| Literature DB >> 17988698 |
Regina Anero1, Ana Díaz-Lanza, Evelyne Ollivier, Béatrice Baghdikian, Guy Balansard, Manuel Bernabé.
Abstract
Six monoterpene glycosides were isolated from Fadogia agrestis. Their structures were elucidated using a combination of mass spectroscopy, 1D- and 2D-homo- and hetero-NMR spectroscopy and chemical analysis, and established as being derivatives of 2,6-dimethyl-2(E),6(Z)-octadiene-1,8-diol containing from two to four units of rhamnopyranose and, three of them, one or two additional units of glucopyranose. In three of the compounds an acyl group of 8-hydroxy-2,6-dimethyl-2(E),6(Z)-octadienoyl was found esterifying the O-2 position of one of the units of rhamnopyranose.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17988698 DOI: 10.1016/j.phytochem.2007.09.024
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072