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Radical-scavenging and antioxidant activity of avenanthramides
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Kemiska institutionen, Avdelningen för organisk kemi.
2009 (Engelska)Ingår i: Food Chemistry, ISSN 0308-8146, E-ISSN 1873-7072, Vol. 113, nr 2, s. 550-556Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Avenanthramides are amides of cinnamoyl-anthranilic acids and, among cereals, are exclusively found in oats. This study investigated the structure-antioxidant activities of 15 avenanthramides with different substitution patterns in the two aromatic rings, seven of which were new avenanthramides synthesised and characterised in this study. Radical-scavenging activity was tested as reactivity towards 1,1-diphenyl-2-picrylhydrazyl (DPPH-). The activity increased with the number of radical-stabilising groups ortho to the phenolic hydroxy group. Both aromatic rings were independently important for activity, while conjugation across the amide bond was of minor importance. Antioxidant activity was determined as inhibition of linoleic acid oxidation. In contrast to the radical-scavenging activity, antioxidant activity was observed for most avenanthramides, and also for compounds with only one hydroxy group in either of the aromatic rings. Compared with alpha-tocopherol, the avenanthramides protected linoleic acid from oxidation to a smaller extent initially, but the effect lasted for a longer time.

Ort, förlag, år, upplaga, sidor
2009. Vol. 113, nr 2, s. 550-556
Nyckelord [en]
1, 1-Diphenyl-2-picrylhydrazyl, Antioxidants, Avenanthramides, DPPH, Linoleic acid, Oats
Nationell ämneskategori
Annan medicinsk grundvetenskap
Identifikatorer
URN: urn:nbn:se:uu:diva-107034DOI: 10.1016/j.foodchem.2008.07.101ISI: 000261084600027OAI: oai:DiVA.org:uu-107034DiVA, id: diva2:227586
Tillgänglig från: 2009-07-15 Skapad: 2009-07-15 Senast uppdaterad: 2018-01-13Bibliografiskt granskad

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