(Q66920810)

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Deoxyribonucleic acid binding of 3-hydroxy- and 9-hydroxybenzo[a]pyrene following further metabolism by mouse liver microsomal cytochrome P1-450

scientific article published on May 15, 1979

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31 August 2019

Deoxyribonucleic acid binding of 3-hydroxy- and 9-hydroxybenzo[a]pyrene following further metabolism by mouse liver microsomal cytochrome P1-450 (English)

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31 August 2019

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10.1016/0006-2952(79)90175-8

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Ida Stephens Owens

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I S Owens

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31 August 2019

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C. Legraverend

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1 June 2023

O. Pelkonen

3

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1 May 1979

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31 August 2019

15 May 1979

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National Center for Biotechnology Information

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1 June 2023

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https://api.elsevier.com/content/article/PII:0006295279901758?httpAccept=text/plain

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10.1016/0006-2952(79)90175-8

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Biochemical Pharmacology

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31 August 2019

28

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31 August 2019

10

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31 August 2019

1623-1629

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31 August 2019

Enzymatic conjugation of benzo (a) pyrene oxides, phenols and dihydrodiols with UDP-glucuronic acid

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Benzo(a)pyren-3-yl hydrogen sulphate, a major ethyl acetate-extractable metabolite of benzo(a)pyrene in human, hamster and rat lung cultures

2

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Metabolism of monohydroxybenzo(a)pyrenes by rat liver microsomes and mammalian cells in culture

3

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Kinetic studies of benzpyrene and hydroxybenzpyrene metabolism

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The role of 9-hydroxybenzo(a)pyrene in the microsome mediated binding of benzo(a)pyrene to DNA

6

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Mutagenesis of certain benzo[a]pyrene phenols in vitro following further metabolism by mouse liver

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Cancer Research

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author name string

Cohen

publication date

1977

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Cancer Research

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Baird

publication date

1973

1 reference

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Effects of microsomal enzyme inducers in vivo and inhibitors in vitro on the covalent binding of benzo[a]pyrene metabolites to DNA catalyzed by liver microsomes from genetically responsive and nonresponsive mice

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Exceptional mutagenicity of a benzo[a]pyrene diol epoxide in cultured mammalian cells

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High mutagenicity and toxicity of a diol epoxide derived from benzo(a)pyrene

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Metabolic activation of benzo(a)pyrene proceeds by a diol-epoxide

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Metabolism of benzo[a]pyrene. Effect of substrate concentration and 3-methylcholanthrene pretreatment on hepatic metabolism by microsomes from rats and mice

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Microsomal metabolism on benzo(a)pyrene. Multiple effects of epoxide hydrase inhibitors

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Conversion of naphthalene to trans-naphthalene dihydrodiol: Evidence for the presence of a coupled aryl monooxygenase-epoxide hydrase system in hepatic microsomes

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10.1016/0006-2952(79)90175-8

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:475823%20AND%20SRC:MED&resulttype=core&format=json

31 August 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:475823%20AND%20SRC:MED&resulttype=core&format=json

31 August 2019

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