Related Experiment Video
Updated: Aug 9, 2026

Biosynthesis of a Flavonol from a Flavanone by Establishing a One-pot Bienzymatic Cascade
Published on: August 14, 2019
High-performance liquid chromatographic identification of flavonoid monoglycosides from Prunus serotina ehrh
1Department of Pharmacognosy, Faculty of Pharmacy, Medical University of Lódź, 1 Muszyńiski St., 90-151 Lódź, Poland. molszewska@pharm.am.lodz.pl
Abstract:
Five minor flavonoid monosides, glycosides of quercetin and kaempferol, together with three previously isolated compounds were identified cochromatographically in P. serotina Ehrh. leaves and flowers (inflorescences) using RP-HPLC and TLC techniques and finally determined as quercetin 3-O-alpha-L-arabinofuranoside (avicularin), 3-O-alpha-L-arabinopyranoside (guaijaverin), 3-O-beta-D-xylopyranoside (reynoutrin), 3-O-beta-D-glucopyranoside (isoquercitrin), 3-O-beta-D-galactopyranoside (hyperoside) followed by kaempferol 3-O-alpha-L-arabinofuranoside (juglanin), 3-O-beta-D-xylopyranoside and 3-O-beta-D-glucopyranoside (astragalin). Moreover, two further minor flavonols were isolated from the leaves, characterized by hydrolysis experiments, UV and 1H NMR spectroscopy, and identified finally as isorhamnetin 3-O-alpha-arabinofuranoside and isorhamnetin 3-O-beta-xylopyranoside, the rare natural products.