Sanna Cinzia, Rigano Daniela, Corona Angela, Piano Dario, Formisano Carmen, Farci Domenica, Franzini Genni, Ballero Mauro, Chianese Giuseppina, Tramontano Enzo, Taglialatela-Scafati Orazio, Esposito Francesca
a Department of Life and Environmental Sciences , University of Cagliari , Cagliari , Italy.
b Department of Pharmacy, School of Medicine and Surgery , University of Naples Federico II , Naples , Italy.
Nat Prod Res. 2019 Jun;33(12):1798-1803. doi: 10.1080/14786419.2018.1434649. Epub 2018 Feb 4.
During our search for potential templates of HIV-1 reverse transcriptase (RT) and integrase (IN) dual inhibitors, the methanolic extract obtained from aerial parts of was investigated. Repeated bioassay-guided chromatographic purifications led to the isolation of the following secondary metabolites: myricetin, myricetin 3--rutinoside, myricetin-3--(6″--galloyl)-β-d-galactopyranoside, (-)-epigallocatechin 3--gallate, tryptamine, ferulic and phloretic acids. The isolated compounds were tested on both HIV-1 RT-associated RNase H and IN activities. Interestingly, (-)-epigallocatechin-3--gallate and myricetin-3--(6″--galloyl)-β-d-galactopyranoside potently inhibited both enzyme activities with IC values ranging from 0.21 to 10.9 μM. Differently, tryptamine and ferulic acid exhibited a significant inhibition only on the IN strand transfer reaction, showing a selectivity for this viral enzyme. Taken together these results strongly support the potential of this plant as a valuable anti HIV-1 drugs source worthy of further investigations.
在我们寻找HIV-1逆转录酶(RT)和整合酶(IN)双重抑制剂的潜在模板的过程中,对从[植物名称]地上部分获得的甲醇提取物进行了研究。通过反复的生物测定指导的色谱纯化,分离出以下次生代谢产物:杨梅素、杨梅素3 - 芸香糖苷、杨梅素-3 - (6″ - 没食子酰基)-β - D - 吡喃半乳糖苷、(-)-表没食子儿茶素3 - 没食子酸酯、色胺、阿魏酸和根皮酸。对分离出的化合物进行了HIV-1 RT相关核糖核酸酶H和IN活性测试。有趣的是,(-)-表没食子儿茶素3 - 没食子酸酯和杨梅素-3 - (6″ - 没食子酰基)-β - D - 吡喃半乳糖苷能有效抑制这两种酶的活性,IC值范围为0.21至10.9 μM。不同的是,色胺和阿魏酸仅对IN链转移反应表现出显著抑制,显示出对这种病毒酶的选择性。综合这些结果有力地支持了这种植物作为有价值的抗HIV-1药物来源的潜力,值得进一步研究。