REDUCTION OF METHYL 5-NITRO-2-FUROATE BY XANTHINE OXIDASE : AN EVIDENCE FOR HYDROXYLAMINOFURAN FORMATION
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概要
- 論文の詳細を見る
After methyl 5-nitro-2-furoate was incubated with milk xanthine oxidase, two reduction products were isolated from the incubation mixture. Metabolite 1 was positive to a pentacyanoammineferroate reagent and data obtained from mass spectrometry of its acetylated derivative indicated that the metabolite was the hydroxylaminofuran derivative (methyl 5-hydroxylamino-2-furoate). Metabolite 2 was identified as the aminofuran derivative (methyl 5-amino-2-furoate) by comparison with a synthetic sample.
- 社団法人日本薬学会の論文
- 1982-07-25
著者
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辰巳 淳
Institute of Pharmaceutical Sciences, Faculty of Medicine, Kyushu University
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山田 英之
九州大学薬学部
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山田 英之
九州大学 院 薬
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辰巳 淳
Institute Of Pharmaceutical Sciences Hiroshima University School Of Medicine
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吉村 英敏
中村学園大・食物栄養
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吉村 英敏
Faculty Of Pharmaceutical Sciences Kyushu University
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山田 英之
Faculty of Pharmaceutical Sciences, Kyushu University 62
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Yoshimura Hidetoshi
Department Of Food And Nutrition Nakamura Gakuen University
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辰巳 淳
Institute of pharmaceutical Sciences, Hiroshima University School of Medicine
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