NMR spectral assignments of a new [C--O--C] isoflavone dimer from Andira surinamensis

Copyright (c) 2007 John Wiley & Sons, Ltd.

Détails bibliographiques
Publié dans:Magnetic resonance in chemistry : MRC. - 1985. - 46(2008), 1 vom: 01. Jan., Seite 103-6
Auteur principal: de Almeida, José Gustavo L (Auteur)
Autres auteurs: Silveira, Edilberto R, Pessoa, Otília Deusdênia L
Format: Article en ligne
Langue:English
Publié: 2008
Accès à la collection:Magnetic resonance in chemistry : MRC
Sujets:Journal Article Isoflavones Powders
Description
Résumé:Copyright (c) 2007 John Wiley & Sons, Ltd.
The phytochemical investigation of extracts from the branch wood and branch barks of Andira surinamensis yielded a novel isoflavone dimer, 4'-methoxyisoflavone-(7-O-7'')-3''',4'''-methylenedioxyisoflavone (surinamensin), along with the triterpene lupeol and the known isoflavones 5,7-dihydroxy-4'-methoxyisoflavone (biochanin A), 5,4'-dihydroxy-7-methoxyisoflavone (prunetin), 7,3'-dihydroxy-4'-methoxyisoflavone (calycosin), and 5,7,3'-trihydroxy-4'-methoxyisoflavone (pratensein). The structure of the new isoflavone was elucidated by 1D and 2D homonuclear and heteronuclear NMR spectroscopy and by comparison with published data for closely related compounds
Description:Date Completed 25.04.2008
Date Revised 20.07.2009
published: Print
Citation Status MEDLINE
ISSN:1097-458X