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alpha-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。

Semisynthesis of alpha-methyl-gamma-lactones and in vitro evaluation of their activity on protein farnesyltransferase.

机构信息

IFR 149 QUASAV, Laboratoire SONAS, UFR des Sciences Pharmaceutiques et Ingénierie de la Santé, Angers, France.

出版信息

J Enzyme Inhib Med Chem. 2010 Apr;25(2):172-9. doi: 10.3109/14756360903169592.

Abstract

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 alpha-methylene-gamma-lactone function.

摘要

报道了从黄桐叶中的黄桐宁和 4-表异莪术呋喃二烯醇两种倍半萜内酯,通过液/液色谱法从粗氯仿提取物中分离出来,然后对它们的法呢基转移酶(PFTase)抑制活性进行了体外评价。与黄桐醇的其他生物活性不同,PFTase 抑制作用与潜在毒性的α-亚甲基-γ-内酯功能无关。

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