Nephrotoxic and genotoxic N-acetyl-S-dichlorovinyl-L-cysteine is a urinary metabolite after occupational 1,1,2-trichloroethene exposure in humans: implications for the risk of trichloroethene exposure (Q35031501)

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Language	Label	Description	Also known as
English	Nephrotoxic and genotoxic N-acetyl-S-dichlorovinyl-L-cysteine is a urinary metabolite after occupational 1,1,2-trichloroethene exposure in humans: implications for the risk of trichloroethene exposure	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Nephrotoxic and genotoxic N-acetyl-S-dichlorovinyl-L-cysteine is a urinary metabolite after occupational 1,1,2-trichloroethene exposure in humans: implications for the risk of trichloroethene exposure (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

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author name string

Birner G

1

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Europe PubMed Central

PubMed publication ID

5 August 2017

Vamvakas S

2

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Europe PubMed Central

PubMed publication ID

5 August 2017

Dekant W

3

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Europe PubMed Central

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5 August 2017

Henschler D

4

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Europe PubMed Central

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5 August 2017

publication date

1 March 1993

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Europe PubMed Central

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5 August 2017

Environmental Health Perspectives

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5 August 2017

99

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Europe PubMed Central

PubMed publication ID

5 August 2017

281-284

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Europe PubMed Central

PubMed publication ID

5 August 2017

Biochemical, histological, and ultrastructural changes in rat and mouse liver following the administration of trichloroethylene: possible relevance to species differences in hepatocarcinogenicity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1567030

8 July 2018

Metabolic conversion of tri- and tetrachloroethylene: formation and deactivation of genotoxic intermediates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1567030

8 July 2018

Bacterial beta-lyase mediated cleavage and mutagenicity of cysteine conjugates derived from the nephrocarcinogenic alkenes trichloroethylene, tetrachloroethylene and hexachlorobutadiene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1567030

8 July 2018

Metabolism of trichloroethene--in vivo and in vitro evidence for activation by glutathione conjugation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1567030

8 July 2018

Bioactivation of xenobiotics by formation of toxic glutathione conjugates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1567030

8 July 2018

Identification of N-acetyl(2,2-dichlorovinyl)- and N-acetyl(1,2-dichlorovinyl)-L-cysteine as two regioisomeric mercapturic acids of trichloroethylene in the rat.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1567030

8 July 2018

Identifiers

10.1289/EHP.9399281

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

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