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Main Title Inhibitation of Benzo(A)Pyrene Monooxygenase by alpha-Naphthoflavone may be Partially Mediated by the Metabolite 9-Hydroxy-alpha-Naphthoflavone.
Author Nesnow, Stephen ; Easterling, Robert ; Bergman, Hinda ; Roth, Robert ;
CORP Author Health Effects Research Lab., Research Triangle Park, NC.
Year Published 1982
Report Number EPA-600/J-82-153;
Stock Number PB83-189654
Additional Subjects Inhibitors ; Rats ; Liver ; Microsomes ; Metabolism ; Reprints ; Metabolites ; Benzopyrene monooxygenase ; Naphthoflavone ; Naphthoflavone/hydroxy
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NTIS  PB83-189654 Some EPA libraries have a fiche copy filed under the call number shown. 07/26/2022
Collation 10p
Abstract Naphthoflavone (ANF) inhibits beta-naphthoflavon-induced rat liver microsomal benzo(a)pyrene metabolism and is transformed by these microsomes into naphthoflavone metabolites. The authors determined the inhibitory effect on benzo(a)pyrene (B(a)P) metabolism of several of these metabolites and of 6-methoxy-ANF, using beta-naphthoflavone-induced rat liver microsomes. 9-Hydroxy-ANF was the most active inhibitor (I50 = 1.47 micro M) and was metabolized from ANF by these hepatic cimrosomes in concentrations which are inhibitory. Therefore, 9-hydroxy-ANF a microsomal metabolite of ANF, may play a role in the inhibition of B(a)P oxidation by ANF.
Supplementary Notes Pub. in Toxicology Letters, v14 p7-13 1982.
NTIS Title Notes Journal article.
Title Annotations Reprint: Inhibitation of Benzo(A)Pyrene Monooxygenase by alpha-Naphthoflavone may be Partially Mediated by the Metabolite 9-Hydroxy-alpha-Naphthoflavone.
PUB Date Free Form 1982
Category Codes 6T; 6A; 57Y; 57B
NTIS Prices PC A02/MF A01
Primary Description 600/11
Document Type NT
Cataloging Source NTIS/MT
Control Number 320323477
Origin NTIS
Type CAT