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  Carotenylflavonoids, a novel group of potent, dual-functional antioxidants

Beutner, S., Frixel, S., Ernst, H., Hoffmann, T., Hernandez-Blanco, I., Hundsdoerfer, C., et al. (2007). Carotenylflavonoids, a novel group of potent, dual-functional antioxidants. ARKIVOC, (8), 279-295. doi:10.3998/ark.5550190.0008.822.

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 Creators:
Beutner, Stefan1, Author
Frixel, Susanne1, Author
Ernst, Hansgeorg2, Author
Hoffmann, Thomas1, Author
Hernandez-Blanco, Ines1, Author
Hundsdoerfer, Claas1, Author
Kiesendahl, Nicole1, Author
Kock, Sebastian1, Author
Martin, Hans-Dieter1, Author
Mayer, Bernhard1, Author
Noack, Peter1, Author
Perez-Galvez, Antonio3, Author
Kock, Grit1, Author
Scherrers, Roger1, Author
Schrader, Wolfgang4, Author           
Sell, Stefan1, Author
Stahl, Wilhelm1, Author
Affiliations:
1University of Duesseldorf, Universitaetsstr. 1, D-40225 Duesseldorf, Germany, ou_persistent22              
2BASF AG, Germany, ou_persistent22              
3Instituto de la Grasa (CSIC), Sevilla, Spain, ou_persistent22              
4Service Department Schrader (MS), Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445629              

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Free keywords: carotenoids; flavonoids; carotenylflavonoids; antioxidants; peroxide inhibition
 Abstract: We report here on the synthesis and antioxidant properties of novel covalently linked flavonoidcarotenoid
hybrids, hereinafter referred to as carotenylflavonoids. By this strategy the essential
properties of the protecting systems are improved. Compared with the parent carotenoids or flavonoids,
e.g. ß-carotene and a hydroxyflavone, these molecular combinations exhibit improved
photoprotective properties, as seen from their UV spectra, and they outperform the individual
constituents in their antioxidant properties. The dual functionality is revealed from the time evolution
of the peroxidation inhibition assay which clearly displays both phenolic and carotenoidpolyenic
contributions to the antioxidant efficiency. Furthermore, these compounds have amphiphilic
character, in contrast to symmetrical carotenes and hydroxylated flavones. The antioxidative
potential of the carotenylflavonoids is high. They protect cumene against peroxidation
more than β-carotene by a factor of about 2.3-2.5, and more than the individual components.

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Language(s): eng - English
 Dates: 2006-11-272007-01-102007-01-23
 Publication Status: Issued
 Pages: 17
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.3998/ark.5550190.0008.822
 Degree: -

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Title: ARKIVOC
  Other : Arkivoc
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Zürich : ARKAT
Pages: - Volume / Issue: (8) Sequence Number: - Start / End Page: 279 - 295 Identifier: ISSN: 1424-6376
CoNE: https://pure.mpg.de/cone/journals/resource/111006902711068