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AbstractAbstract
[en] Oral administration of 1,3-dibromopropane (2 mmol/kg) to rats resulted in a marked decrease in the level of hepatic glutathione (GSH). Sulphur-containing [14C]metabolites were excreted in the bile of rats dosed with 1,3-bromo[14C]propane and were subjected to enterohepatic cycling. After an oral dose of 1,3-dibromo[14C]propane, peak levels of radioactivity were rapidly attained in the blood and were maintanied for several hours; approximately equal amounts of radioactive material were excreted in urine and expired air. Several radioactive metabolites were excreted in urine; a major metabolite was N-acetyl-S-[1-bromo-3-propyl]-cysteine. (Auth.)
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Record Type
Journal Article
Journal
Toxicology Letters; ISSN 0378-4274;
; v. 8(1-2); p. 7-15

Country of publication
ALKANES, ANIMALS, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, BIOLOGICAL MATERIALS, BIOLOGICAL WASTES, BODY FLUIDS, CARBON ISOTOPES, CLEARANCE, EVEN-EVEN NUCLEI, EXCRETION, HYDROCARBONS, ISOTOPES, KINETICS, LIGHT NUCLEI, MAMMALS, NUCLEI, ORGANIC COMPOUNDS, PEPTIDES, POLYPEPTIDES, PROTEINS, RADIOISOTOPES, RODENTS, VERTEBRATES, WASTES, YEARS LIVING RADIOISOTOPES
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