| Literature DB >> 10861967 |
H Y Choi1, E J Jhun, B O Lim, I M Chung, S H Kyung, D K Park.
Abstract
Chemiluminescence (CL) was observed during the oxidation of luminol (2 mg/L). mediated by 0.06% hydrogen peroxide (H(2)O(2)) and cytochrome c (10 mg/L). CL intensity was decreased by the presence of radical scavengers and the reduction was linearly proportional to the concentration and ability of scavengers; butylated hydroxytoluene (BHT), caffeic acid and gallic acid. The order of effectiveness as radical scavengers was gallic acid > caffeic acid > BHT, which shows that the number of hydroxyl groups (OH) in the B-ring of flavonoids plays a key role in a good radical scavenging activity. Of eight catechins obtained from green tea extracts, (-)-catechin was the least effective and (-)-epigallocatechin gallate (EGCg) showed the strongest activity. This result indicates that the stereoscopic structure between the C-3 group and the B ring of flavonoids as well as substituents at the C-3 position make a contribution to radical scavenging activity. Of the tested Chinese herbal ingredients, five species of ingredients represented more than 90% of the radical scavenging activity. Copyright 2000 John Wiley & Sons, Ltd.Entities:
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Year: 2000 PMID: 10861967 DOI: 10.1002/1099-1573(200006)14:4<250::aid-ptr587>3.0.co;2-j
Source DB: PubMed Journal: Phytother Res ISSN: 0951-418X Impact factor: 5.878