Abstract
The naphthoquinone lapachol (1) is readily metabolized by several fungi and streptomycetes. Preparative-scale fermentations with Penicillium notatum (UI 1602) provided a major polar metabolite (4), which was isolated and identified as an intermediate of the Hooker oxidation. The metabolite was synthesized by reacting lapachol with hydrogen peroxide under alkaline conditions.
Cite
CITATION STYLE
APA
Otten, S., & Rosazza, J. P. (1978). Microbial transformations of natural antitumor agents: oxidation of lapachol by Penicillium notatum. Applied and Environmental Microbiology, 35(3), 554–557. https://doi.org/10.1128/aem.35.3.554-557.1978
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