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Pro- and Antioxidant Activity of Three Selected Flavan Type Flavonoids: Catechin, Eriodictyol and Taxifolin

The flavanol (±)-catechin shows an OH group but no 4-keto group on ring C (C3), and no conjugation between ring A and B. The related flavanone (+)-eriodictyol has a keto group on C4 but no 3-OH group on ring C. (+)-Taxifolin, another flavanone, has an OH on C3 and a keto group on C4 of the C ring. D...

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Autores principales: Chobot, Vladimir, Hadacek, Franz, Bachmann, Gert, Weckwerth, Wolfram, Kubicova, Lenka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5187786/
https://www.ncbi.nlm.nih.gov/pubmed/27898046
http://dx.doi.org/10.3390/ijms17121986
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author Chobot, Vladimir
Hadacek, Franz
Bachmann, Gert
Weckwerth, Wolfram
Kubicova, Lenka
author_facet Chobot, Vladimir
Hadacek, Franz
Bachmann, Gert
Weckwerth, Wolfram
Kubicova, Lenka
author_sort Chobot, Vladimir
collection PubMed
description The flavanol (±)-catechin shows an OH group but no 4-keto group on ring C (C3), and no conjugation between ring A and B. The related flavanone (+)-eriodictyol has a keto group on C4 but no 3-OH group on ring C. (+)-Taxifolin, another flavanone, has an OH on C3 and a keto group on C4 of the C ring. Deoxyribose degradation assay systems, with hydrogen peroxide and ascorbic acid either added or omitted, were performed in variants in which Fe(III) was added in a complex with ethylenediaminetetraacetic acid (EDTA). In combination with differential pulse voltammetry (DVP), the specific redox-chemical contributions of the ring A m-dihydroxyl groups could be explored more specifically in addition to those of the traditionally investigated o-dihydroxyl groups of ring B.
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spelling pubmed-51877862016-12-30 Pro- and Antioxidant Activity of Three Selected Flavan Type Flavonoids: Catechin, Eriodictyol and Taxifolin Chobot, Vladimir Hadacek, Franz Bachmann, Gert Weckwerth, Wolfram Kubicova, Lenka Int J Mol Sci Article The flavanol (±)-catechin shows an OH group but no 4-keto group on ring C (C3), and no conjugation between ring A and B. The related flavanone (+)-eriodictyol has a keto group on C4 but no 3-OH group on ring C. (+)-Taxifolin, another flavanone, has an OH on C3 and a keto group on C4 of the C ring. Deoxyribose degradation assay systems, with hydrogen peroxide and ascorbic acid either added or omitted, were performed in variants in which Fe(III) was added in a complex with ethylenediaminetetraacetic acid (EDTA). In combination with differential pulse voltammetry (DVP), the specific redox-chemical contributions of the ring A m-dihydroxyl groups could be explored more specifically in addition to those of the traditionally investigated o-dihydroxyl groups of ring B. MDPI 2016-11-26 /pmc/articles/PMC5187786/ /pubmed/27898046 http://dx.doi.org/10.3390/ijms17121986 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chobot, Vladimir
Hadacek, Franz
Bachmann, Gert
Weckwerth, Wolfram
Kubicova, Lenka
Pro- and Antioxidant Activity of Three Selected Flavan Type Flavonoids: Catechin, Eriodictyol and Taxifolin
title Pro- and Antioxidant Activity of Three Selected Flavan Type Flavonoids: Catechin, Eriodictyol and Taxifolin
title_full Pro- and Antioxidant Activity of Three Selected Flavan Type Flavonoids: Catechin, Eriodictyol and Taxifolin
title_fullStr Pro- and Antioxidant Activity of Three Selected Flavan Type Flavonoids: Catechin, Eriodictyol and Taxifolin
title_full_unstemmed Pro- and Antioxidant Activity of Three Selected Flavan Type Flavonoids: Catechin, Eriodictyol and Taxifolin
title_short Pro- and Antioxidant Activity of Three Selected Flavan Type Flavonoids: Catechin, Eriodictyol and Taxifolin
title_sort pro- and antioxidant activity of three selected flavan type flavonoids: catechin, eriodictyol and taxifolin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5187786/
https://www.ncbi.nlm.nih.gov/pubmed/27898046
http://dx.doi.org/10.3390/ijms17121986
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