Compounds > s-(1,2-dichlorovinyl)cysteine
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s-(1,2-dichlorovinyl)cysteine and Sensitivity and Specificity

s-(1,2-dichlorovinyl)cysteine has been researched along with Sensitivity and Specificity in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dekant, W; Völkel, W1
Abraham, DG; Cooper, AJ1

Other Studies

2 other study(ies) available for s-(1,2-dichlorovinyl)cysteine and Sensitivity and Specificity

ArticleYear
Chlorothioketene, the ultimate reactive intermediate formed by cysteine conjugate beta-lyase-mediated cleavage of the trichloroethene metabolite S-(1,2-Dichlorovinyl)-L-cysteine, forms cytosine adducts in organic solvents, but not in aqueous solution.
    Chemical research in toxicology, 1998, Volume: 11, Issue:9

    Topics: Acetates; Animals; Carbon-Sulfur Lyases; Cattle; Cysteine; Cytosine; DNA; DNA Adducts; Gas Chromatography-Mass Spectrometry; Ketones; Sensitivity and Specificity; Solutions; Solvents; Water

1998
Glutamine transaminase K and cysteine S-conjugate beta-lyase activity stains.
    Analytical biochemistry, 1991, Sep-02, Volume: 197, Issue:2

    Topics: Animals; Cysteine; Electrophoresis, Polyacrylamide Gel; Kidney; Lyases; Methionine; Molecular Weight; Nitroblue Tetrazolium; Phenylalanine; Rats; Rats, Inbred Strains; Sensitivity and Specificity; Staining and Labeling; Transaminases

1991