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. 2021 Sep 16;10(9):1475. doi: 10.3390/antiox10091475

Table 5.

Tentative identification of phenolic compounds in AP extracts.

Proposed Compounds Class/Subclass Molecular Formula m/z Meas. RT (min) mSigma
Quinic acid Organic acid C7H12O6 191.0560 4.54 10.6
Tyrosol-hexoside-pentoside Phenylethanoids C19H28O11 431.1557 4.8 17.7
4-Hydroxybenzoic acid PA/HB C7H6O3 137.0241 5.04 10
Chlorogenic acid/caffeoyl-quinic acid PA/HC C16H18O9 353.0879 6.62 20.6
Benzoic acid PA/HB C7H6O2 121.0293 6.79 1.7
Procyanidin trimer B FL/flavanol oligomer C45H38O18 865.1973 6.86 48.2
Procyanidin dimer B FL/flavanol oligomer C30H26O12 577.1338 7.01 4.7
Catechin FL/flavanol C15H14O6 289.0717 7.99 4.1
Quercetin—dihexose FL/flavanol C27H30O17 625.1405 9.44 21.7
Quercetin O-arabinosyl-glucoside FL/flavanol C26H28O16 595.1300 10.46 7.9
Rutin FL/flavanol C27H30O16 609.1457 10.76 9.8
Nudiposide Lignan C27H36O12 551.2130 11.34 5.6
Epigallocatechin 3-coumarate FL/flavanol C24H20O9 451.1031 11.61 8.6
Taxifolin FL/flavanonol C15H12O7 303.0507 11.64 3.9
Quercetin FL/flavanol C15H10O7 301.0352 11.82 25.6
Quercetin 3-glucoside FL/flavanol C21H20O12 463.0881 11.85 4.3
Quercetin 3-glucuronide FL/flavanol C21H18O13 477.0674 11.94 12.7
Procyanidin dimer A FL/flavanol oligomer C30H24O12 575.1189 12.45 12
Kaempferol-hexose FL/flavanol C21H20O11 447.0931 13.14 22.9
Luteolin 7-O-(2″-O-pentosyl) hexoside FL/flavone C26H28O15 579.1354 13.49 9.1
Procyanidin trimer A FL/flavanol oligomer C45H36O18 863.1812 14.03 58.5
Kaempferol O-glucosyl-rhamnoside FL/flavanol C27H30O15 593.1505 14.49 12.5
Neosakuranetin FL/chalcone C22H24O10 44731298 14.62 11.9
p-coumaric acid PA/HC C9H8O3 163.0399 16.32 6.5
(±)-Naringenin FL/flavanone C15H12O5 271.0611 16.69 14.1

* Abbreviations: PA: phenolic acid; HB: hydroxybenzoic acid; HC: hydroxycinnamic acid; FL: flavonoids.