Microbial models of mammalian metabolism. O-Dealkylation of 10,11-dimethoxyaporphine

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....

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Veröffentlicht in:Journal of medicinal chemistry 1975-08, Vol.18 (8), p.791-794
Hauptverfasser: Rosazza, J. P, Stocklinski, A. W, Gustafson, M. A, Adrian, J, Smith, R. V
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Sprache:eng
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Zusammenfassung: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.
ISSN:0022-2623
1520-4804
DOI:10.1021/jm00242a006