Chemical studies of the antioxidant mechanism of theaflavins:: radical reaction products of theaflavin 3,3′-digallate with hydrogen peroxide

被引:11
作者
Sang, SM
Tian, SY
Jhoo, JW
Wang, H
Stark, RE
Rosen, RT
Yang, CS
Ho, CT
机构
[1] Rutgers State Univ, Dept Food Sci, New Brunswick, NJ 08901 USA
[2] Rutgers State Univ, Ctr Adv Food Technol, New Brunswick, NJ 08901 USA
[3] CUNY Coll Staten Isl, Staten Isl, NY 10314 USA
[4] Grad Ctr, Dept Chem, Staten Isl, NY 10314 USA
[5] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Biol Chem, Piscataway, NJ 08854 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0040-4039(03)01382-0
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The objective of the current study is to characterize the reaction products of theaflavin 3,3'-digallate, one of the major characteristic polyphenols of black tea, with hydroxyl radicals generated by hydrogen peroxide, with the aim of gaining insights into specific mechanisms of antioxidant reactions in physiological systems. Two major reaction products were isolated and identified using high-field 1D and 2D NMR spectral analysis. Both of them are A-ring fission products. The observation of these compounds indicates that the A ring rather than the benzotropolone moiety is the initial site for formation of reaction products in the hydrogen peroxide oxidant system. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5583 / 5587
页数:5
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