Abstract
Two mercapturic acids, i. e., N-acetyl-S-(1-cyano-2-hydroxyethyl)-l-cysteine (CHEMA) and N-acetyl-S(2-hydroxyethyl)-l-cysteine (HEMA), were isolated from the urine of rats dosed with four successive doses of oxiranecarbonitrile (glycidonitrile, GN), 5 mg/kg, a reactive metabolic intermediate of acrylonitrile (AN). GC-MS analysis of methylated urine extracts from both AN- and GN-dosed rats showed another mercapturate which was identified as N-acetyl-S-(1-cyanoethenyl)-l-cysteine (1-CEMA) methyl ester using an authentic reference sample. The mass spectrum of this compound was very similar to that of a methylated metabolite of AN tentatively identified by Langvardt et al. (1980) as N-acetyl-3-carboxy-5-cyanothiazane (ACCT). In contrast, no ACCT was found in rats dosed with either GN or AN. Hence, there is no evidence for the formation of ACCT or its isomers in rats dosed with AN or GN. The methyl ester of 1-CEMA is formed artificially by dehydration of CHEMA methyl ester in the injector of the gas chromatograph.
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Details of the synthetic procedures and NMR-spectra are available from the authors on request
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Linhart, I., Šmejkal, J. & Novák, J. N-ccetyl-S-(1-cyano-2-hydroxyethyl)-l-cysteine, a new urinary metabolite of acrylonitrile and oxiranecarbonitrile. Arch Toxicol 61, 484–488 (1988). https://doi.org/10.1007/BF00293695
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DOI: https://doi.org/10.1007/BF00293695