首页> 美国卫生研究院文献>Molecules >Structures and Biogenesis of Fallaxosides D4 D5 D6 and D7 Trisulfated Non-Holostane Triterpene Glycosides from the Sea Cucumber Cucumaria fallax
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Structures and Biogenesis of Fallaxosides D4 D5 D6 and D7 Trisulfated Non-Holostane Triterpene Glycosides from the Sea Cucumber Cucumaria fallax

机译:海参黄瓜fallax的fallaxosides D4D5D6和D7三硫酸化的非硫酸胆甾烷三萜糖苷的结构和生物发生

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摘要

Four new trisulfated triterpene glycosides, fallaxosides D4 (>1), D5 (>2), D6 (>3) and D7 (>4) have been isolated from the sea cucumber Cucumaria fallax (Cucumariidae, Dendrochirotida). The structures of the glycosides have been elucidated by 2D NMR spectroscopy and HRESIMS. All the glycosides have the lanostane aglycones of a rare non-holostane type with 7(8)-, 8(9)- or 9(11)-double bonds, one or two hydroxyl groups occupying unusual positions in the polycyclic nucleus and shortened or normal side chains. The pentasaccharide carbohydrate moieties of >1–>4 have three sulfate groups. The cytotoxic activity of glycosides >1–>4 against the ascite form of mouse Ehrlich carcinoma cells and mouse spleen lymphocytes and hemolytic activity against mouse erythrocytes have been studied.
机译:四个新的三硫酸化三萜糖苷,法拉第糖苷D4(> 1 ),D5(> 2 ),D6(> 3 )和D7(> 4 < / strong>)已从海参黄瓜(Cucumaria fallax)(Cucumariidae,Dendrochirotida)中分离出来。糖苷的结构已通过2D NMR光谱和HRESIMS进行了阐明。所有的糖苷均具有罕见的非全甾烷类型的羊毛甾烷苷元,具有7(8)-,8(9)-或9(11)-双键,一个或两个羟基在多环核中占据不寻常的位置,并缩短或缩短正常的侧链。 > 1 – > 4 的五糖碳水化合物部分具有三个硫酸盐基团。研究了糖苷> 1 – > 4 对小鼠艾氏癌细胞和小鼠脾淋巴细胞的腹水形式的细胞毒活性以及对小鼠红细胞的溶血活性。

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