Abstract:
:The metabolism of the carcinogenic pentacyclic azaaromatic compound, dibenz[a,j]acridine, has been examined in liver microsomal incubations using preparations from 3-methylcholanthrene-pretreated Wistar rats. Using authentic synthetic standards, u.v. spectroscopy and mass spectrometry, the following were proved to be metabolites: trans-5,6-dihydro-5,6-dihydroxydibenz[a,j]acridine, trans-3,4-dihydro-3,4-dihydroxydibenz[a,j]acridine, dibenz[a,j]acridine-5,6-oxide, 3-hydroxydibenz[a,j]acridine and 4-hydroxydibenz[a,j]acridine. The 3,4-dihydrodiol appeared to be the major metabolite. The secondary metabolites were also examined and evidence is presented for the additional formation of dibenz[a,j]acridine-5,6,8,9-dioxide, tetrols, diol epoxides and phenolic dihydrodiols.
journal_name
Carcinogenesisjournal_title
Carcinogenesisauthors
Gill JH,Duke CC,Rosario CA,Ryan AJ,Holder GMdoi
10.1093/carcin/7.8.1371subject
Has Abstractpub_date
1986-08-01 00:00:00pages
1371-8issue
8eissn
0143-3334issn
1460-2180journal_volume
7pub_type
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