Karikura M, Miyase T, Tanizawa H, Takino Y, Taniyama T, Hayashi T
School of Pharmaceutical Sciences, University of Shizuoka, Japan.
Chem Pharm Bull (Tokyo). 1990 Oct;38(10):2859-61. doi: 10.1248/cpb.38.2859.
The decomposition of ginsenoside Rb2 (Rb2) in the rat large intestine after oral administration was investigated in detail. A part of Rb2 was decomposed and six decomposition products (I-VI) were observed on thin-layer chromatogram. Among them, five products (I-V) were isolated, and identification of these compounds was done by carbon-13 nuclear magnetic resonance (13C-NMR). On the basis of 13C-NMR analysis, these compounds were identified as ginsenoside Rd (I), 3-O-beta-D-glucopyranosyl-20-O- [alpha-L-arabinopyranosyl(1----6)-beta-D-glucopyranosyl]-20(S)- proto-panaxadiol (II), ginsenoside F2 (III), 20-O-[alpha-L-arabinopyranosyl(1----6)-beta-D-glucopyranosyl]-20(S )- protopanaxadiol (IV), and compound K (V), respectively.
详细研究了人参皂苷Rb2(Rb2)口服给药后在大鼠大肠中的分解情况。一部分Rb2发生分解,在薄层色谱图上观察到六种分解产物(I - VI)。其中,分离出了五种产物(I - V),并通过碳 - 13核磁共振(13C - NMR)对这些化合物进行了鉴定。基于13C - NMR分析,这些化合物分别被鉴定为人参皂苷Rd(I)、3 - O - β - D - 吡喃葡萄糖基 - 20 - O - [α - L - 阿拉伯吡喃糖基(1→6)- β - D - 吡喃葡萄糖基] - 20(S)- 原人参二醇(II)、人参皂苷F2(III)、20 - O - [α - L - 阿拉伯吡喃糖基(1→6)- β - D - 吡喃葡萄糖基] - 20(S)- 原人参二醇(IV)和化合物K(V)。