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. 2022 Apr 4;9:882458. doi: 10.3389/fnut.2022.882458

Table 1.

Phenolic compounds analyzed in this study (phenolic acids and subgroups of flavonoids) along with reference standard names, sample codes and substituents (reproduced and slightly modified from this table in Platzer et al. (11, 14)).

Subgroups Reference standards Code Position and substituents
Phenolic acids 1 3 4 5
Caffeic acid CAA (CH2)2COOH OH OH H
3,4-dihydroxybenzoic acid DBA COOH OH OH H
Ferulic acid FEA (CH2)2COOH OCH3 OH H
Gallic acid GAA COOH OH OH OH
4-hydroxybencoic acid HBA COOH H OH H
p-coumaric acid PCA (CH2)2COOH H OH H
Sinapic acid SIA (CH2)2COOH OCH3 OH OCH3
Syringic acid SRA COOH OCH3 OH OCH3
Flavonols 2' 3' 4' 5' 3 5 7
Isorhamnetin IRT H OCH3 OH H OH OH OH
Kaempferol KAE H H OH H OH OH OH
Morin MOR OH H OH H OH OH OH
Myricetin MYR H OH OH OH OH OH OH
Quercetin-3-D-glucoside QGU3 H OH OH H Gal OH OH
Quercetin-7-D-glucoside QGU7 H OH OH H OH OH Glc
Quercetin QUR H OH OH H OH OH OH
Flavanones 3' 4' 3 5 7
Hesperetin HES OH OCH3 H OH OH
Narirutin NAR H OH H OH 2 Glc
Naringin NAG H OH H OH Rham, Glc
Naringenin NAN H OH H OH OH
Taxifolin TAF OH OH OH OH OH
Dihydrochalcones 4 2' 4' 6'
Phloridzin PHD OH OH OH Glc
Phloretin PHT OH OH OH OH
Flavanols 3' 4' 3 4 5 7
(+)-catechin CAT OH OH OH H OH OH
(−)-epicatechin EPC OH OH OH H OH OH