首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Inhibition of MRP1 transport activity by phenolic and terpenic compounds isolated from Euphorbia species.
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Inhibition of MRP1 transport activity by phenolic and terpenic compounds isolated from Euphorbia species.

机译:酚类和三萜化合物从大戟属物种中分离的酚类和三萜化合物抑制MRP1运输活性。

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摘要

BACKGROUND: A search for inhibitors of multidrug resistance (MDR)-associated protein 1 (MRP1) was performed among the compounds isolated from Euphorbia species, plants traditionally used in folk medicine. MATERIALS AND METHODS: Fifteen compounds with terpenic or phenolic structures (macrocyclic and polycyclic diterpenes, coumarins, stilbenes and flavonoids) were isolated from the methanol extracts of Euphorbia lagascae and Euphorbia tuckeyana or obtained by derivatization. A functional test based on measuring the efflux of fluorescent MRP1 substrate (BCECF) from human erythrocytes was employed. RESULTS: Effective MRP1 inhibitors were identified among the stilbenes (piceatannol and its derivatives) and the flavonoids (aromadendrin, naringenin and its derivatives). CONCLUSION: Euphorbia species constitute a promising source of multidrug resistance modulators.
机译:背景技术:在从大戟属物种中分离的化合物中进行多药抗性(MDR)抗性(MDR)抑制剂(MRP1)的搜索,传统上用于民间医学的植物。 材料和方法:从大戟属荔枝醇和大戟和大戟属Tuckeyana的甲醇提取物中分离出萜烯或酚醛结构的十五种化合物(酚醛结构,香豆素,斯蒂芬,香豆素,斯蒂芬和黄酮类化合物)或通过衍生化获得。 采用基于测量人红细胞的荧光MRP1底物(BCECF)的荧光MRP1基材(BCECF)的功能试验。 结果:斯蒂芬(Piceatannol及其衍生物)和黄酮类化合物(芳香丹丁林,柚子及其衍生物)中鉴定了有效的MRP1抑制剂。 结论:大戟属物种构成了多药抗性调制器的有希望的来源。

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