Synthesis and Evaluation of Iodinated Benzamide Derivatives as Selective and Reversible Monoamine Oxidase B Inhibitors
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概要
- 論文の詳細を見る
A new series of iodinated analogues of N-(2-aminoethyl)benzamide was synthesized and evaluated for inhibitory potency and specificity toward monoamine oxidase type-B (MAO-B). Among them, N-(2-aminoethyl)-2-chloro-4-iodobenzamide hydrochloride (2d) showed high inhibitory potency and selectivity against MAO-B. The type of MAO-B inhibition by 2d was non-competitive and the inhibition constant (K_i) was 0.80 μM. Strong and selective in vivo MAO-B inhibition by 2d was also confirmed. The brain MAO-B inhibition by 2d was reversible and the enzyme activity completely returned to the control value 24 h after administration. Compound 2d was, therefore, considered to be a candidate for advanced development as a radioiodinated ligand that may be useful for functional MAO-B studies in the living brain using single photon emission computer tomography.
- 社団法人日本薬学会の論文
- 1992-07-25
著者
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横山 陽
Faculty of Pharmaceutical Sciences, Kyoto University
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横山 陽
京都大学薬学部
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間賀田 泰寛
京都大学医学部
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大桃 善朗
Osaka University of Pharmaceutical Sciences
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村上 勝彦
Osaka University of Pharmaceutical Sciences
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平田 雅彦
Faculty of Pharmaceutical Sciences Kyoto University
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田中 千秋
Osaka University of Pharmaceutical Sciences
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杉本 淳
Osaka University of Pharmaceutical Sciences
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間賀田 泰寛
Faculty of Medicine, Kyoto University
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宮原 直子
Osaka University of Pharmaceutical Sciences
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間賀田 泰寛
京都大学医学部放射線核医学講座
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横山 陽
京大
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田中 千秋
Osaka College Of Pharmacy
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