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Auranofin

Cat. No. M3178

All AbMole products are for research use only, cannot be used for human consumption.

Auranofin Structure
Synonym:

SKF-39162

Size Price Availability Quantity
10mM*1mL in DMSO USD 60 In stock
1mg USD 21 In stock
5mg USD 39 In stock
10mg USD 62 In stock
25mg USD 119 In stock
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Quality Control & Documentation
Biological Activity

Auranofin is an inhibitor of thioredoxin reductase (TrxR) (IC50 = 20 nM; Ki = 4 nM for the NADPH-reduced form of human cytosolic TrxR). Auranofin induced the mitochondrial permeability transition via inhibition of mitochondrial TrxR. Auranofin also exhibits anti-inflammatory and immunosuppressive activities. Auranofin inhibits 5-lipoxygenase at high concentrations and stimulates LTA hydrolase at low concentrations.

Chemical Information
Molecular Weight 678.48
Formula C20H34AuO9PS
CAS Number 34031-32-8
Solubility (25°C) DMSO 40 mg/mL (Need ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Kim NH, et al. Immunology. Auranofin blocks interleukin-6 signalling by inhibiting phosphorylation of JAK1 and STAT3.

[2] Rigobello MP, et al. Br J Pharmacol. Induction of mitochondrial permeability transition by auranofin, a gold(I)-phosphine derivative.

[3] Gromer S, et al. J Biol Chem. Human placenta thioredoxin reductase. Isolation of the selenoenzyme, steady state kinetics, and inhibition by therapeutic gold compounds.

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Keywords: Auranofin, SKF-39162 supplier, Anti-infection, inhibitors, activators

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