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来自意大利撒丁岛的特有物种阿里戈尼草中的双重HIV-1逆转录酶和整合酶抑制剂。

Dual HIV-1 reverse transcriptase and integrase inhibitors from Arrigoni, an endemic species of Sardinia (Italy).

作者信息

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

机构信息

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.

出版信息

Nat Prod Res. 2019 Jun;33(12):1798-1803. doi: 10.1080/14786419.2018.1434649. Epub 2018 Feb 4.

DOI:10.1080/14786419.2018.1434649
PMID:29397771
Abstract

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.

摘要

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。

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