“…Gallic acid (peak 1), myricetin-3-O-glucoside (peak 3), quercetin-3-O-rutinoside (peak 4), quercetin-3-O-glucoside (peak 7), ellagic acid (peak 8), kaempherol-3-O-rutinoside (peak 9), isorhamnetin-3-O-rutinoside (peak 10), and quercetin-3-O-rhamnoside (peak 11), were positively identified in comparison with the DAD and MS spectrums of the commercial phenolic compounds standards (Extrasynthese, Genay, France). [43,44], burs [6,8,25,45], leaves [46], and heartwood [47,48]. The only ellagitannin found corresponded to peak 2 ([M-H] − at m/z 937) and was identified as a trigalloyl-HHDP-glucose, also known as chestanin A, with a characteristic MS 2 fragment at m/z 301 (ellagic acid) and suffered the loss of gallic acid (m/z 767) and the fragments m/z 635 and 465 were ascribed to the loss of hexahydroxydiphenoyl (HHDP) and gallic acid.…”