Glutathione disulfide
Names | |
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IUPAC name
(2S)-2-amino-5-[[(2R)-3-[(2R)-2-[[(4S)-4-amino-5-hydroxy-5-oxopentanoyl]amino]-3-(carboxymethylamino)-3-oxopropyl]disulfanyl-1- (carboxymethylamino)-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
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Identifiers | |
27025-41-8 | |
Abbreviations | GSSG |
ChEMBL | ChEMBL1372 |
ChemSpider | 58835 |
6835 | |
Jmol 3D model | Interactive image |
PubChem | 65359 11215652 |
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Properties | |
C20H32N6O12S2 | |
Molar mass | 612.631 g/mol |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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verify (what is ?) | |
Infobox references | |
Glutathione disulfide (GSSG) is a disulfide derived from two glutathione molecules.[1]
In living cells, glutathione disulfide is reduced into two molecules of glutathione with reducing equivalents from the coenzyme NADPH. This reaction is catalyzed by the enzyme glutathione reductase.[2] Antioxidant enzymes, such as glutathione peroxidases and peroxiredoxins, generate glutathione disulfide during the reduction of peroxides such as hydrogen peroxide (H2O2) and organic hydroperoxides (ROOH):[3]
- 2 GSH + ROOH → GSSG + ROH + H2O
Other enzymes, such as glutaredoxins, generate glutathione disulfide through thiol-disulfide exchange with protein disulfide bonds or other low molecular mass compounds, such as coenzyme A disulfide or dehydroascorbic acid.[4]
- 2 GSH + R-S-S-R → GSSG + 2 RSH
Neuromodulator
GSSG, along with glutathione and S-nitrosoglutathione (GSNO), have been found to bind to the glutamate recognition site of the NMDA and AMPA receptors (via their γ-glutamyl moieties), and may be endogenous neuromodulators.[5][6] At millimolar concentrations, they may also modulate the redox state of the NMDA receptor complex.[6]
See also
References
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- Organic disulfides
- Excitatory amino acid receptor ligands
- Neurotransmitters