Literature DB >> 1159695

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

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.

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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


  3 in total

1.  Demethylation of Veratrole by Cytochrome P-450 in Streptomyces setonii.

Authors:  J B Sutherland
Journal:  Appl Environ Microbiol       Date:  1986-07       Impact factor: 4.792

2.  Novel Biotransformations of 7-Ethoxycoumarin by Streptomyces griseus.

Authors:  F S Sariaslani; J P Rosazza
Journal:  Appl Environ Microbiol       Date:  1983-08       Impact factor: 4.792

3.  Regiospecific synthesis of isoapocodeine from 10,11-dimethoxyaporphine by using Cunninghamella elegans.

Authors:  R V Smith; P J Davis
Journal:  Appl Environ Microbiol       Date:  1978-04       Impact factor: 4.792

  3 in total

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