4.7 Article

Influence of side chain structure changes on antioxidant potency of the [6]-gingerol related compounds

Journal

FOOD CHEMISTRY
Volume 165, Issue -, Pages 191-197

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2014.05.077

Keywords

Gingerol; Shogaol; Antioxidant; DNA damage; Lipid peroxidation

Funding

  1. National Natural Science Foundation of China [31100607]
  2. Fundamental Research Funds for the Central Universities [lzujbky-2013-52]

Ask authors/readers for more resources

161-Gingerol and [6]-shogaol are the major pungent components in ginger with a variety of biological activities including antioxidant activity. To explore their structure determinants for antioxidant activity, we synthesized eight compounds differentiated by their side chains which are characteristic of the C-1-C-2 double bond, the C-4-C-5 double bond or the 5-OH, and the six- or twelve-carbon unbranched alkyl chain. Our results show that their antioxidant activity depends significantly on the side chain structure, the reaction mediums and substrates. Noticeably, existence of the 5-OH decreases their formal hydrogen-transfer and electron-donating abilities, but increases their DNA damage- and lipid peroxidation-protecting abilities. Additionally, despite significantly reducing their DNA strand breakage-inhibiting activity, extension of the chain length from six to twelve carbons enhances their anti-haemolysis activity. (C) 2014 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available