Acylated cyanidin 3-sambubioside-5-glucosides in Matthiola incana
1995
Saito, N. | Tatsuzawa, F. | Nishiyama, A. | Yokoi, M. | Shigihara, A. | Honda, T.
Four acylated cyanidin 3-sambubioside-5-glucosides were isolated from purple-violet flowers of Matthiola incana and their structures were determined by chemical and spectroscopic methods. Three acylated anthocyanins were cyanidin 3-O-(6-O-acyl-24-(2-O-sinapyl-beta-D-xylopyranosyl) beta-D-glucopyranoside)5-O-(6-O-malonyl-beta-D-glucopyranosides), in which the acyl group is p-coumaryl, caffeyl or ferulyl, respectively. The remaining pigment is free from malonic acid and was identified as cyanidin 3-0-(6-0-trans-ferulyl-2-O-(2-O-trans-sinapyl-beta-D-xylopyranosyl) beta-D-glucopyranoside)5-O-(beta-D-glucopyranoside). Analysis of the anthocyanin constituents in 16 purple-violet cultivars revealed that they contained the above triacylated anthocyanins in variable amounts as main pigments. An aromatic pair of pigments containing sinapic and ferulic acids are considered to produce an important intramolecular effect, making bluish colours in these flowers.
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