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Glutathione-diethyl ester (reduced) (CAS 97451-40-6)

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Alternate Names:
H-Glu(Cys-Gly-OEt)-OEt; GSH diethyl ester
Application:
Glutathione-diethyl ester (reduced) is a glutathione analog
CAS Number:
97451-40-6
Molecular Weight:
363.43
Molecular Formula:
C14H25N3O6S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Glutathione-diethyl ester (reduced) is a derivative of the naturally occurring tripeptide glutathione, which is pivotal in cellular antioxidant defense mechanisms. This specific ester form enhances the bioavailability of glutathione when introduced into biological systems, allowing for more effective penetration into cells compared to the native form. The chemical serves as a critical tool in oxidative stress research by facilitating the increase of intracellular glutathione levels. This increment is essential for studying various oxidative processes and the cellular responses to reactive oxygen species (ROS). Researchers utilize this compound to investigate how enhanced glutathione levels can influence redox-sensitive signaling pathways, gene expression, and overall cellular health. Moreover, Glutathione-diethyl ester is employed in experimental settings to assess the impact of glutathione on cellular detoxification processes, including the neutralization of harmful byproducts of metabolism and xenobiotic detoxification. Its use is crucial in the fields of molecular biology and biochemistry, particularly in studies related to aging, neurodegeneration, and the cellular mechanisms underlying stress responses. By modulating glutathione levels, scientists can dissect the protective roles of this peptide in maintaining cellular homeostasis against environmental and metabolic stress.


Glutathione-diethyl ester (reduced) (CAS 97451-40-6) References

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  2. Mechanisms of ammonia-induced cell death in rat cortical neurons: roles of NMDA receptors and glutathione.  |  Klejman, A., et al. 2005. Neurochem Int. 47: 51-7. PMID: 15985217
  3. Molecular mechanism of glutathione-mediated protection from oxidized low-density lipoprotein-induced cell injury in human macrophages: role of glutathione reductase and glutaredoxin.  |  Wang, Y., et al. 2006. Free Radic Biol Med. 41: 775-85. PMID: 16895798
  4. Ammonia increases paracellular permeability of rat brain endothelial cells by a mechanism encompassing oxidative/nitrosative stress and activation of matrix metalloproteinases.  |  Skowrońska, M., et al. 2012. J Neurochem. 121: 125-34. PMID: 22260250
  5. Chronic depletion of glutathione exacerbates ventricular remodelling and dysfunction in the pressure-overloaded heart.  |  Watanabe, Y., et al. 2013. Cardiovasc Res. 97: 282-92. PMID: 23129588
  6. The Glutathione Derivative, GSH Monoethyl Ester, May Effectively Whiten Skin but GSH Does Not.  |  Chung, BY., et al. 2016. Int J Mol Sci. 17: PMID: 27128906
  7. Comparison of the delivery of reduced glutathione into P388D1 cells by reduced glutathione and its mono- and diethyl ester derivatives.  |  Minhas, HS. and Thornalley, PJ. 1995. Biochem Pharmacol. 49: 1475-82. PMID: 7763291
  8. Preparation and properties of glutathione diethyl ester and related derivatives.  |  Levy, EJ., et al. 1994. Methods Enzymol. 234: 499-504. PMID: 7808324
  9. Transport of glutathione diethyl ester into human cells.  |  Levy, EJ., et al. 1993. Proc Natl Acad Sci U S A. 90: 9171-5. PMID: 8415673
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Glutathione-diethyl ester (reduced), 250 mg

sc-295012
250 mg
$714.00

Glutathione-diethyl ester (reduced), 1 g

sc-295012A
1 g
$2129.00