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Metabolism and distribution of 3,4-epithiobutanenitrile in the rat
Authors:E.R. Brocker  M.H. Benn  J. Lüthy  A. von Däniken
Affiliation:Department of Chemistry, The University, Calgary, Alberta, Canada T2N 1N4;Institut für Toxikologie der ETH und der Universität Zürich, Schorenstrasse 16, CH-8603 Schwerzenbach, Switzerland
Abstract:The metabolism and distribution of [2-14C]- and 35S-labelled 3,4-epithiobutanenitrile (4ETN), a thiirane occurring naturally in cruciferous vegetables, was studied in the rat. A dose of c. 11 mg 4ETN/kg body weight was rapidly transformed into water-soluble compounds and was mainly excreted in the urine, irrespective of the route of administration (oral or ip). The main metabolite in the urine was identified by gas chromatography-mass spectrometry as a mercapturic acid derivative. Low residual radioactivity demonstrated in organs 72 hr after administration was consistent with an earlier report that the thiirane may function as a weak biological alkylating agent.
Keywords:4ETN  3,4-Epithiobutanenitrile  GC  gas chromatography  MS  mass spectrometry  NMR  nuclear magnetic resonance  TLC  thin-layer chromatography
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