In vitro inhibition of mouse and rat glutathione S-transferases by di(2-ethylhexyl) phthalate, mono(2-ethylhexyl) phthalate, 2-ethylhexanol, 2-ethylhexanoic acid and clofibric acid.

@article{Law1991InVI,
  title={In vitro inhibition of mouse and rat glutathione S-transferases by di(2-ethylhexyl) phthalate, mono(2-ethylhexyl) phthalate, 2-ethylhexanol, 2-ethylhexanoic acid and clofibric acid.},
  author={M Y Law and David E. Moody},
  journal={Toxicology in vitro : an international journal published in association with BIBRA},
  year={1991},
  volume={5 3},
  pages={207-10}
}
The in vitro inhibitory response of mouse and rat liver cytosolic glutathione S-transferase (GST) activities using the substrates 1,2-dichloro-4-nitrobenzene (DCNB) and 1,2-epoxy-3-(p-nitrophenoxy)propane (ENPP) was determined for the peroxisome proliferators di(2-ethylhexyl) phthalate (DEHP), mono(2-ethylhexyl) phthalate (MEHP), 2-ethylhexanol, 2-ethylhexanoic acid and clofibric acid. MEHP was a potent inhibitor of GST activities in both species, with IC(50)s for DCNB and ENPP of 0.34 and 0.10… CONTINUE READING

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