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Biosynthesis of diterpenoid aphidicolin: Isolation of intermediates from P-450 inhibitor treated mycelia of Phoma betae

H Oikawa, S Ohashi, A Ichihara, S Sakamura

文献索引:Oikawa, Hideaki; Ohashi, Satoshi; Ichihara, Akitami; Sakamura, Sadao Tetrahedron, 1999 , vol. 55, # 24 p. 7541 - 7554

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被引用次数: 19

摘要

Treatment of Phoma betae with P-450 inhibitors caused accumulation of biosynthetic precursors 2, 3 and 4 of aphidicolin (1). Their structures were elucidated by spectroscopic analysis and they were confirmed by chemical transformations from 1. Isotopically labeled precursors were synthesized by either reductive deoxygenation of aphidicolin derivatives or microbial conversion of [1-14C] acetate in the presence of the P-450 inhibitor. Feeding ...