Substance
ID:367389
Names and Identifiers
IUPAC name
(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)carbamoyl]-2-sulfanylethyl]carbamoyl}butanoic acid
IUPAC Traditional name
glutathione
Synonyms
5-L-谷氨酰-L-半胱氨酰甘氨酸γ-L-Glutamyl-L-cysteinyl-glycineL-还原型谷胱甘肽GSHL-Glutathione reduced
Registration numbers
Beilstein Number
MDL Number
EC Number
CAS Number
PubChem SID
Properties
Physical Property
Melting Point
192-195 °C (dec.)(lit.)
Safety Information
RTECS
MC0556000
Storage Temperature
2-8°C
German water hazard class
2
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
MSDS Link
Product Information
Linear Formula
H2NCH(CO2H)CH2CH2CONHCH(CH2SH)CONHCH2CO2H
Quality Level
PREMIUM
Purity
≥98.0%
Molecule Details
Amino Acid Sequence
γ-Glu-Cys-Gly
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Application
May be used at 5-10 mM to elute glutathione S-transferase (GST) from glutathione agarose.
Biochem/physiol Actions
Endogenous antioxidant that plays a major role in reducing reactive oxygen species formed during cellular metabolism and the respiratory burst. Glutathione-S-transferase catalyzes the formation of glutathione thioethers with xenobiotics, leukotrienes, and other molecules that have an electrophilic center. Glutathione also forms disulfide bonds with cysteine residues in proteins. Via these mechanisms, it can have the paradoxical effect of reducing the efficacy of anti-cancer agents.
Packaging
1, 5, 10, 25, 50, 100, 250, 500 g in poly bottle
300 mg in poly bottle
10 mg in autosmp vl
γ-Glu-Cys-Gly
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Application
May be used at 5-10 mM to elute glutathione S-transferase (GST) from glutathione agarose.
Biochem/physiol Actions
Endogenous antioxidant that plays a major role in reducing reactive oxygen species formed during cellular metabolism and the respiratory burst. Glutathione-S-transferase catalyzes the formation of glutathione thioethers with xenobiotics, leukotrienes, and other molecules that have an electrophilic center. Glutathione also forms disulfide bonds with cysteine residues in proteins. Via these mechanisms, it can have the paradoxical effect of reducing the efficacy of anti-cancer agents.
Packaging
1, 5, 10, 25, 50, 100, 250, 500 g in poly bottle
300 mg in poly bottle
10 mg in autosmp vl
Molecular Spectra
No Data Available
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References
No Data Available
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