developed as a result of comprehensive strategies involving molecular modelling, rationale-based drug synthesis, biological and pharmacokinetic evaluations. The recent boom of NNRTIs is mainly due to their antiviral potency, high specificity and low toxicity. The rapid emergence of drug-resistant HIV-1 strains induced by the first generation drugs is a disadvantage bypassed, in part, by the broad spectrum second generation NNRTIs. Starting from the first generation, this review will focus on the second generation NNRTIs dealing with the recent and most interesting published results, highlighting the guidelines for the development of a third generation of NNRTIs.
与核苷类逆转录酶抑制剂(NRTIs)和蛋白酶抑制剂(PIs)一样,非核苷类逆转录酶抑制剂(NNRTIs)在HIV-1感染治疗中已占据了明确且重要的地位,并且仍在快速发展。这些化合物可分为两类:第一代NNRTIs,主要通过随机筛选发现;以及第二代NNRTIs,是通过涉及分子建模、基于理论的药物合成、生物学和药代动力学评估的综合策略开发而来。NNRTIs最近的蓬勃发展主要归因于其抗病毒效力、高特异性和低毒性。第一代药物诱导产生的耐药HIV-1毒株的迅速出现是一个缺点,而第二代广谱NNRTIs在一定程度上克服了这一缺点。从第一代开始,本综述将聚焦于第二代NNRTIs,探讨近期最有趣的已发表结果,突出第三代NNRTIs的开发指南。