Skip to main content
. 2020 Jul 2;9(7):573. doi: 10.3390/antiox9070573

Table 2.

Compounds identified in polyphenol-rich extracts from medicinal plants.

Medicinal Plant Retention Time (min) Molecular Weight (Da) Parent Ions Fragment Ions Identified Compound
A. borbonica 2.5 354 353 191 Chlorogenic acid isomer
3.5 354 353 191 Chlorogenic acid
3.7 354 353 191, 173 Chlorogenic acid isomer
5.7 610 609 301 Quercetin-hexoside-ramnoside
6.0 594 593 447, 285 Kaempferol-hexoside-ramnoside
6.2 594 593 455, 285 Kaempferol-hexoside-ramnoside
6.4 516 515 353, 191 Dicaffeoylquinic acid
6.6 516 515 353, 191 Dicaffeoylquinic acid
6.9 516 515 353, 191 Dicaffeoylquinic acid
A. triplinervis 3.2 154 153 109 Protocatechuic acid
4.4 180 179 / Caffeic acid
5.0 356
610
355
609
193
301, 179
Feruoyl-hexoside
Quercetin-hexoside-ramnoside
5.2 464 463 301 Quercetin-hexoside
5.5 550 549 505, 463, 301 Quercetin-hexoside-malonate
6.1 696 695 533, 515, 371, 209 Tricaffeoyl-glucarate
6.3 194 193 / Isoferulic acid
6.8 190 191 * 163, 133 * Ayapin
7.4 176 177 * 145, 133, 121 * Ayapanin (Herniarin)
T. bentzoe 1.2 482 481 301 Hexahydroxydiphenoyl (HHDP)-hexoside
1.4 482 481 301 HHDP-hexoside
2.3 170 169 125 Gallic acid
2.7 782 781 721, 601, 299, 271 Punicalin
3.0 934 933 / Galloyl-punicalin
3.2 934 933 915, 781, 721, 601 Galloyl-punicalin
3.4 470 469 425 Valoneic acid dilactone
3.5 1084 1083 781, 601 Punicalagin
3.8 1084 1083 781, 601 Punicalagin
3.9 186 1085 783, 601, 451 Digalloyl-gallagyl-hexoside
4.0 634 633 463, 301 HHDP-galloyl-hexoside
4.1 1086 1085 933, 721, 601 Digalloyl-punicalin
4.3 786 785 633, 483 HHDP-digalloyl-hexoside
4.9 938 937 785, 767, 741, 465, 301 Tri-galloyl-HHDP-glucose
5.2 302 301 / Ellagic acid
5.3 940 939 787, 769, 617 Pentagalloyl-hexoside
D. viscosa 3.8 1152 1151 981, 863, 711 Procyanidin tetramer type A
4.2 578 557 451, 425 Procyanidin dimer B2
4.6 864 863 711, 693, 559 Procyanidin trimer type A
5.4 624 623 315 Isorhamnetin-hexoside-rhamnoside
9.0 344 343 329, 301, 283 5,7-Dihydroxy-3,6,4′-trimethoxyflavone (Santin)

Polyphenol-rich extracts from medicinal plants were analyzed by UPLC-ESI-MS-MS at 280 nm. The phytochemicals were detected according to their retention time and the m/z ratio of their parent ions [M − H] and fragments at negative mode, except for the parent ions [M + H]+ and fragments that were detected at positive mode and indicated by *.