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pubmed-article:6746720pubmed:abstractTextThe objective of this study was to compare urinary metabolism of parent 3,3-dimethyl-1-phenyltriazene with that of its ring-substituted 1-(4-chlorophenyl)-3,3-dimethyltriazene and 1-(2,4,6-trichlorophenyl)-3,3-dimethyltriazene congeners, in an attempt to evaluate the molecular requirements for systemic carcinogenic activity. Complementary carcinogenicity assays were conducted at low equimolar dose levels using both 4- und 2,4,6-chlorinated and brominated analogues. Ring halogenation was found to prolong metabolic detoxification and to reduce carcinogenic activity.lld:pubmed
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pubmed-article:6746720pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:6746720pubmed:year1984lld:pubmed
pubmed-article:6746720pubmed:articleTitleComparative metabolism and carcinogenicity of ring-halogenated 3,3-dimethyl-1-phenyltriazenes.lld:pubmed
pubmed-article:6746720pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:6746720pubmed:publicationTypeComparative Studylld:pubmed