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来自蔓生白前的孕甾烷糖苷。

Pregnane glycosides from Cynanchum menarandrense.

作者信息

Tsoukalas Michail, Psichas Arianna, Reimann Frank, Gribble Fiona M, Lobstein Annelise, Urbain Aurélie

机构信息

Pharmacognosy and Bioactive Natural Products, Université de Strasbourg, CNRS, LIT UMR 7200, F-67000 Strasbourg, France.

Metabolic Research Laboratories and MRC Metabolic Diseases Unit, WT-MRC Institute of Metabolic Science, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, UK.

出版信息

Steroids. 2017 Sep;125:27-32. doi: 10.1016/j.steroids.2017.06.005. Epub 2017 Jun 19.

Abstract

Five new pregnane-type steroidal glycosides, named menarandrosides A-E (1-2, 5-7) were isolated from the aerial parts of Cynanchum menarandrense, together with three known compounds, carumbelloside I (3), carumbelloside II (4), and pregnenolone-3-O-gentiobioside (8). Their structures were determined on the basis of spectroscopic analyses including NMR and mass spectrometry, reporting C-21 steroids glycosylated only by one or two glucose moieties. Compounds were then investigated for their potential to stimulate glucagon-like peptide-1 (GLP-1) secretion in intestinal cells; although none of the pure compounds had any influence, the fraction enriched in pregnanes exhibited a significant activity, suggesting a possible synergistic effect. Furthermore, none of the purified compounds affected cell viability.

摘要

从蔓生白前地上部分分离得到5个新的孕甾烷型甾体糖苷,命名为蔓生白前苷A-E(1-2、5-7),同时还得到3个已知化合物,即胡萝卜苷I(3)、胡萝卜苷II(4)和孕烯醇酮-3-O-龙胆二糖苷(8)。通过包括核磁共振(NMR)和质谱分析在内的光谱分析确定了它们的结构,报道了仅由一个或两个葡萄糖部分糖基化的C-21甾体。然后研究了这些化合物在肠细胞中刺激胰高血糖素样肽-1(GLP-1)分泌的潜力;尽管没有一种纯化合物有任何影响,但富含孕甾烷的部分表现出显著活性,表明可能存在协同效应。此外,没有一种纯化的化合物影响细胞活力。

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