K4 Elite
Longevity & Cellular
L-Glutathione (GSH) is a very small protein-like molecule (called a tripeptide, meaning it is made of three linked building blocks: glutamate, cysteine and glycine). It is the most common of its kind inside the cells of humans and animals. One part of it (a sulfur-containing group) is very reactive, which makes it important in the cell's chemistry. In the lab it is used as a standard antioxidant (a molecule that protects cells from a type of chemical damage) and as a helper molecule for certain enzymes.
Glutathione switches back and forth between two forms: a "loaded" form (GSH) and a "used-up" paired form (GSSG). Published biochemistry describes it as a molecule that soaks up harmful, unstable particles (free radicals) and other reactive chemicals. It also acts as a required helper for several enzymes, and the balance between its two forms is used as a key sign of how much chemical stress a cell is under [1][2].
Test-tube and animal studies have looked at how glutathione neutralizes damaging chemicals such as hydrogen peroxide and certain fat-related compounds. It can also attach reversibly to proteins (a change called S-glutathionylation), which researchers have studied as a way cells send internal signals [2][3]. Tissue studies have examined how diet and chemical stress change how much glutathione is present [3].
Researchers have studied glutathione as the molecule that attaches to and helps remove harmful foreign chemicals and reactive by-products, with the help of a family of enzymes (glutathione S-transferases). It has also been studied in the handling of certain reactive sugar-related compounds [1][2].
Glutathione, and treatments that either lower or restore it, have been used as tools in cell-culture and rodent studies of chemical stress. Lab methods for measuring the two forms of glutathione have been reviewed as a way to measure results in this kind of work [1][2].
The referenced work is mostly basic chemistry, done in test tubes or animals, or reviews that report mixed results. It does not show that L-Glutathione as supplied here is safe, effective, or beneficial for any health purpose in people. This material is offered strictly for in-vitro research use only (test-tube and lab research only).
| Molecular formula | C10H17N3O6S |
|---|---|
| Molecular weight | 307.32 g/mol |
| PubChem | CID 124886 ↗ |
For laboratory use, lyophilized L-glutathione is typically stored at -20°C and protected from light and moisture; the free thiol is oxygen-sensitive. Reconstitute with sterile or bacteriostatic water (or an appropriate buffer) to prepare working stocks, keep reconstituted solutions refrigerated at 2-8°C, prepare fresh where possible, and minimize freeze-thaw cycles to limit oxidation to the disulfide (GSSG) form.