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TitleThe structure of the major anthocyanin in Arabidopsis thaliana
Publication TypeJournal Article
Year of Publication2002
AuthorsBloor, S.J., and Abrahams S.
JournalPhytochemistry
Volume59
Issue3
Pagination343 - 346
Date Published2002
ISSN00319422 (ISSN)
Keywordsanthocyanin, Anthocyanins, Arabidopsis, Arabidopsis thaliana, article, Brassicaceae, carbon nuclear magnetic resonance, chemical structure, chemistry, Chromatography, High Pressure Liquid, coumarin derivative, Coumarins, cyanidin 3 O 2 O(2 O (sinapoyl) xylopyranosyl) 6 O (4 O (glucopyranosyl) p coumaroyl glucopyranoside) 5 O 6 O (malonyl) glucopyranoside, cyanidin 3 o [2 o [2 o (sinapoyl) beta dextro xylopyranosyl] 6 o [4 o (beta dextro glucopyranosyl) 4 coumaroyl beta dextro glucopyranoside] 5 o [6 o (malonyl) beta dextro glucopyranoside], cyanidin-3-O-2-O(2-O-(sinapoyl)-xylopyranosyl)-6-O-(4-O-(glucopyranosyl)-p-coumaroyl-glucopyranoside) 5-O-6-O-(malonyl)-glucopyranoside, electrospray mass spectrometry, Extraction, flavonol derivative, flower, glycoside, Glycosides, glycosylation, high performance liquid chromatography, Magnetic Resonance Spectroscopy, malonic acid, Mass spectrometry, Matthiola, matthiola incana, Molecular Structure, nonhuman, nuclear magnetic resonance spectroscopy, oligosaccharide, Oligosaccharides, para coumaric acid, plant, plant leaf, plant stem, proton nuclear magnetic resonance, sinapic acid, Spectrometry, Mass, Electrospray Ionization, structure analysis, unclassified drug
AbstractThe major anthocyanin in the leaves and stems of Arabidopsis thaliana has been isolated and shown to be cyanidin 3-O-[2-O(2-O-(sinapoyl)-β-D-xylopyranosyl)-6-O-(4-O-(β-D- glucopyranosyl)-p-coumaroyl-β-D-glucopyranoside] 5-O-[6-O-(malonyl) β-D-glucopyranoside]. This anthocyanin is a glucosylated version of one of the anthocyanins found in the flowers of the closely related Matthiola incana. © 2002 Elsevier Science Ltd. All rights reserved.
URLhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0037138279&partnerID=40&md5=d35cdc34bfc2d4be87554ea19daa1dc7
DOI10.1016/S0031-9422(01)00460-5

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