Development of novel nitroxyl radicals for controlling reactivity with ascorbic acid

Yuichi Kinoshita, Ken Ichi Yamada, Toshihide Yamasaki, Hiromi Sadasue, Kiyoshi Sakai, Hideo Utsumi

研究成果: ジャーナルへの寄稿学術誌査読

44 被引用数 (Scopus)

抄録

Piperidine and pyrrolidine nitroxyl radicals (nitroxide) contain unpaired electrons and have been widely recognized as antioxidants, contrast agents, spin probes, radiation protective agents and polymerization mediators. Nitroxyl radicals can react with free radicals and reductants and their reactivities depend on the basic structure of the nitroxyl radicals themselves. However, reductants easily reduce these radicals and they lose their paramagnetic nature and function. Therefore, the aim of this study was to develop various functional nitroxyl radicals, particularly focusing on stability towards AsA through the improvement of the synthetic route for a series of 2,6-substituted nitroxyl radicals. Tetraethyl-substituted piperidine nitroxyl radical 8 exhibited resistance to AsA reduction and 2,6-dispiro-4′,4″-dipyrane-piperidin-4-one-N-oxyl 5 had a second-order rate constant 10-times greater than those of hydroxyl-TEMPO and oxo-TEMPO. The 2,6-substituted compound offers various reactivities towards AsA and the possibility to be used as a new antioxidant, contrast agent and radical polymerizer.

本文言語英語
ページ(範囲)565-571
ページ数7
ジャーナルFree Radical Research
43
6
DOI
出版ステータス出版済み - 2009

!!!All Science Journal Classification (ASJC) codes

  • 生化学

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