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.

Download full-text PDF

Source
http://dx.doi.org/10.1007/BF00293695DOI Listing

Publication Analysis

Top Keywords

rats dosed
12
methyl ester
12
n-acetyl-s-1-cyano-2-hydroxyethyl-l-cysteine urinary
4
urinary metabolite
4
metabolite acrylonitrile
4
acrylonitrile oxiranecarbonitrile
4
oxiranecarbonitrile mercapturic
4
mercapturic acids
4
acids n-acetyl-s-1-cyano-2-hydroxyethyl-l-cysteine
4
n-acetyl-s-1-cyano-2-hydroxyethyl-l-cysteine chema
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!