Neacsu Madalina, Micol Vicente, Pérez-Fons Laura, Willför Stefan, Holmbom Bjarne, Mallavia Ricardo
Department of Chemistry and Biochemistry, University of Agricultural Sciences and Veterinary Medicine, Manastur 3-5, 400372 Cluj, Napoca, Romania.
Molecules. 2007 Feb 19;12(2):205-17. doi: 10.3390/12020205.
The complete characterization of two compounds obtained from the acetone extract of Populus tremula knotwood has been was achieved using LC-DAD-MS, MS/MS, IR and NMR. The new compounds were unequivocally identified as a mixture of the ester isomers of the (E) and (Z) p-coumarate of 1-O-rutinose. The isomers showed the capacity to inhibit lipid peroxidation induced by tert-butylhydroperoxide and to trap peroxyl radicals, as determined by a chemiluminescence method. These new phenyl disaccharides also showed a significant ORAC (oxygen radical absorbance capacity) value, i.e. 11.7 microM TE (Trolox Equivalents).