The metabolic activation of dibenzo[a,e]fluoranthene in vitro. Evidence that its bay-region and pseudo-bay-region diol-epoxides react preferentially with guanosine

Author:

Perin-Roussel O.,Croisy A.,Ekert B.,Zajdela F.

Publisher

Elsevier BV

Subject

Cancer Research,Oncology

Reference25 articles.

1. Isolation of the hydrocarbon-deoxyribonucleoside products from the DNA of mouse embryo cells treated in culture with 7-methylbenz(a)anthracene-3H;Baird;Cancer Res.,1973

2. Studies on the formation of hydrocarbon-deoxyribonucleoside products by the binding of derivatives of 7-methyl-benz(a)anthracene to DNA in aqueous solution and in mouse embryo cells in culture;Baird;Cancer Res.,1973

3. Evidence for the binding of polynuclear aromatic hydrocarbons to the nucleic acids to mouse skin: Relation between carcinogenic power of hydrocarbons and their binding to deoxyribonucleic acid;Brookes;Nature,1964

4. Symposium Radiation Chemistry of DNA and DNA Model Compounds;Cadet,1979

5. The metabolic activation of benz[a]-anthracene in hamster embryo cells: evidence that diol-epoxides react with guanosine, deoxyguanosine and adenosine in nucleic acids;Cooper;Chem.-Biol. Interact.,1980

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