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. 1983 Feb;45(2):616–621. doi: 10.1128/aem.45.2.616-621.1983

Microbial Transformations of Natural Antitumor Agents: Products of Rotenone and Dihydrorotenone Transformation by Cunninghamella blakesleeana

F Sima Sariaslani 1, J P Rosazza 1
PMCID: PMC242333  PMID: 16346210

Abstract

Various species of Absidia, Aspergillus, Cunninghamella, Trichothecium, Penicillium, and Phanerochaete were found to transform rotenone to one or more metabolites. Two biotransformation products were isolated from a preparative-scale incubation of rotenone with Cunninghamella blakesleeana and identified as 1′,2′-dihydro-1′,2′-dihydroxyrotenone and 3′-hydroxyrotenone (amorphigenin). The catalytic reduction of the isopropylene side chain of rotenone resulted in the formation of 1′,2′-dihydrorotenone. The latter was transformed by C. blakesleeana to 2′-hydroxy-1′,2′-dihydrorotenone.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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