Quantitative studies on structure–ORAC relationships of anthocyanins from eggplant and radish using 3D-QSAR

Abstract

The 3-dimensional quantitative structure activity relationship (3D-QSAR) models were established from 21 anthocyanins based on their oxygen radical absorbing capacity (ORAC) and were applied to predict anthocyanins in eggplant and radish for their ORAC values. The cross-validated q2=0.857/0.729, non-cross-validated r2=0.958/0.856, standard error of estimate=0.153/0.134, and F=73.267/19.247 were for the best QSAR (CoMFA/CoMSIA) models, where the correlation coefficient r2pred=0.998/0.997 (>0.6) indicated a high predictive ability for each. Additionally, the contour map results suggested that structural characteristics of anthocyanins favourable for the high ORAC. Four anthocyanins from eggplant and radish have been screened based on the QSAR models. Pelargonidin-3-[(6′′-p-coumaroyl)-glucosyl(2→1)glucoside]-5-(6′′-malonyl)-glucoside, delphinidin-3-rutinoside-5-glucoside, and delphinidin-3-[(4′′-p-coumaroyl)-rhamnosyl(1→6)glucoside]-5-glucoside potential with high ORAC based the QSAR models were isolated and also confirmed for their relative high antioxidant ability, which might attribute to the bulky and/or electron-donating substituent at the 3-position in the C ring or/and hydrogen bond donor group/electron donating group on the R1 position in the B ring.