Chem. Pharm. Bull., 53(8),1011-1013, August 2005
The microbial transformation of an oral contraceptive, mestranol (1) by Cunninghamella elegans yielded two hydroxylated metabolites, 6β-hydroxymestranol (2) and 6β,12β-dihydroxymestranol (3). Metabolite 3 was found to be a new compound. These metabolites were structurally characterized on the basis of spectroscopic techniques.
Key words mestranol; 17β-methoxymestranol; microbial transformation; Cunninghamella elegans