Chinese Journal of Magnetic Resonance ›› 1999, Vol. 16 ›› Issue (1): 44-51.

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NMR STUDY ON A NEW BIDESMOSIDIC TRITERPENOID GLYCOSIDE FROM DIPSOCUS ASPEROIDES

Miao Zhenchun1, Feng Rui1, Zhou Y ongxin1, Wei Feng2   

  1. 1 Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing 100850;
    2 Beijing Jiangzhong Pharmaceutical Institute, Beijing 100050
  • Received:1998-11-06 Revised:1998-12-14 Published:1999-02-05 Online:2018-01-11

Abstract: A new 3,28-bidesmosidic triterpenoid saponin was isolated from the ethanolic extract of the root of Dipsocus asperoides C.Y.Cheng et T.M.A. and its structure established as 3-O-[α-L-rhammopyranosyl(1→3)][-β-D-glycopranosyl(1→4)]-β-D-glycopranosy(1→3)-α-L-rhammopyranosyl (1→2)-β-L-arabinopyranosyl-hederagenin-28-O-β-D-glycopranosyl (1→6)-β-D-glycopranoside. The sites of glycosylation and the sequence of sugars in the glycoside can be determined unambiguously and total assignment of severely overlapping proton resonance of sugar residues were achieved by a combined use of the 1D SEMDY, NOE difference spectroscopy in rotating frame and selective long-range DEPT techniques.

Key words: 1H NMR sepectrum of sugar residue, Dipsocus asperoides, 3,28-bidesmosidic triterpenoid saponin, Structural determination of Oligosaccharide Chains, ROE difference spectroscopy, Selective long-range DEPT, 1D-SEMDY