Protein Information

Name glutathione S transferases
Synonyms GST class alpha 2; Gst2; GST class alpha; GST class alpha member 2; GST gamma; GSTA 2; GSTA2; GSTA2 2…

Compound Information

Name 2,4,5-T
CAS 2-(2,4,5-trichlorophenoxy)acetic acid

Reference List

PubMed Abstract RScore(About this table)
6719464 Vessey DA, Boyer TD: Differential activation and inhibition of different forms of rat liver glutathione S-transferase by the herbicides 2,4-dichlorophenoxyacetate (2,4-D) and 2,4,5-trichlorophenoxyacetate (2,4,5-T). Toxicol Appl Pharmacol. 1984 May;73(3):492-9.

Glutathione S-transferase form YaYa was maximally inhibited by 72 and 30%, respectively, by 2,4-D and 2,4,5-T.
194(2,3,3,4) Details
4060158 Singh SV, Awasthi YC: Inhibition of human glutathione S-transferases by 2,4-dichlorophenoxyacetate (2,4-D) and 2,4,5-trichlorophenoxyacetate (2,4,5-T). Toxicol Appl Pharmacol. 1985 Nov;81(2):328-36.
31(0,1,1,1) Details
3358263 Vessey DA, Boyer TD: Characterization of the activation of rat liver glutathione S-transferases by nonsubstrate ligands. Toxicol Appl Pharmacol. 1988 Apr;93(2):275-80.

Pharmacol., 35, 289-295) the activity of glutathione S-transferase form YcYc from rat liver was found to be stimulated by the herbicide 2,4,5-T.
7(0,0,1,2) Details
16426233 Vollrath V, Wielandt AM, Iruretagoyena M, Chianale J: Role of Nrf2 in the regulation of the Mrp2 (ABCC2) gene. Biochem J. 2006 May 1;395(3):599-609.

The Nrf2 (nuclear factor-erythroid 2 p45-related factor 2) transcription factor regulates gene expression of the GCLC (glutamate-cysteine ligase catalytic subunit), which is a key enzyme in glutathione synthesis, and GSTs (glutathione S-transferases) via the ARE (antioxidant-response element).
A similar pattern of co-induction of Mrp2 and GCLC genes was also observed in mouse (Hepa 1-6) and human (HepG2) hepatoma cells treated with BHA, beta-NF (beta-naphthoflavone), 2,4,5-T (trichlorophenoxyacetic acid) or 2AAF (2-acetylaminofluorene), suggesting that these genes share common mechanism (s) of transcriptional activation in response to exposure to xenobiotics.
1(0,0,0,1) Details
1494887 James SI, Ahokas JT: Effect of peroxisome proliferators on glutathione-dependent sulphobromophthalein excretion. Xenobiotica. 1992 Dec;22(12):1425-32.

The effect of pretreatment of rats with the peroxisome proliferator 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) on sulphobromophthalein excretion from the isolated perfused rat liver has been investigated and compared with the effect of clofibrate which is also a peroxisome proliferator. 2.
The results of the present study confirm previous studies that have shown an association between peroxisome proliferation treatment and inhibition of glutathione S-transferase-mediated sulphobromophthalein excretion.
1(0,0,0,1) Details
7538273 Daubaras DL, Hershberger CD, Kitano K, Chakrabarty AM: Sequence analysis of a gene cluster involved in metabolism of 2,4,5-trichlorophenoxyacetic acid by Burkholderia cepacia AC1100. Appl Environ Microbiol. 1995 Apr;61(4):1279-89.


Burkholderia cepacia AC1100 utilizes 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) as a sole source of carbon and energy.
0(0,0,0,0) Details