Literature DB >> 3448

Identification of dimethylnitrosoamine metabolites in vitro.

S Grilli, G Prodi.   

Abstract

The incubation of dimethylnitrosoamine (DMNA) in the presence of rat liver microsomes leads to production of formaldehyde, formic acid, methylamine, and N-methylhydrazine. When pH 5-enzymes are added to the medium there is also the formation of N-methylhydroxylamide and N,N-dimethylhydrazine. The last compound is the only metabolite produced, to a lesser extent, by the pH 5-enzymes. Thus, the denitrosated or non-denitrosated metabolites are produced either by an oxidative dealkylation and by a reduction of DMNA, catalysed by microsomal and cellular soluble enzymes.

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Year:  1975        PMID: 3448

Source DB:  PubMed          Journal:  Gan        ISSN: 0016-450X


  5 in total

1.  Biodegradation of N-nitrosodimethylamine in aqueous and soil systems.

Authors:  D L Kaplan; A M Kaplan
Journal:  Appl Environ Microbiol       Date:  1985-10       Impact factor: 4.792

2.  Histochemical localization of primary and secondary alcohol dehydrogenases in whole-body, freeze-dried sections of mice.

Authors:  T Egashira; W J Waddell
Journal:  Histochem J       Date:  1984-09

3.  Further studies on dimethylnitrosamine metabolism, activation and its ability to cause liver injury.

Authors:  M I Diaz Gomez; H M Godoy; J A Castro
Journal:  Arch Toxicol       Date:  1981-06       Impact factor: 5.153

4.  Direct alkyl chain cleavage after C-hydroxylation of dialkylnitrosamines in rats. A new pathway of the oxidative biotransformation.

Authors:  L Blattmann
Journal:  Z Krebsforsch Klin Onkol Cancer Res Clin Oncol       Date:  1977

5.  alpha-Hydroxylation pathway in the in vitro metabolism of carcinogenic nitrosamines: N-nitrosodimethylamine and N-nitroso-N-methylaniline.

Authors:  M B Kroeger-Koepke; S R Koepke; G A McClusky; P N Magee; C J Michejda
Journal:  Proc Natl Acad Sci U S A       Date:  1981-10       Impact factor: 11.205

  5 in total

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