LC-APCI(−)-MS Determination of 1-Chloro-2,4-dinitrobenzene, a Model Substrate for Glutathione S-Transferases-Reference-Cited by-同舟云学术

LC-APCI(−)-MS Determination of 1-Chloro-2,4-dinitrobenzene, a Model Substrate for Glutathione S-Transferases

Published:2020-01-24 Issue:3 Volume:31 Page:467-472
ISSN:1044-0305
Container-title:Journal of the American Society for Mass Spectrometry
language:en
Short-container-title:J. Am. Soc. Mass Spectrom.

Author:

Tierbach Alena¹²,Groh Ksenia J³,Schönenberger René¹,Schirmer Kristin¹²⁴^ORCID,Suter Marc J-F¹⁴^ORCID

Affiliation:

1. Eawag, Swiss Federal Institute of Aquatic Science and Technology, 8600 Dübendorf, Switzerland

2. EPF Lausanne, School of Architecture, Civil and Environmental Engineering, 1015 Lausanne, Switzerland

3. Food Packaging Forum Foundation, 8045 Zürich, Switzerland

4. ETH Zürich, Department of Environmental Systems Science, 8092 Zürich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Spectroscopy,Structural Biology

Link

https://pubs.acs.org/doi/pdf/10.1021/jasms.9b00116

Reference10 articles.

1. HSDB, Hazardous Substances Data Bank [Internet]; National Library of Medicine (US), Bethesda (MD); (5/17/2012; cited 2019 Jun). 1-CHLORO-2,4-DINITROBENZENE; Hazardous Substances Databank Number: 5306. Available from: http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?HSDB.

2. Intrinsic Xenobiotic Metabolizing Enzyme Activities in Early Life Stages of Zebrafish (Danio rerio)

3. Intrahepatic conversion of a glutathione conjugate to its mercapturic acid. Metabolism of 1-chloro-2,4-dinitrobenzene in isolated perfused rat and guinea pig livers.

4. Glutathione S-Transferases

5. Simultaneous determination of 1-chloro-2,4-dinitrobenzene, 2,4-dinitrophenyl-S-glutathione and its metabolites for human placental disposition studies by high-performance liquid chromatography

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