Merck
All Photos(5)

G6013

Sigma-Aldrich

L-Glutathione reduced

suitable for cell culture, BioReagent, ≥98.0%, powder

Synonym(s):
γ-L-Glutamyl-L-cysteinyl-glycine, GSH
Linear Formula:
H2NCH(CO2H)CH2CH2CONHCH(CH2SH)CONHCH2CO2H
CAS Number:
Molecular Weight:
307.32
Beilstein:
1729812
Numer EC:
Numer MDL:
Identyfikator substancji w PubChem:
NACRES:
NA.26

linia produktu

BioReagent

Poziom jakości

300

próba

≥98.0%

forma

powder

technique(s)

cell culture | mammalian: suitable

kolor

white

mp

192-195 °C (dec.) (lit.)

rozpuszczalność

H2O: 50 mg/mL

temp. przechowywania

2-8°C

SMILES string

N[C@@H](CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O)C(O)=O

InChI

1S/C10H17N3O6S/c11-5(10(18)19)1-2-7(14)13-6(4-20)9(17)12-3-8(15)16/h5-6,20H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)/t5-,6-/m0/s1

InChI key

RWSXRVCMGQZWBV-WDSKDSINSA-N

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Related Categories

Amino Acid Sequence

γ-Glu-Cys-Gly

Opakowanie

5, 10, 25, 100 g in poly bottle

Zastosowanie

May be used at 5-10 mM to elute glutathione S-transferase (GST) from glutathione agarose.

Działania biochem./fizjol.

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.

Kod klasy składowania

11 - Combustible Solids

WGK

WGK 2

Temperatura zapłonu °F

Not applicable

Temperatura zapłonu °C

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)

Certificate of Analysis

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Certificate of Origin

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