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A novel icariin type flavonoid from Epimedium pseudowushanense

机译:来自淫羊藿的新型icariin类型黄酮类化合物

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A novel icariin type flavonoid glycoside with a malonaldehydic acid intramolecular ester and two known flavonoid glycosides were isolated from Epimedium pseudowushanense. Their structures were elucidated on the basis of spectroscopic analysis and comparison of their data to the values reported in the literatures. The anti-inflammatory activities of these compounds icariin 3′′′-O-malonaldehydic acid intramolecular 1′′′′, 2′′′ ester (1), icariin (2) and epimedin C (3) were tested. The results indicated that compounds 1, 2 and 3 showed maximal inhibitory ratio of 27.91, 44.80 and 46.61%, respectively in in vitro anti-inflammatory activity on LPS-induced TNF-α secretion in RAW264.7 cells. Compounds icariin (2) and epimedin C (3) were found to inhibit the secretion of TNF-α to a comparable degree as quercetin.
机译:用淫羊藿柱柱柱分离出一种新的icariin型黄酮类黄酮糖苷和两种已知的黄酮糖苷分离出两种已知的黄酮糖苷。 它们的结构在光谱分析和与文献报告的价值观的基础上阐明了它们的数据。 测试这些化合物的抗炎活性icariin 3'' - o-苯甲酸分子内酸分子内1''',2''酯(1),icariin(2)和表咪啶c(3)。 结果表明,化合物1,2和3显示出在RAW264.7细胞中LPS诱导的TNF-α分泌的体外抗炎活性中的最大抑制比例为27.91,44.80和46.61%。 发现化合物icariin(2)和脱像蛋白C(3)抑制TNF-α的分泌到与槲皮素相当的程度。

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