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Fig. 4 | BMC Complementary and Alternative Medicine

Fig. 4

From: Antioxidant and Cytoprotective effects of Pyrola decorata H. Andres and its five phenolic components

Fig. 4

Results 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 dimer

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