α-Glucosidase Inhibitors with a Phthalimide Skeleton : Stucture-Activity Relationship Study
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概要
- 論文の詳細を見る
α-Glucosidase inhibitors with a phthalimide skeleton were prepared. Structure-activity relationship studies indicated a critical role for the hydrophobicity of the substituent at the nitrogen atom of the phthalimide skeleton. Introduction of electron-withdrawing groups, including a nitro group and chlorine, influenced the activity.Optimization studies led us to design 4,5,6,7-tetrachloro-N-phenylphthalimide (CP0P) and its N-phenylalkyl derivatives. CP0P and 4,5,6,7-tetrachloro-N-(4-phenylbutyl)phthalimide (CP4P) proved to be more potent α-glucosidase inhibitors than the known inhibitor 1-deoxynojirimycin.
- 公益社団法人日本薬学会の論文
- 2000-10-01
著者
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HASHIMOTO Yuichi
Institute of Molecular & Cellular Biosciences, The University of Tokyo
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Hashimoto Yuichi
Univ. Tokyo Tokyo Jpn
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Hashimoto Yuichi
Institute Of Molecular And Cellular Biosciences University Of Tokyo
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SODEOKA Mikiko
Institute of Molecular and Cellular Biosciences, University of Tokyo
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SOU Sonei
Institute of Molecular and Cellular Biosciences, University of Tokyo
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TAKAHASHI Hiroyasu
Institute of Molecular and Cellular Biosciences, University of Tokyo
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YAMASAKI Ryu
Institute of Molecular and Cellular Biosciences, University of Tokyo
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Hashimoto Y
Graduate School Of Pharmaceutical Sciences Kyushu University
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Hashimoto Yuichi
Institute Of Molecular & Cellular Biosciences University Of Tokyo
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山崎 亮治
徳大医公衛
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Takahashi H
Institute Of Pharmacognosy Faculty Of Pharmaceutical Sciences Tokushima Bunri University
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Sou Sonei
Institute Of Molecular And Cellular Biosciences University Of Tokyo
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Yamasaki R
Graduate School Of Pharmaceutical Sciences University Of Tokyo
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Sodeoka Mikiko
Sagami Chemical Research Center
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Takahashi Hiroyasu
Institute Of Molecular And Cellular Biosciences University Of Tokyo
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Takahashi Hiroyasu
Institute of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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Sodeoka Mikiko
Institute for Chemical Reaction Science, Tohoku University
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