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首页> 外文期刊>Parasitology Research >Antiplasmodial activity of novel stilbene derivatives isolated from Parthenocissus tricuspidata from South Korea.
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Antiplasmodial activity of novel stilbene derivatives isolated from Parthenocissus tricuspidata from South Korea.

机译:从韩国爬山虎中分离出的新型二苯乙烯衍生物的抗血浆活性。

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摘要

New stilbene glycoside, piceid-(1-->6)-beta-D: -glucopyranoside (compound 2, Fig. 1), was isolated from the MeOH extract of the leaves of Parthenocissus tricuspidata (Vitaceae) together with four known compounds, piceid (compound 1, Fig. 1), resveratrol (compound 3, Fig. 1), longistylin A (compound 4, Fig. 1), and longistylin C (compound 5, Fig. 1). Their structures were determined spectroscopically, particularly by 2D nuclear magnetic resonance (NMR) spectroscopic and chemical analysis. The antiplasmodial activity of isolated compounds were determined in vitro against a chloroquine-sensitive strain of Plasmodium falciparum (D10). Among the compounds isolated, piceid-(1-->6)-beta-D: -glucopyranoside (2) had the most potential inhibition, with inhibitory concentration (IC(50)) values of 5.3 muM. To our knowledge, antiplasmodial activity of functional group position of stilbene is now being reported for the first time in this study. The result shows that the 3, 4'-position in stilbenes might play an essential role in antiplasmodial activity.
机译:从三叶爬山虎(Vitaceae)的MeOH提取物中分离出新的1,2-二苯乙烯苷,piceid-(1-> 6)-beta-D:-glucopyranoside(化合物2,图1),以及四种已知化合物,皮塞啶(化合物1,图1),白藜芦醇(化合物3,图1),longistylin A(化合物4,图1)和longistylin C(化合物5,图1)。它们的结构是通过光谱确定的,特别是通过2D核磁共振(NMR)光谱和化学分析确定的。在体外确定分离的化合物对恶性疟原虫(D10)的氯喹敏感菌株的抗血浆活性。在分离的化合物中,piceid-(1-> 6)-beta-D:-吡喃葡萄糖苷(2)具有最大的抑制潜力,抑制浓度(IC(50))值为5.3μM。据我们所知,这项研究中首次报道了的官能团位置的抗血浆活性。结果表明,斯蒂芬类药物的3,4'-位可能在抗疟原虫活性中起重要作用。

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