Raman spectroscopy study on the structure of ginsenoside Rg3

被引:0
|
作者
Qu Xiao-bo [1 ,2 ]
Zhao Yu [2 ]
Song Yan [2 ,3 ]
Zhang Wei [3 ]
Zhao Bing [3 ]
Li Yu-xin [1 ]
机构
[1] NE Normal Univ, Inst Cytol & Genet, Changchun 130024, Peoples R China
[2] Changchun Univ Tradit Chinese Med, Ctr New Drugs Res, Changchun 130117, Peoples R China
[3] Jilin Univ, State Key Lab Supramol Struct & Mat, Minist Educ, Changchun 130012, Peoples R China
关键词
ginsenoside Rg3; Raman spectrum; isomer;
D O I
暂无
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Ginsenoside Rg3, discovered from Red Panax ginseng, is a new anticancer agent, which shows inhibitive activities of tumor metastasis in mice and in vitro tumor cell invasion. There are two isomers for ginsenoside Rg3: 20-(R)-Rg3 and 20-(S)Rg3. The research on the Rg3 structure is limitted, with no report on the use of Raman spectroscopy in such molecules. In the present article, the authors employed the Raman spectroscopy to study the structure of ginsenoside Rg3. Compared with 20-(R)Rg3, the hydrocarbon chain of 20-(S)-Rg3 is located in the inner of molecules. In addition, there are significant differences in band location and relative intensity between the spectra of 20-(R)-Rg3 and 20-(S)-Rg3, and this indicates that Raman spectroscopy can be used as a simple, fast and accurate analytical tool to identify ginsenoside Rg3 isomers.
引用
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页码:569 / 571
页数:3
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