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The high stability of intermediate radicals enhances the radical-scavenging activity of aminochromanols

Title
The high stability of intermediate radicals enhances the radical-scavenging activity of aminochromanols
Authors
Inami K.Nakanishi I.Morita M.Furukawa M.Ohkubo K.Fukuzumi S.Mochizuki M.
Ewha Authors
Shunichi Fukuzumi
SCOPUS Author ID
Shunichi Fukuzumiscopus
Issue Date
2012
Journal Title
RSC Advances
ISSN
2046-2069JCR Link
Citation
vol. 2, no. 33, pp. 12714 - 12717
Indexed
SCIE; SCOPUS WOS scopus
Abstract
The hydroxyl radical-scavenging activity of the amino-substituted α-tocopherol analogues was much higher than that of α-tocopherol. Aminochromanoxyl radicals generated from 5- and 7-aminochromanol were successfully detected in aqueous solution at room temperature during ESR measurements. The stability of the aminochromanoxyl radicals leads to a significant enhancement of the radical-scavenging activity. © 2012 The Royal Society of Chemistry.
DOI
10.1039/c2ra21928j
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자연과학대학 > 화학·나노과학전공 > Journal papers
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