Voltammetric and Spectroscopic Studies on the Carcinogen 4-(Hydroxyamino)quinoline N-Oxide and Its Analogues(Physical,Chemical)
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概要
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In connection with the carcinogenic activity of 4-(hydroxyamino)quinoline N-oxide (4HAQO), voltammetric studies of the oxidation processes of 4HAQO and related substances were carried out in aqueous solutions. It was verified that 4HAQO forms a reversible redox couple with 4-nitrosoquinoline N-oxide (4NOQO) through an intermediate free radical. The reversible reactions in these redox couples were evaluated quantitatively, and the formation constant of the intermediate free radical was calculated. The pH dependence of the above standard redox potential gave the pK_a values, which agreed quite well with the data measured by ultraviolet spectral methods. The molecular structures of species formed by proton addition or dissociation were investigated by analyses of the pK_a values and the electronic spectra, and by their molecular orbital calculations. The N-oxide type structure was considered to be a main species in aqueous solutions of 4HAQO and its analogues.
- 公益社団法人日本薬学会の論文
- 1987-05-25
著者
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加納 健司
京大農
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川添 豊
Faculty of Pharmaceutical Sciences, Nagoya City University
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高橋 和彦
横浜薬科大学
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高橋 和彦
Faculty of Pharmaceutical Sciences, Nagoya City University
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川添 豊
Faculty Of Pharmaceutical Sciences Nagoya City University
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高橋 和彦
名市大 院
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窪田 種一
岐阜薬科大学
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高橋 和彦
Faculty Of Pharmaceutical Sciences Nagoya City University
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張 正行
Glfu Pharmaceutical University
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改田 直樹
Gifu Pharmaceutical University
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加納 健司
Glfu Pharmaceutical University
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宇野 文二
Glfu Pharmaceutical University
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改田 直樹
Glfu Pharmaceutical University
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窪田 種一
Glfu Pharmaceutical University
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高橋 和彦
Faculty of Agriculture, Department of Horticulture, University of Tokyo
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