Oxidative metabolism of the synthetic estrogens hexestrol and dienestrol indicates reactive intermediates.
暂无分享,去创建一个
[1] M. Metzler. The metabolism of diethylstilbestrol. , 1981, CRC critical reviews in biochemistry.
[2] W. Lutz,et al. In vivo covalent binding of organic chemicals to DNA as a quantitative indicator in the process of chemical carcinogenesis. , 1979, Mutation research.
[3] D. Nebert,et al. Covalent binding of diethylstilbestrol to dna catalyzed by hepatic and uterine microsomes. Abstr. , 1979 .
[4] M. Metzler,et al. Peroxidase-mediated oxidation, a possible pathway for metabolic activation of diethylstilbestrol. , 1978, Biochemical and biophysical research communications.
[5] C. Schlatter,et al. Covalent binding of ethinylestradiol and estrone to rat liver DNA in vivo. , 1978, Chemico-biological interactions.
[6] J. Tsibris,et al. Microsomal activation of estrogens and binding to nucleic acids and proteins. , 1977, Biochemical and biophysical research communications.
[7] G. Blackburn,et al. Oxidative bonding of natural oestrogens to DNA by chemical and metabolic means , 1977 .
[8] G. Blackburn,et al. Binding of diethylstilboestrol to deoxyribonucleic acid by rat liver microsomal fractions in vitro and in mouse foetal cells in culture. , 1976, The Biochemical journal.
[9] M. Metzler. Metabolic activation of carcinogenic diethylstilbestrol in rodents and humans. , 1976, Journal of toxicology and environmental health. Supplement.