Glutathione
| Names | |
|---|---|
| IUPAC name
γ-Glutamylcysteinylglycine
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| Systematic IUPAC name
(2S)-2-Amino-5-({(2R)-1-[(carboxymethyl)amino]-1-oxo-3-sulfanylpropan-2-yl}amino)-5-oxopentanoic acid | |
| Other names
γ-L-Glutamyl-L-cysteinylglycine
(2S)-2-Amino-4-({(1R)-1-[(carboxymethyl)carbamoyl]-2-sulfanylethyl}carbamoyl)butanoic acid | |
| Identifiers | |
3D model (JSmol)
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| Abbreviations | GSH |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.000.660 |
| KEGG | |
| MeSH | Glutathione |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C10H17N3O6S | |
| Molar mass | 307.32 g·mol−1 |
| Melting point | 195 °C (383 °F; 468 K) |
| Freely soluble | |
| Solubility in methanol, diethyl ether | Insoluble |
| Pharmacology | |
| V03AB32 (WHO) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Glutathione (GSH, /ˌɡluːtəˈθaɪoʊn/) is a tripeptide made of the amino acids glutamate, cysteine, and glycine. It is an antioxidant in plants, animals, fungi, and some bacteria and archaea. Glutathione is capable of preventing damage to important cellular components caused by sources such as reactive oxygen species, free radicals, peroxides, lipid peroxides, and heavy metals.
It is synthesized by attaching cysteine to the carboxyl group of the glutamate side chain with a gamma peptide linkage, and to glycine with a normal peptide linkage.