Biological implications of the reaction possibilities of the proximate carcinogenic compound,N-hydroxy-2-fluorenylacetamide
Author:
Publisher
Wiley
Subject
Molecular Medicine,Biochemistry,Spectroscopy
Reference10 articles.
1. The Metabolic Activation of Carcinogenic Aromatic Amines and Amides1
2. Sulfotransferase Activation of N-Hydroxy-2-acetylaminofluorene in Rodent Livers Susceptible and Resistant to this Carcinogen
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2. Formation of N-hydroxy-N-arylacetamides from nitroso aromatic compounds by the mammalian pyruvate dehydrogenase complex;Biochemical Journal;1993-03-15
3. N6-Adenyl arylation of DNA by aristolochic acid II and a synthetic model for the putative proximate carcinogen;Chemical Research in Toxicology;1991-09
4. Gas chromatography-mass spectrometry analysis of tert.-butyldimethylsilyl derivatives of 2-acetylaminofluorene and metabolites in isolated rat hepatocytes;Cell Biology and Toxicology;1987-09
5. High resolution mass spectrometric and high-field nuclear magnetic resonance spectroscopic studies of the herbicide propanil, itsN-oxidative decomposition products and related compounds;Biological Mass Spectrometry;1986-09
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