Chinese Journal of Magnetic Resonance ›› 2006, Vol. 23 ›› Issue (4): 429-442.

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Application of NMR for Structural Dedication of Forbesoside

YANG Xiu-wei   

  1. (State Key Laboratory of Natural & Biomimetic Drugs, School of Pharmaceutical Sciences,Peking University, Beijing 100083, China)
  • Received:2006-03-06 Revised:2006-05-29 Published:2006-12-05 Online:2009-12-05
  • Contact: Yang Xiu-wei

Abstract: A series of 1D (1H and 13C NMR, DEPT experiment) and 2D NMR (including gCOSY, gHSQC and gHMBC) techniques were applied to the assignment of all proton and carbon signals of forbesoside [6′-O-(trans-feruloyl)-nodakenin] which was a new coumarins compound isolated from the underground parts of Notopterygium forbesii Boiss. and Notopterygium incisum Ting ex H. T. Chang and with anti-inflammatory bioactivity. The NMR signals changed rules from umbelliferone to 7-demethylsuberosin, nodakenetin, nodakenin and forbesoside, and of acyled hydroxymethyl moiety of glucopyranosyl group, and methods of NMR signals assignment of saccharide were discussed and summarized.

Key words: NMR, forbesoside, 6′-O-(trans-feruloyl)-nodakenin, umbelliferone, nodakenetin, Notopterygium forbesii and Notopterygium incisum

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