| Literature DB >> 31888242 |
Oana-Crina Bujor1, Corneliu Tanase2, Mona Elena Popa3.
Abstract
Phenolic compounds are a widespread group of secondary metabolites found in all plants, representing the most desirable antioxidants due to their potential to be used as additives in the food industry (inhibition of lipid oxidation), and in cosmetology and medicine (protection against oxidative stress). In recent years, demand for the identification of edible sources rich in phenolic antioxidants, as well as the development of new natural plant products to be used as dietary supplements or pharmaceuticals, has been a great preoccupation. At present, from the "circular economy" perspective, there is an increased interest to use agricultural waste resources to produce high-value compounds. Vaccinium leaves and stems are considered essentially an agro-waste of the berry industry. Scientific studies have shown that phenolic compounds were found in a markedly higher content in the leaves and stems of Vaccinium plants than in the fruits, in agreement with the strongest biological and antioxidant activities displayed by these aerial parts compared to fruits. This paper aims to review the current state of the art regarding the phenolic antioxidants from leaves and stems of two wild Vaccinium species, bilberry (Vaccinium myrtillus L.) and lingonberry (Vaccinium vitis-idaea L.), as promising natural resources with pharmaceutical and biological activity.Entities:
Keywords: Vaccinium; antioxidants; leaves; natural resources; pharmaceutical products; polyphenols; stems
Year: 2019 PMID: 31888242 PMCID: PMC6943522 DOI: 10.3390/antiox8120649
Source DB: PubMed Journal: Antioxidants (Basel) ISSN: 2076-3921
Phenolic compounds identified in aerial parts of Vaccinium plants.
| Class | Phenolic Compounds |
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| References | ||
|---|---|---|---|---|---|---|
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| Catechins | (+)-catechin | x | x | x | x | [ |
| (−)-epicatechin | x | x | x | x | [ | |
| gallocatechin | x | x | - | x | [ | |
| epigallocatechin | x | x | - | x | ||
| Cinchonains | cinchonain I | x | x | x | x | [ |
| cinchonain II | x | x | x | x | ||
| Proanthocyanidins | B-type dimer | x | x | x | x | [ |
| B-type trimer | x | x | x | x | ||
| B-type tetramer | x | x | x | x | [ | |
| B-type pentamer | x | x | - | - | ||
| A- type dimer | x | x | x | x | [ | |
| A-type trimer | x | x | x | x | [ | |
| procyanidin A2 | x | x | x | x | ||
| procyanidin B1 | x | x | x | x | ||
| procyanidin B2 | x | x | x | x | ||
| Arbutin derivatives | arbutin | - | - | x | x | [ |
| caffeoyl acetyl arbutin | - | - | x | - | [ | |
| caffeoyl arbutin | - | - | x | - | [ | |
| acetyl arbutin | - | - | x | x | [ | |
| Phenolic acids | 3,4-dihydroxybenzoic acid | x | x | x | x | [ |
| x | x | x | x | |||
| x | x | x | x | |||
| x | x | x | x | |||
| coumaroyl iridoid | x | x | - | - | ||
| x | - | x | - | [ | ||
| feruloyl quinic acid isomer | x | - | x | - | ||
| caffeoyl quinic acid isomers | x | - | x | - | ||
| caffeic acid ethyl ester | x | - | x | - | ||
| caffeic acid hexoside | x | - | x | - | ||
| Flavonols | quercetin-3- | x | x | x | x | [ |
| quercetin-3- | x | x | x | x | ||
| quercetin-3- | x | x | x | x | ||
| quercetin-3- | x | x | x | x | ||
| quercetin-3- | x | x | x | x | ||
| quercetin-3- | x | x | x | x | ||
| quercetin-3- | x | x | x | x | ||
| quercetin | - | - | x | x | [ | |
| kaempferol | x | - | x | - | [ | |
| kaempferol-hexoside | x | - | x | - | [ | |
| kaempferol-(HMG)-rhamnoside | x | - | x | - | ||
| kaempferol- | x | - | x | - | ||
| kaempferol-3-glucuronide | x | - | - | - | [ | |
| Lignans | Lyoniside (9- | - | x | - | - | [ |
x, present; -, not present.