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. 2021 Jul 14;366:130589. doi: 10.1016/j.foodchem.2021.130589

Table 2.

List of compounds used in this study.

Compound name ID
Quinic acid 1
Hesperetin-7-O-(rhamnoside, glucoside)-glucoside 2
Hesperetin (*) 3
Dimethoxycinnamoylhexoside 4
Ferulic acid (*) 5
5-O-cafeoylquinic acid 6
Luteolin-3′,7-di-O-glucoside 7
Myricetin glucuronide 8
Methylmyricetin-O-glucuronide 9
Vicenin-2 10
Myricetin rhamno-hexoside 11
Myricetin (*) 12
Quercetin 3-O-(2, 6-di-orhamnosyl-glucoside) 13
Luteolin 6,8-di-C-hexoside 14
Luteolin 15
Avicularin 16
Pinoquercetin 17
Quercetin 18
Quercetin-3-O-arabinoglucoside 19
Apigenin 6,8-di-C-glucoside (vicenin-3) 20
Apigenin (*) 21
Quercetin-O-rutinoside 22
Quercetin-3-glucuronide 23
Quercetin-3-galactoside-6′'-rhamnoside-3′''-rhamnoside 24
Dihydroxy-methoxyflavanone-O-rutinoside 25
5,7-dihydroxy-4′-methoxyflavanone (*) 26
Kaempferol-3-O-glucoside 27
Kaempferol-3-O-glucuronide 28
Kaempferol (*) 29
Isorhamnetin-3-O-(6-O-rhamnosyl-galactoside) 30
Isorhamnetin (*) 31
Isorhamnetin-3-O-glucoside-6-O-rhamnoside 32
2-(3,4-dihydroxyphenyl)-3,5,6-trihydroxychromen-4-one (*) 33
Sennoside 34
Baicalin 35
Hydroxyhein-O-rhamnoside–glucoside 36
Rhein (*) 37
Sagerinic acid 38
Caffeic acid trimer 39
(2S,3S,4S,5R,6S)-6-[2-(3,4- Dihydroxyphenyl)-5- hydroxy-4-oxochromen-7- yl]oxy-3,4,5- trihydroxyoxane-2- carboxylic acid 40
Lithospermic acid 41
Triterpene acid-O-hexoside 42
(Epi)gallocatechin (**) 43
(Epi)catechin dimer (**) 44
Benzenebutanoic acid, 4-methoxy-, methyl ester (***) 45
l-Leucine, N-isobutoxycarbonyl-N-methyl-, heptyl ester (***) 46
7-Acetyl-6-ethyl-1,1,4,4-tetramethyltetralin (***) 47
Benzoic acid, 2-(ethylthio)-, ethyl ester (***) 48
Undecanoic acid, trimethylsilyl ester (***) 49
1H-.beta.-Carboline-3-carboxylic acid, 1-isopropyl-2,3,4,9-tetrahydro-, methyl ester (***) 50
Isopeucenin (***) 51

Note: (*) Because it is possible the hydrolysis of the glycoside part of several of those molecules (especially in the acidic gastric environment), we decided to include also the molecules free from the glyosidic portion of the molecule. (**) The original tentative identification was (Guevara et al., 2020): (Epi)gallocatechin-(epi)catechin dimer. Following the same logic both molecules were considered separately. (***) Molecules identified by GC–MS analysis.