BIOSYNTHESIS OF CHALCOMORACIN AND KUWANON J, THE DIELS-ALDER TYPE ADDUCTS, IN MORUS ALBA L. CELL CULTURES
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概要
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Experiments with [1-^<13>C]-, [2-^<13>C]- and [1,2-^<13>C_2]-acetates administered to Morus alba cell cultures revealed that both optically active Diels-Alder type adducts chalcomoracin (1) and kuwanon J (2) are formed through the condensation of two molecules of cinnamoylpolyketide-derived skeletons. The 2-arylbenzofuran skeleton of 1 is formed by a novel type cyclization of the cinnamoylpolyketide, followed by decarboxylation. The ^<13>C-labeling of [2-^<13>C] acetate was incorporated into the starter acetate carbons in the biosynthesis of the prenyl moieties of chalcomoracin (1), while that of [1-^<13>C] acetate was not incorporated into the prenyl moieties of 1.
- 社団法人日本薬学会の論文
- 1989-02-25
著者
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上田 伸一
Faculty Of Pharmaceutical Sciences Kyoto University
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上田 伸一
京大・薬
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羽野 芳生
Faculty of Pharmaceutical Sciences, Toho University
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野村 太郎
Faculty of Pharmaceutical Sciences, Toho University
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野村 太郎
Faculty Of Pharmaceutical Sciences Toho University
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野村 太郎
東邦大 薬
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羽野 芳生
東邦大薬
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