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. 2022 Feb 17;13:100258. doi: 10.1016/j.fochx.2022.100258

Table 1.

Phenolic compounds found in C. japonica extracts, identification from different plant parts and associated bioactivities (Center, 2020).

Compounds Identification Part Associated bioactivities Refs.
Phenolic acids
Gallic acid GC–MS L, P, F Antimicrobial, anti-inflammatory, antioxidant, anticancer (Kanth et al., 2014, Lee et al., 2005, Lee et al., 2016, Moon and Kim, 2018)
p-hydroxybenzoic acid HPLC F Antioxidant, antimicrobial (Nakajima, Itokawa, & Ikuta, 1984)
3,4,5-trihydroxybenzoic acid, 3,4-dihydroxybenzoic acid, 4-hydroxybenzoic acid, 2,3-digalloyl-O-α-d-glucopyranoside, and 2,3-digalloyl-O-β-d-glucopyranoside NMR, HPLC F Antioxidant (Lee, Cho, Moon, & Park, 2011)



Flavonoids
Quercetin GC–MS L, F Antimicrobial, anti-inflammatory, anticancer, antioxidant (Kim, Jeong, & Shim, 2010, Lee et al., 2016, Moon and Kim, 2018, Piao et al., 2011)
Quercetin 3-O-β-d-galactopyranoside, quercetin 3-O-β-d-glucopyranoside NMR, GC–MS F, L Antioxidant, anti-hyperuricemia (Lee et al., 2011, Yoon et al., 2017)
Camellianoside HPLC L Antioxidant, antiviral (Onodera et al., 2006, Park et al., 2002)
Epicatechin GC–MS L, F Antimicrobial, anti-inflammatory, anticancer, antioxidant (Kim et al., 2010; Lee et al., 2016, Moon and Kim, 2018, Piao et al., 2011)
Kaempferol HPLC F Antioxidant, anti-inflammatory, antimicrobial, anticancer, cardioprotective, neuroprotective, anti-diabetes (Nakajima et al., 1984)
Kaempferol 3-O-β-d-galactopyranoside and kaempferol 3-O-β-d-glucopyranoside NMR, GC–MS F, L Antioxidant, anti-hyperuricemia (Lee et al., 2011, Yoon et al., 2017)
Kaempferol-3-O-β-d-xylopyranosyl(1 → 3)-α-l-rhamnopyranosyl(1 → 6)-O-β-d-galactopyranoside, kaempferol-3-O-α-l-rhamnopyranosyl-(1 → 6)-O-β-d-xylopyranosyl-(1 → 2)-O-β-d-galactopyranoside, kaempferol-3-O-β-d-xylopyranosyl-(1 → 3)-O-α-l-rhamnopyranosyl-(1 → 6)-O-β-d-glucopyranosyl-(1 → 2)-O-β-d-gluctopyranoside, tsubakiosides A-D, camelliaside B HPLC-PDA S Antioxidant, anti-aging (Ko et al., 2020)
Sexangularetin HPLC F Antioxidant, anti-inflammatory, antimicrobial, anticancer (Nakajima et al., 1984)
Anthocyanidins: cyanidin 3-O-(6-O-(E)-p-coumaroyl)-β-glucopyranoside, cyanidin 3-O-(6-O-(E)-p-coumaroyl)-β-galactopyranoside, cyanidin 3-O-(6-O-(E)-caffeoyl)-β-glucopyranoside, cyanidin 3-O-(6-O-(E)-caffeoyl)-β-galactopyranoside HPLC F Antioxidant (Li et al., 2009)



Tannins
Camelliatannins A, B, C, H NMR L Antiviral (Yang et al., 2015)
Camelliatannins D, F, G NMR L Antiviral (Han et al., 1994, Hatano et al., 1991, Hatano et al., 1995)
Camelliins A and B NMR F Antiviral (Yoshida et al., 1990)

Description. GC–MS: gas chromatography-mass spectrometry analysis; HPLC: high-performance liquid chromatography; NMR: nuclear magnetic resonance spectroscopy; TLC: thin-layer chromatography; HPLC-PDA: high-performance liquid chromatography coupled to photodiode array detector; // L: leaves; F: flowers; S: seeds; P: fruit peels.