| Literature DB >> 1159695 |
J P Rosazza, A W Stocklinski, M A Gustafson, J Adrian, R V Smith.
Abstract
Microbial transformations of 10,11-dimethoxyaporphine were studied to determine the potential of microorganisms to produce monomethoxyaporphines. Ten microorganisms were identified as being capable of yielding apocodeine and/or isoapocodeine as the major metabolite in 24 and 20% yield, respectively. Cunninghamella blakesleeana (ATCC 9245) converted 10,11-dimethoxyaporphine quantitatively into isapocodeine. O-Dealkylation of this aporphine system is a facile microbial transformation, and the 10-methoxyl group is more susceptible to metabolic cleavage than the sterically hindered 11-methoxyl group. Selectivity in O-dealkylation may be accomplished with different microorganisms. This is the first report dealing with the microbial transformation of an aporphine system.Entities:
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Year: 1975 PMID: 1159695 DOI: 10.1021/jm00242a006
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446