BAY 11-7082 (CAS: 19542-67-7)
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SKU-Pack Size | Availability | Size | Price | |
EBC51044-1ML | In Stock | 1mL(10mM in DMSO) | £59.40 | |
EBC51044-2MG | In Stock | 2mg | £42.90 | |
EBC51044-10MG | In Stock | 10mg | £70.40 | |
EBC51044-25MG | In Stock | 25mg | £114.40 | |
EBC51044-50MG | In Stock | 50mg | £202.40 |
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CUlabSciences | Phone:+44 (0) 1232 330008 | |
Cambridge House St Thomas' Place Ely, | E-mail:sales@culabsciences.co.uk | |
United Kingdom | Cambridge CB27 9RD UK | Web:www.culabsciences.co.uk |
Product Information | |||||||||||||||||||||
Synonym(s) | BAY 11-7821 | ||||||||||||||||||||
Chemical Name | (E)-3-(4-methylphenyl)sulfonylprop-2-enenitrile | ||||||||||||||||||||
Application | BAY 11-7082 is an anti-inflammatory agent and NFκB inhibitor | ||||||||||||||||||||
CAS Number | 19542-67-7 | ||||||||||||||||||||
Purity | ≥99.0% | ||||||||||||||||||||
Molecular Weight | 207.25 | ||||||||||||||||||||
Molecular Formula | C₁₀H₉NO₂S | ||||||||||||||||||||
SMILES | N#C/C=C/S(=O)(C1=CC=C(C)C=C1)=O | ||||||||||||||||||||
Target & IC50 | USP7: IC50 = 0.19 μM NF-kappa-B p65 subunit nuclear translocation: IC50 = 3 μM |
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Solubility | DMSO: 20.7 mg/mL (100 mM)
Ethanol: 5.2 mg/mL (25 mM) |
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Preparing Stock Solutions |
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Shipping | Gel Pack | ||||||||||||||||||||
Storage | Store at -20°C | ||||||||||||||||||||
Research Use | For Research Use Only. Not Intended for Diagnostic Or Therapeutic Use. |
Product Description | |
BAY 11-7082, a potential anti-inflammatory agent, is an irreversible inhibitor of IKK α and phosphorylation of cytokine-inducible IκBα (nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-α, NFKBIA; IC50=10 μM). In intact HUVECs, it inhibits TNFα-induced phosphorylation and degradation of IκBa (NFKBIA) without affecting constitutive phosphorylation. Inhibition of ιBα phosphorylation and degradation results in the inactivation of NFκB and thereby inhibits the expression of endothelial-leukocyte adhesion molecules: E-selectin, VCAM-1 and ICAM-11. BAY 11-7082 has also demonstrated stimulation of the stress-activated protein kinases, p38 and JNK-1. |
Specific Protocols | |