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BAY 11-7082

Cat. No. M2040

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

BAY 11-7082 Structure
Synonym:

BAY 11-7821; NF-κB inhibitor 13

Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
10mM*1mL in DMSO USD 58 In stock
5mg USD 50 In stock
10mg USD 63 In stock
25mg USD 110 In stock
50mg USD 202 In stock
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Quality Control & Documentation
Biological Activity

BAY 11-7082 (BAY 11-7821) is an irreversible inhibitor of TNF-α-stimulated IκBα phosphorylation. BAY 11-7082 selectively and irreversibly inhibits NF-κB activation by blocking TNF-α-induced phosphorylation of IκB-α without affecting constitutive IκB-α phosphorylation. BAY 11-7082 inhibits the TNF-α-induced surface expression of adhesion molecules ICAM-1, VCAM-1, and E-selectin in human endothelial cells with IC50 values of 5-10 µM. BAY 11-7082 also reversibly activates MAP kinases and stimulates apoptosis. BAY 11-7082 rapidly and efficiently reduced the DNA binding of NF-kappaB in HTLV-I-infected T-cell lines and down-regulated the expression of the antiapoptotic gene, Bcl-x(L), regulated by NF-kappaB, whereas it had little effect on the DNA binding of another transcription factor, AP-1.

Furthermore, BAY 11-7082- induced apoptosis of primary ATL cells was more prominent than that of normal peripheral blood mononuclear cells, and apoptosis of these cells was also associated with down-regulation of NF-kappaB activity.

Product Citations
Customer Product Validations & Biological Datas
Source Biochem J (2013). Figure 2. Bay 11-7082
Method immunoblotting
Cell Lines human IL-1R cells
Concentrations 15 μM
Incubation Time 1 h
Results BAY 11-7082 completely suppressed the LPS-stimulated and IL-1-stimulated phosphorylation of the activation loop of IKKβ.
Protocol (for reference only)
Cell Experiment
Cell lines HT29 cells
Preparation method HT29 cells (40,000) were seeded on 8-chamber glass slides. After adherence, cells were either pretreated for 30 min with Bay 11-7082 (30 µM) or TPCA-1 (20 µM), or remained untreated.
Concentrations 30 µM
Incubation time 30 min
Animal Experiment
Animal models Female SCID/beige mice
Formulation 1% DMSO
Dosages 20 mg/kg
Administration Intraperitoneal administration
Chemical Information
Molecular Weight 207.25
Formula C10H9NO2S
CAS Number 19542-67-7
Solubility (25°C) DMSO ≥ 40 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Gastonguay A, et al. Cancer Biol Ther. The role of Rac1 in the regulation of NF-κB activity, cell proliferation, and cell migration in non-small cell lung carcinoma.

[2] Goffi F, et al. Neurosci Lett. The inhibitor of I kappa B alpha phosphorylation BAY 11-7082 prevents NMDA neurotoxicity in mouse hippocampal slices.

[3] Mori N, et al. Blood. Bay 11-7082 inhibits transcription factor NF-kappaB and induces apoptosis of HTLV-I-infected T-cell lines and primary adult T-cell leukemia cells.

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  Catalog
Abmole Inhibitor Catalog




Keywords: BAY 11-7082, BAY 11-7821; NF-κB inhibitor 13 supplier, IκB/IKK, inhibitors, activators

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