Chinese Journal of Magnetic Resonance

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NMR Assignments of Two Minor Ginsenosides Extratced from Panax notoginseng (Burk.) F. H. Chen

HUANG Gui-kun1,QIU Li1,2,3*,JIAO Yang1,YUAN Jing-quan1,2,3,XIE Ji-zhao1,MIAO Jian-hua2   

  1. 1. College of Pharmacology, Guangxi Medical University, Nanning 530021, China;
    2. Guangxi Institute of Medical Plant, Nanning 530023, China;
    3. Institute of Traditional Chinese Medicine and Natural Products, Jinan University, Guangzhou 510632, China
  • Received:2013-10-09 Revised:2014-07-19 Online:2014-09-05 Published:2014-09-05
  • Supported by:

    广西壮族自治区自然科学青年基金资助项目(2013GXNSFBB053001),广西药用植物园青年科学基金资助项目(桂药基201101).

Abstract:

Two ginsenosides were isolated from the 80% ethanol extract of the root of Panax notoginseng, namely 6-O-(β-D-glucopyranosyl)-20-O-(β-D-xylopyranosyl)-3β,6α,12β,20(S)-tetrahydroxydammar-24-ene (compound 1) and notoginsenoside U (compound 2). Their structures were elucidated by one-imensional and two-dimensional NMR (i.e., 1H-1H COSY, HSQC and HMBC) experiments. The 13C NMR spectral data of compound 1 was compared with those reported in the previous references, and corrections were made for some previous assignments which were incorrect. The completed assignments of
compound 1 were obtained. The 1H and 13C NMR signals of compound 2 in prydine-d5 were assigned.

Key words: NMR, ginsenosides, Panax notoginseng, assignment

CLC Number: