Fig. 4From: Antioxidant and Cytoprotective effects of Pyrola decorata H. Andres and its five phenolic componentsResults of UPLC-ESI-Q-TOF-MS/MS analysis. a Chromatogram of proto catechuic acid-protocatechuic acid dimer after the extraction of [C14H10O8-H]−.a1 Primary MS spectra of protocatechuic acid-protocatechuic acid dimer. a2 Secondary MS spectra of protocatechuic acid-protocatechuic acid dimer. b Chromatogram of gallic acid-gallic acid dimer after the extraction of [C14H10O10-H]−. (B1) Primary MS spectra of gallic acid-gallic acid dimer. c Chromatogram of hyperoside-hyperoside dimer after the extraction of [C42H38O24-H]−. c1 Primary MS spectra of hyperoside-hyperoside dimer. c2 Secondary MS spectra of hyperoside-hyperoside dimer. d Chromatogram of 2′′-O-galloylhyperin-2′′-O-galloylhyperin dimer after the extraction of [C56H46O32-H]−. d1 Primary MS spectra of 2′′-O-galloylhyperin-2′′-O-galloylhyperin dimer. d2 Secondary MS spectra of 2′′-O-galloylhyperin-2′′-O-galloylhyperin dimer. e Chromatogram of quercetin-quercetin dimer upon extraction of [C30H18O14-H]−. e1 Primary MS spectra of quercetin-quercetin dimer. e2 Secondary MS spectra of quercetin-quercetin dimerBack to article page