Stereochemistry of Hydrogen Addition to C-25 of Desmosterol by Sterol-Δ^<24>-Reductase of Rat Liver Homogenate
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概要
- 論文の詳細を見る
Chemically synthesized (26)- and (27)-methyl-^<13>C-labeled desmosterol (3,5) were separately incubated with rat liver homogenate. ^<13>C-NMR analysis of the incubation products indicated that the C-25 hydrogen of cholesterol was introduced from the si-face of 3 and the re-face of 5.
- 社団法人日本薬学会の論文
- 1994-03-15
著者
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小林 典子
共立薬大
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森崎 益雄
共立薬大
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小林 典子
Kyoritsu College of Pharmacy
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森崎 益雄
Kyoritsu College of Pharmacy
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藤本 善徳
Department of Chemistry, Tokyo Institute of Technology
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八木 知子
Kyoritsu College of Pharmacy
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原 典行
Department of Chemistry, Tokyo Institute of Technology
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藤本 善徳
東工大院理工
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藤本 善徳
Department Of Chemistry Tokyo Institute Of Technology
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原 典行
東工大院理工
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原 典行
Department Of Chemistry Tokyo Institute Of Technology
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