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Hydroxyl radical generation via photoreduction of a simple pyridine N-oxide by an NADH analogue
Authors:Nakanishi Ikuo  Nishizawa Chiho  Ohkubo Kei  Takeshita Keizo  Suzuki Kazuo T  Ozawa Toshihiko  Hecht Sidney M  Tanno Masayuki  Sueyoshi Shoko  Miyata Naoki  Okuda Haruhiro  Fukuzumi Shunichi  Ikota Nobuo  Fukuhara Kiyoshi
Institution:Redox Regulation Research Group, Research Center for Radiation Safety, National Institute of Radiological Sciences (NIRS), Inage-ku, Chiba, 263-8555, Japan. nakanis@nirs.go.jp
Abstract:Photoreduction of pyridine N-oxide, which has a key structure of antitumor agents for hypoxic solid tumors, by 1-benzyl-1,4-dihydronicotinamide in deaerated aprotic media resulted in generation of hydroxyl radical, leading to the oxidation of salicylic acid to 2,3- and 2,5-dihydroxybenzoic acids, and catechol.
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