Issue 11, 1977

Oxidative bonding of natural oestrogens to DNA by chemical and metabolic means

Abstract

Oestradiol and oestrone can be covalently bonded to DNA as a result of oxidation by iodine or hydrogen peroxide and, alternatively, by incubation with a rat liver microsomal preparation in vitro: radioisotope studies show that these processes are mechanistically distinct.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 386-387

Oxidative bonding of natural oestrogens to DNA by chemical and metabolic means

G. M. Blackburn, L. Orgee and G. M. Williams, J. Chem. Soc., Chem. Commun., 1977, 386 DOI: 10.1039/C39770000386

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