Science · 1970 · 33 citations · 12 references
BiosynthesisMolecular PhysiologyBiochemistryEndocrine MechanismMedicineOncogenic AgentPhysiologySecondary MetaboliteChemical Oncogen 3-HydroxyxanthineOncogenic Purine DerivativesEndocrinologyProximate OncogenReactive IntermediateMetabolomicsMetabolismPharmacologyExperimental ToxicologyPrimary Metabolite
Two additional urinary metabolites of the chemical oncogen 3-hydroxyxanthine are now identified as 8-chloroxanthine and 8-methylmercaptoxanthine. Such products are thought to be derived from a reactive intermediate which can be tentatively considered to be a proximate oncogen. Since each of these 8-substituted xanthines has also been obtained in vitro by reactions of 3-acetoxyxanthine with chloride ion or methionine, their production in vivo can be explained as resulting through the metabolic formation of an activated ester with a reactivity similar to that of the chemical model.
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Jack R. DeBaun, James Rowley, Elizabeth C. Miller et al. · Experimental Biology and Medicine · 1968 · 114 citations
Aldo-keto Reductase, Rodent Livers Susceptible, Pathology +18
Gerhard Stöhrer, George Bosworth Brown · Journal of Biological Chemistry · 1969 · 45 citations · Full text