NMR spectral assignments of a new [C--O--C] isoflavone dimer from Andira surinamensis
Copyright (c) 2007 John Wiley & Sons, Ltd.
Publié dans: | Magnetic resonance in chemistry : MRC. - 1985. - 46(2008), 1 vom: 01. Jan., Seite 103-6 |
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Auteur principal: | |
Autres auteurs: | , |
Format: | Article en ligne |
Langue: | English |
Publié: |
2008
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Accès à la collection: | Magnetic resonance in chemistry : MRC |
Sujets: | Journal Article Isoflavones Powders |
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 |
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Description: | Date Completed 25.04.2008 Date Revised 20.07.2009 published: Print Citation Status MEDLINE |
ISSN: | 1097-458X |