SYNTHESIS OF 5-FLUOROARACHIDONIC ACID AND ITS BIOTRANSFORMATION TO 5-FLUORO-12-HYDROXYEICOSATETRAENOIC ACID(Communications to the Editor)
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概要
- 論文の詳細を見る
The synthesis of 5-fluoroarachidonic acid (1) was achieved from the intermediate (E)-5, 6-dihydroxy-2-fluorohex-2-enoate 5, 6-acetonide (5). Incubation of 1 with human platelets yielded 5-fluoro-12-hydroxyeicosatetraenoic acid (5F-12-HETE, 2).
- 公益社団法人日本薬学会の論文
- 1987-04-25
著者
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田中 洋子
ベテランズ・アフェアーズ・メディカルセンター
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田口 武夫
東京薬科大学薬学部
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小林 義郎
Tokyo College of Pharmacy
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田口 武夫
Tokyo College of Pharmacy
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小林 義郎
東京薬科大学薬学部
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Taguchi T
Department Of Pathobiochemistry Faculty Of Pharmacy Meijo University
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瀧川 智之
Tokyo College of Pharmacy
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五十嵐 東
Tokyo College of Pharmacy
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田中 洋子
Veterans Administration Medical Center and Department of Medicine, Albany Medical College
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Jubiz William
Veterans Administration Medical Center and Department of Medicine, Albany Medical College
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Briggs Robert
Wadsworth Center for Laboratories and Research, New York State Department of Health
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Briggs Robert
Wadsworth Center For Laboratories And Research New York State Department Of Health
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Jubiz William
Veterans Administration Medical Center And Department Of Medicine Albany Medical College
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