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黄花倒水莲皂甙Reinioside C在大鼠体内代谢产物的鉴定
引用本文:张东明,宫濑敏男,野口博司,谷泽久之,马万云,陈瓞延.黄花倒水莲皂甙Reinioside C在大鼠体内代谢产物的鉴定[J].高等学校化学学报,2002,23(1):63-67.
作者姓名:张东明  宫濑敏男  野口博司  谷泽久之  马万云  陈瓞延
作者单位:1. 清华大学物理系单原子分子测控教育部重点实验室, 北京 100084; 2. 静冈县立大学药学院, 静冈 422, 日本
基金项目:国家自然科学基金 (批准号 :30 0 70 2 0 9)资助
摘    要:为了探讨五环三萜皂甙ReiniosideC在大鼠体内代谢产物的结构,单剂量口服ReiniosideC,5h后放血处死,用制备型高效液相色谱方法对血液和各脏器进行提取分离,从大肠内容物和粪中,分离得到了7种代谢产物.用FAB-MS,1H NMR和13C NMR方法鉴定了它们的结构.

关 键 词:Reinioside  C  皂甙  黄花倒水莲  代谢物  
文章编号:0251-0790(2002)01-0063-05
收稿时间:2000-09-11

Identification of Metabolites of Reinioside C, A Triterpene Saponin from the Roots of Polygala fallax Hemsl
ZHANG Dong Ming ,Miyase Toshio Noguchi Hiroshi ,Tanizawa Hisayuki ,MA Wan Yun ,CHEN Die Yan.Identification of Metabolites of Reinioside C, A Triterpene Saponin from the Roots of Polygala fallax Hemsl[J].Chemical Research In Chinese Universities,2002,23(1):63-67.
Authors:ZHANG Dong Ming  Miyase Toshio Noguchi Hiroshi  Tanizawa Hisayuki  MA Wan Yun  CHEN Die Yan
Institution:1. Key Laboratory of or Single Atomicand Molecular Detectionof Educational Ministry, Department of Physics, Tsinghua University, Beijing 100084, China; 2. School of Pharmaceutical Sciences, Universityof Shizuoka, 5221, Yada Shizuoka 422, Japan
Abstract:Triterpene saponins were widely distributed in the oriental traditional crude drugs, which play important roles as anti-inflammatory, anticancer and antihepatitis agent. For example, from Ginseng Radix, Bupleuri Radix, Polygalae Radix, Platycodi Radix etc, many bioactive and available triterpene saponins were obtained and they could explain the effect of the crude drug. However metabolic transformation of triterpene saponin in vivo have not been reported. We studied the metabolism of reinioside C, a triterpene saponin from the roots of Polygala fallax Hemsl in rats. After oral administration of reinioside C, seven metabolites(RA-RG) of reinioside Cwere obtained from the content of large intestin and feces. The structures of metabolites were elucidated as 28-O-α Lrhamnopyranosyl-(1→2)-(3,4 diacetyl)-β-Dfucopyranosyl presenegin, 28-O-β-Dxylopyranosyl-(1→4)-α-Lrhamnopyranosyl-(1→2)-(3,4 diacetyl)-β-Dfucopyranosyl presenegin, 28-O-α-Lrhamnopyranosyl-(1→2) (3,4-diacetyl)-β-Dfucopyranosyl presenegin3 O-β-Dglucopyranosyl-(1→2)-β-Dglucopy ranoside, 28-O-β-Dxylopyranosyl-(1→4)-α-Lrhamnopyranosyl-(1→2)-β-D-fucopyranosyl presenegin 3-O-β-Dglucopyranosyl-(1→2)-β-Dglucopyranoside, 28-O-β-Dxylopyranosyl-(1→4)-α-Lrhamnopy ranosyl-(1→2)-(3 acetyl)-β-D-fucopyranosyl presenegin-3-O-β-D-glu copyranosyl-(1→2)-β-D-glucopyranoside, 28-O-β-D-xylopyranosyl-(1→4)-α-Lrhamnopyranosyl-(1→2)-(4 acetyl)-β-D-fucopyranosyl pre senegin3 O-β-D-glucopyranosyl-(1→2)-β-Dglucopyranoside, 28-O-β-D-fucopyranosyl presenegin, respectively, on the basis of spectroscopic data.
Keywords:Reinioside C  Triterpene saponin  Polygala fallax  Metabolite  
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