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首页> 外文期刊>Natural product research >In vitro antiplasmodial and cytotoxic activities of sesquiterpene lactones from Vernonia fimbrillifera Less. (Asteraceae)
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In vitro antiplasmodial and cytotoxic activities of sesquiterpene lactones from Vernonia fimbrillifera Less. (Asteraceae)

机译:来自vernonia fimbrillifera的倍二萜内酯的体外抗蛋白酶和细胞毒性活性。 (Asteraceae)

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摘要

Due to the in vitro antiplasmodial activity of leaf extracts from Vernonia fimbrillifera Less. (Asteraceae), a bioactivity-guided fractionation was carried out. Three sesquiterpene lactones were isolated, namely 8-(4'-hydroxymethacrylate)-dehydromelitensin (1), onopordopicrin (2) and 8-[4'-hydroxymethacryloyloxy]-4-epi-sonchucarpolide (3). Their structures were elucidated by spectroscopic methods (1D and 2D NMR and MS analyses) and by comparison with published data. The isolated compounds exhibited antiplasmodial activity with IC50 values5g/mL. Cytotoxicity of the compounds against a human cancer cell line (HeLa) and a mouse lung epithelial cell line (MLE12) was assessed to determine selectivity. Compound 3 displayed promising selective antiplasmodial activity (SI10).
机译:由于vernonia fimbrillifera少的叶子提取物的体外抗溶剂活性。 (Asteraceae),进行生物活性引导的分馏。 分离了三个倍二萜内酯,即8-(4'-羟甲丙烯酸酯) - 丁二醇酯素(1),ONOOPORDOPICRIN(2)和8- [4'-羟甲基丙烯酰氧基] -4-EPI- SONCHUCARPOLINE(3)。 它们的结构通过光谱方法(1D和2D NMR和MS分析)和与已发表的数据进行阐明。 分离的化合物与IC50值5g / ml表现出抗癌活性。 评估对人癌细胞系(HELA)和小鼠肺上皮细胞系(MLE12)的化合物的细胞毒性以确定选择性。 化合物3显示有前途的选择性抗溶液活性(Si> 10)。

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