Stereoselective Reactions. XVIII. : Synthesis and Cytotoxicity of the Demethyl Derivatives of Steganes
スポンサーリンク
概要
- 論文の詳細を見る
Demethyl derivatives of steganes and deoxypodorhizon, 3,4,6,7,9,10,12,13,18,23,were prepared by the selective demethylation of the methoxy group of steganes and deoxypodorhizon, 2,5,8,11,22. The cytotoxicity of these derivatives was evaluated against KB cell and was found not to exceed that of the parent steganes. 4-Demethyldexypodorhizon (18) was found to show more potent cytotoxicity than deoxypodorhizon (22).
- 公益社団法人日本薬学会の論文
- 1990-07-25
著者
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古賀 憲司
Faculty of Pharmaceutical Sciences, University of Tokyo
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古賀 憲司
東京大学
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Koga Kenjiro
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Hokuriku University
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富岡 清
Faculty of Pharmaceutical Sciences, University of Tokyo
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河崎 久
Faculty of Pharmaceutical Sciences, University of Tokyo
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