首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Semisynthesis of α-methyl-γ-lactones and in vitro evaluation of their activity on protein farnesyltransferase
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Semisynthesis of α-methyl-γ-lactones and in vitro evaluation of their activity on protein farnesyltransferase

机译:α-甲基-γ-内酯的半合成及其对蛋白质法呢基转移酶活性的体外评价

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摘要

The semisynthesis of xanthanolide derivatives is reported from xanthinin and 4-epi-isoxanthanol, two sesquiterpene lactones isolated from the crude chloroformic extract of the leaves of Xanthium macrocarpum DC. (Asteraceae) by liquid/liquid chromatography. In vitro evaluation of their protein farnesyltransferase (PFTase) inhibitory activity has been investigated. In contrast to other biological activities of xanthanolides, PFTase inhibition is not associated with the presence of the potentially toxic α-methylene- γ-lactone function.
机译:黄嘌呤衍生物的半合成是从黄嘌呤和4-表-异黄嘌呤中报道的,这是从大黄椒DC的叶的粗制氯仿提取物中分离得到的两种倍半萜烯内酯。 (菊科)通过液/液色谱法。已经研究了对其蛋白法呢基转移酶(PFTase)抑制活性的体外评估。与黄嘌呤类内酯的其他生物活性相反,PFTase抑制与潜在毒性的α-亚甲基-γ-内酯功能的存在无关。

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