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Isolation Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity

机译:人参皂苷衍生物的分离合成结构及其抗肿瘤活性

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摘要

Protopanaxatriol saponins obtained with AB-8 macroporous resin mainly consisted of ginsenosides Rg1 and Re. A novel mono-ester of ginsenoside-Rh1 (ginsenoside-ORh1) was synthesized through further enzymatic hydrolysis and octanoyl chloride modifications. A 53% yield was obtained by a facile synthetic method. The structures were identified on the basis of 1D-NMR and 2D-NMR, as well as ESI-TOF-MS mass spectroscopic analyses. The isolated and synthetic compounds were applied in an anti-tumor bioassay, in which ginsenoside ORh1 showed moderate effects on Murine H22 Hepatoma Cells.
机译:用AB-8大孔树脂制得的普萘托那三醇皂苷主要由人参皂苷Rg1和Re组成。通过进一步的酶促水解和辛酰氯的修饰,合成了一种新的人参皂苷-Rh1单酯(人参皂苷-ORh1)。通过简便的合成方法获得53%的收率。根据1D-NMR和2D-NMR以及ESI-TOF-MS质谱分析鉴定结构。分离和合成的化合物用于抗肿瘤生物测定中,其中人参皂甙ORh1对小鼠H22肝癌细胞具有中等程度的作用。

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