Chemical constituents from Cornus officinalis and their biological activity 1

Zhan-ying Ma, B. Yao, Liansheng Wang, Yang-qing He
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引用次数: 2

Abstract

Objective: To study the chemical constituents from Cornus officinalis Sieb., Et Zucc, and their peroxisome proliferator-activated receptors (PPARs) agonist activity. Materials and Methods: The leaves of C. officinalis were extracted three times with 90% EtOH at room temperature. The ethanol extracts were combined and concentrated under reduced pressure to yield residue, which was isolated and purified by silica gel and reverse-phase C 18 column chromatography. The structures were elucidated on the basis of spectroscopic evidence and their physiochemical characteristics. Cell-based luciferase reporter gene assays were used to evaluate PPARα/γ agonistic activities. Results: Five compounds were isolated and elucidated as 10-hydroxyhastatoside (1), β-dihydrocornin (2), isoquercitrin (3), loganin (4) and oleanolic acid (5). Conclusion: Compounds 1 and 2 were obtained from C. officinalis for the first time. Compound 3 exhibited moderate agonistic activities for PPARα, with EC 50 values of 29.5 μM.
山茱萸化学成分及其生物活性研究
目的:研究山茱萸的化学成分。以及它们的过氧化物酶体增殖物激活受体(PPARs)激动剂活性。材料与方法:用90%的乙醇水溶液在室温下提取三次山茱萸叶。将乙醇提取物组合减压浓缩得到残渣,用硅胶和反相c18柱层析分离纯化。根据光谱学证据和理化性质对其结构进行了鉴定。基于细胞的荧光素酶报告基因检测用于评估PPARα/γ的激动活性。结果:分离得到5个化合物,经鉴定为10-羟基草甘醇苷(1)、β-二氢角苷(2)、异槲皮苷(3)、马头草苷(4)和齐墩果酸(5)。结论:化合物1和2为首次从马头草中分离得到。化合物3对PPARα具有中等拮抗作用,ec50值为29.5 μM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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