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Lipidated Steroid Saponins from Dioscorea villosa (Wild Yam)

机译:薯Di类脂类固醇皂苷(野生山药)

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摘要

Two groups of lipidated steroid saponins including seven new compounds (>2, >3, >5, and >7–10) were isolated from the widely used botanical, wild yam (Dioscorea villosa), employing a fractionation protocol of metabolomic mining. This methodology has very recently led to the isolation of 14 diarylheptanoids from the same plant. Together with these lipidated steroid saponins, they establish additional new markers for Dioscorea villosa. The lipidation of steroids with analogue long-chain fatty acids containing different degrees of unsaturation generates entire series of compounds which are difficult to purify and analyze. The structures of the two series of lipidated steroid saponins (series A and B) were demonstrated by a combination of 1D and 2D NMR as well as GC-MS after chemical modification. Series A was determined to be a mixture of lipidated spirostanol glycosides (>1–5), while series B (>6–10) proved to be a mixture of five lipidated clionasterol glucosides. The latter group represents the first derivatives of clionasterol to be found in D. villosa. The discovery of this specific structural type of aliphatic esters of steroid saponins expands the characterization of the secondary metabolome of D. villosa. It also may inspire biological studies which take into account the lipophilic character and significantly altered physiochemical characteristics of these otherwise relatively polar phytoconstituents.
机译:两组脂化类固醇皂苷,包括七个新化合物(> 2 ,> 3 ,> 5 和> 7-10 )采用代谢组学分馏方案从广泛使用的植物野生山药(Dioscorea villosa)中分离得到。最近,这种方法导致从同一植物中分离出14种二芳基庚烷类化合物。它们与这些脂化的类固醇皂苷一起,为薯Di提供了新的标记。用含有不同程度不饱和度的类似长链脂肪酸对类固醇进行脂化,会产生一系列难以纯化和分析的化合物。化学修饰后,通过1D和2D NMR以及GC-MS的组合证明了两个系列的脂化类固醇皂苷(系列A和B)的结构。已确定A系列是脂化的螺固醇糖苷(> 1-5 )的混合物,而B系列(> 6–10 )被证明是五种脂化的香豆甾醇糖苷的混合物。后一组代表在D. villosa中发现的可可固醇的第一衍生物。类固醇皂苷脂族酯的这种特定结构类型的发现扩展了绒毛线虫的次级代谢组的表征。它也可能激发生物学研究,这些研究考虑了这些原本相对极性的植物成分的亲脂性和显着改变的理化特性。

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