L-Glutathione reduced
SIAL/G6529 - BioXtra, ≥98.0%
Synonym: γ-L-Glutamyl-L-cysteinyl-glycine; GSH
CAS Number: 70-18-8
Empirical Formula (Hill Notation): C10H17N3O6S
Molecular Weight: 307.32
EC Number: 200-725-4
MDL Number: MFCD00065939
Linear Formula: H2NCH(CO2H)CH2CH2CONHCH(CH2SH)CONHCH2CO2H
Product Type: Chemical
anion traces | sulfate (SO42-): ≤0.05% |
assay | ≥98.0% |
cation traces | Al: ≤0.0005% |
Ca: ≤0.02% | |
Cu: ≤0.0005% | |
Fe: ≤0.001% | |
K: ≤0.005% | |
Mg: ≤0.001% | |
Na: ≤0.005% | |
NH4+: ≤0.05% | |
Pb: ≤0.001% | |
Zn: ≤0.0005% | |
color | white |
form | powder |
ign. residue | ≤0.1% |
impurities | ≤0.02% Phosphorus (P) |
≤0.1% Insoluble matter | |
InChI | 1S/C10H17N3O6S/c11-5(10(1 |
InChI key | RWSXRVCMGQZWBV-WDSKDSINSA |
mp | 192-195 °C (dec.) (lit.) |
product line | BioXtra |
Quality Level | 200 |
SMILES string | N[C@@H](CCC(=O)N[C@@H](CS |
solubility | H2O: 0.1 M, clear, colorless |
storage temp. | 2-8°C |
Amino Acid Sequence: | γ-Glu-Cys-Gly |
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, 25 g in poly bottle |
RIDADR | NONH for all modes of transport |
WGK Germany | WGK 2 |
Flash Point(F) | Not applicable |
Flash Point(C) | Not applicable |
Purity | ≥98.0% |
mp | 192-195 °C (dec.) (lit.) |
Storage Temp. | 2-8°C |
UNSPSC | 12352209 |