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The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Structure−Activity Relationships of Flavonoids in the Cellular Antioxidant Activity Assay

Wolfe, Kelly L., Liu, Rui Hai·2008·Journal of Agricultural and Food Chemistry

Abstract

Chemical antioxidant activity assays are used extensively to evaluate the potential bioactivity of plant foods and their phytochemical constituents, but they do not mimic the complexity of biological systems. The cellular antioxidant activity (CAA) activity assay was developed to be a more biologically relevant model to measure antioxidant activity. Structure-activity relationships of flavonoids have been determined in many chemistry antioxidant activity assays, and they vary with the protocols. The objective of this study was to determine structure-activity relationships of selected flavonoids in the CAA assay. The structures that conferred flavonoids with the most antioxidant activity in the CAA assay were a 3',4'- o-dihydroxyl group in the B-ring, a 2,3-double bond combined with a 4-keto group in the C-ring, and a 3-hydroxyl group. Isoflavones had no cellular antioxidant activity. Flavanols with a galloyl moiety had higher antioxidant activity than those without, and a B-ring 3',4',5'-trihydroxyl group further improved their efficacy. ORAC values for flavonoids were not related to their CAA values. Knowledge of structure-activity relationships in the CAA assay may be helpful in assessing potential in vivo antioxidant activity of flavonoids.

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Metadata

Authors
Wolfe, K. L., & Liu, R. H.
Venue
Journal of Agricultural and Food Chemistry
Published
2008-08-15
Volume
56
Issue
18
Pages
8404-8411
ISSN
  • 0021-8561 (ISSN-L)
  • 1520-5118
OpenAlex
W1972510752
Cited by
392
References
4
FWCI
9.83
Type
journal article
Language
en
Open access
closed

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