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Anti-platelet effects of flavonoids and flavonoid-glycosides from Sophora japonica.

机译:槐花中总黄酮和总黄酮苷的抗血小板作用。

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摘要

A methanol extract of Sophora japonica was subjected to anti-platelet activity guided fractionation affording the isolation of four flavonoids and six flavonoid-glycosides: biochanin A (1), irisolidone (2), genistein (3), sissotrin (4), sophorabioside (5), genistin (6), tectoridin (7), apigenin (8), quercitrin (9), and rutin (10). The structure of each compound was determined by a variety of spectroscopic methods. Among the compounds, 1, 3, and 7 showed approximately 2.5-6.5 fold greater inhibitory effects on arachidonic acid (AA) and U46619 induced platelet aggregation (IC50: 19.9 and 99.8 microM; 20.3 and 53.8 microM; 25.9 and 123.4 microM, respectively) than acetylsalicylic acid (ASA, IC50: 63.0 and 350.0 microM). Compound 2 was an approximately 22-40 fold stronger inhibitor than ASA on AA and U46619 induced aggregation (IC50: 1.6 and 15.6 microM, respectively).
机译:对槐花的甲醇提取物进行抗血小板活性引导分级分离,从而分离出四种黄酮和六种类黄酮糖苷:生物素A(1),irisolidone(2),染料木黄酮(3),sissotrin(4),槐糖苷( 5),genistin(6),tectoridin(7),apigenin(8),queccitrin(9)和rutin(10)。每种化合物的结构均通过多种光谱方法确定。在这些化合物中,1、3和7对花生四烯酸(AA)和U46619诱导的血小板凝集表现出约2.5-6.5倍的更大抑制作用(IC50:19.9和99.8 microM; 20.3和53.8 microM; 25.9和123.4 microM)比乙酰水杨酸(ASA,IC50:63.0和350.0 microM)。在AA和U46619诱导的聚集上,化合物2是比ASA强约22-40倍的抑制剂(IC50:分别为1.6和15.6 microM)。

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