Journal of Ginseng Research (Jul 2016)

Complete 1H-NMR and 13C-NMR spectral assignment of five malonyl ginsenosides from the fresh flower buds of Panax ginseng

  • Yu-Shuai Wang,
  • Yin-Ping Jin,
  • Wei Gao,
  • Sheng-Yuan Xiao,
  • Yu-Wei Zhang,
  • Pei-He Zheng,
  • Jia Wang,
  • Jun-Xia Liu,
  • Cheng-He Sun,
  • Ying-Ping Wang

DOI
https://doi.org/10.1016/j.jgr.2015.08.003
Journal volume & issue
Vol. 40, no. 3
pp. 245 – 250

Abstract

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Background: Ginsenosides are the major effective ingredients responsible for the pharmacological effects of ginseng. Malonyl ginsenosides are natural ginsenosides that contain a malonyl group attached to a glucose unit of the corresponding neutral ginsenosides. Methods: Medium-pressure liquid chromatography and semipreparative high-performance liquid chromatography were used to isolate purified compounds and their structures determined by extensive one-dimensional- and two-dimensional nuclear magnetic resonance (NMR) experiments. Results: A new saponin, namely malonyl-ginsenoside Re, was isolated from the fresh flower buds of Panax ginseng, along with malonyl-ginsenosides Rb1, Rb2, Rc, Rd. Some assignments for previously published 1H- and 13C-NMR spectra were found to be inaccurate. Conclusion: This study reports the complete NMR assignment of malonyl-ginsenoside Re, Rb1, Rb2, Rc, and Rd for the first time.

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