“…Four compounds 20 (t r =45 min), 22 (t r = 46.1 min), 24 (t r = 47.8 min), and 26 (t r = 50.3 min) with UV and MS spectra ([M-H] − ion with m/z 515 and fragment ions with m/z 353 and 191) were assigned the structure di-O-caffeoylquinic acids (1,4-di-O-CQA, 3,4-di-O-CQA, 3,5-di-O-CQA, 1,5-di-O-CQA or 4,5-di-O-CQA) (Eisenman et al, 2011;Miron et al, 2011;Gu et al, 2012;Lin and Harnly, 2012;Olennikov et al, 2018;Olennikov et al, 2019). Further, compounds 2 (t r = 12 min), 3 (t r = 12.2 min), 4 (t r = 13.4 min), 10 (t r = 25 min) and 13 (t r = 34.9 min) gave pseudomolecular ions m/z [M−H] -477, 371, 359, 355, respectively, and were tentatively identified as protocatechuic acid dihexoside, caffeoyl hexaric acid, syringic acid hexoside, and ferulic acid hexoside, respectively (Barros et al, 2012;Mekky et al, 2019;Kiss et al, 2020). Flavonoid glycosides were assigned as derivatives of isorhamnetin (Miron et al, 2011;Lin and Harnly, 2012), apigenin (Lin and Harnly, 2012), patuletin (Vienne et al, 1989;Lin and Harnly, 2012), and quercetin (Obolskiy et al, 2011;Lin and Harnly, 2012).…”