Phenolic Metabolites of Karwinskia humboldtiana Leaves

Page: 1143

P. Mučajia, M. Nagya, F. Šeršeňb, E. Švajdlenkac, J. Drozdc, M. Štujberd, and T. Liptajd

a Department of Pharmacognosy and Botany, Faculty of Pharmacy, Comenius University, Bratislava, b Institute of Chemistry, Faculty of Natural Sciences, Comenius University Bratislava, c Institute of Natural Drugs, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences, Brno, d Department of NMR and MS Spectroscopy, Faculty of Chemical and Food Technology, Slovak Technical University, Bratislava


Methanolic extract from leaves of Karwinskia humboldtiana (Schult.) Zucc. was subjected to fractionation with a pair of immiscible solvents and subsequently tested for antioxidant activity. Using DPPH the order of scaven¬ging activities of the extracts in comparison with standards of L-ascorbic acid and quercetin was as follows: ethyl acetate fraction > L-ascorbic acid > quercetin > butan-1-ol > light petrol > chloroform > water. The capability of scavenging OH radicals determined by EPR was as follows: ethyl acetate, chloroform > light petrol > butan-1-ol > water fractions. On the basis of availability and antioxidant activity of these fractions, isolation of constituents from butanol fractions was achieved. Separation of this fraction led to the isolation of (+)-epicatechin and flavonol derivatives – quercetin, quercetin 3-O-glucoside (isoquercitrin), quercetin-3-O-galac¬toside (hyperosid), quercetin-3-O-ara¬binoside, quercetin 3-O-rutinoside (rutin), kaempferol 3-O-arabinoside and kaempferol 3-O-rutinoside. All of them might be responsible for the observed antioxidant effects.


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