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Quantitation of the tetrachloroethylene metaboliteN-acetyl-S-(trichlorovinyl)cysteine in rat urinevia negative ion chemical ionization gas chromatography/tandem mass spectrometry

Data up to Jan 2025

Published1994
Citations17
References18

Total Citations Per Year

Abstract

References (18)

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Identification of S-1,2-dichlorovinyl-N-acetyl-cysteine as a urinary metabolite of trichloroethylene: A possible explanation for its nephrocarcinogenicity in male rats

1986 • 116 citations

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Identification of S‐1,2,2‐trichlorovinyl‐N‐acetylcysteine as a urinary metabolite of tetrachloroethylene: Bioactivation through glutathione conjugation as a possible explanation of its nephrocarcinogenicity

1986 • 91 citations

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1986 • 27 citations

Quantitative determination ofN-acetyl(-L-)cysteine derivatives in human urine by tandem mass spectrometry

1993 • 20 citations

Identification and quantitative determination of four different mercapturic acids formed from 1,3-dibromopropane and its 1,1,3,3-tetradeutero analogue by the rat

1986 • 19 citations

Isotopic exchange during derivatization of platelet activating factor for gas chromatography-mass spectrometry

1991 • 14 citations

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1993 • 14 citations

Gas chromatographic/tandem mass spectrometric identification and quantitation of metabolic 4-acetyltoluene-2,4-diamine from the F344 rat

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Quantitation of the tetrachloroethylene metaboliteN-acetyl-S-(trichlorovinyl)cysteine in… (1994) – Biological Mass Spectrometry | Metascience Observatory Explorer