Abstract
Procyanidins B-l and B-3 from azuki beans showed remarkable scavenging activities, especially to hydrophilic radicals. The inhibition rate constants for the scavenging of hydrophilic peroxyl radicals generated from 2, 2′-azobis(2-amidinopropane)hydrochloride in aqueous media were calculated at 37°C to be kinh = 6.0×104M-1s-1, 5.9×104M-1s-1, 2.7×104M-1s-1, 5.0×104M-1s-1 and 1.1 × 105M-1s-1, and the stoichiometric factors as n=8.4, 8.0, 3.7, 1.2 and 1.7 for procyanidin B-1, procyanidin B-3, (+)-catechin, ascorbic acid and α-tocopherol, respectively. Thus, the dimeric procyanidin molecule could trap eight radicals. The production and structures of procyanidin B-3 radicals are discussed on the basis of the ESR spectra observed by autoxidation of procyanidin B-3 in an aqueous alkaline methanol solution. © 1990, Japan Society for Bioscience, Biotechnology, and Agrochemistry. All rights reserved.
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CITATION STYLE
Ariga, T., & Hamano, M. (1990). Antioxidative properties of proanthocyanidins. Part II. Radical scavenging action and its mode in procyanidins B-1 and B-3 from azuki beans to peroxyl radicals. Agricultural and Biological Chemistry, 54(10), 2499–2504. https://doi.org/10.1271/bbb1961.54.2499
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