Glutathione monoesters.
M E Anderson, A Meister
Index: Anal. Biochem. 183 , 16, (1989)
Full Text: HTML
Abstract
Glutathione monoesters in which the glycine carboxyl group is esterified are effective cellular glutathione delivery agents because they are readily transported into cells and are deesterified intracellularly. In contrast, glutathione itself is not effectively transported into cells. Detailed procedures are given for the preparation of such esters from glutathione and the corresponding alcohol using hydrogen chloride or sulfuric acid as the catalyst.
Related Compounds
Related Articles:
PRIMA-1Met induces myeloma cell death independent of p53 by impairing the GSH/ROS balance.
2014-09-04
[Blood 124(10) , 1626-36, (2014)]
Dual-targeting of aberrant glucose metabolism in glioblastoma.
2015-01-01
[J. Exp. Clin. Cancer Res 34 , 14, (2015)]
Fibroblasts that resist cigarette smoke-induced senescence acquire profibrotic phenotypes.
2014-09-01
[Am. J. Physiol. Lung Cell. Mol. Physiol. 307(5) , L364-73, (2014)]
2001-09-15
[Biochem. Pharmacol. 62 , 787-794, (2001)]
Glutathione monoethyl ester: preparation, uptake by tissues, and conversion to glutathione.
1985-06-01
[Arch. Biochem. Biophys. 239 , 538, (1985)]