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

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 chroma...

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Detalles Bibliográficos
Autores principales: Wang, Yu-Shuai, Jin, Yin-Ping, Gao, Wei, Xiao, Sheng-Yuan, Zhang, Yu-Wei, Zheng, Pei-He, Wang, Jia, Liu, Jun-Xia, Sun, Cheng-He, Wang, Ying-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005357/
https://www.ncbi.nlm.nih.gov/pubmed/27616900
http://dx.doi.org/10.1016/j.jgr.2015.08.003
Descripción
Sumario: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 (1)H- and (13)C-NMR spectra were found to be inaccurate. CONCLUSION: This study reports the complete NMR assignment of malonyl-ginsenoside Re, Rb(1), Rb(2), Rc, and Rd for the first time.