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BI605906

Catalog No. T14567   CAS 960293-88-3

BI605906 is an inhibitor of IKKβ. When assayed at 0.1 mM ATP, the IC50 value is 380 nM.

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BI605906 Chemical Structure
BI605906, CAS 960293-88-3
Pack Size Availability Price/USD Quantity
2 mg 5 days $ 87.00
25 mg 6-8 weeks $ 674.00
50 mg 6-8 weeks $ 876.00
100 mg 6-8 weeks $ 1,320.00
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Biological Description
Chemical Properties
Storage & Solubility Information
Description BI605906 is an inhibitor of IKKβ. When assayed at 0.1 mM ATP, the IC50 value is 380 nM.
Targets&IC50 ATP (0.1 mM):, IKKβ:380 nM
In vitro BI605906 is an inhibitor of IKKβ with improved selectivity. BI605906 partially inhibits the IL-1-stimulated activation of IKKε/TBK1[1]. BI605906 inhibits IKKβ in vitro with an IC50 value of 380 nM when assayed at 0.1 mM ATP. The only other protein kinase that is inhibited of over 100 tested, which include IKKα, IKKε and TBK1, is the insulin-like growth factor 1 (IGF1) receptor (IC50=7.6 μM). TNF-α-dependent expression of CINC-1/CXCL1, CXCL2, IL-1β, and IL-6 is strongly inhibited by both Metformin and BI605906 (10 μM)[2]. In primary mouse hepatocytes, Metformin treatment for 3 hours suppresses TNFα-induced degradation of the NF-κB negative regulator IκB, while modulating AMPK and MTOR signaling in a dose-dependent manner. The magnitude of the effect on IκB is comparable with BI605906. Unlike Metformin, BI605906 (10 μM ) does not suppress signaling downstream of mTOR nor does it activate AMPK.
Molecular Weight 432.51
Formula C17H22F2N4O3S2
CAS No. 960293-88-3

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 100 mg/mL (231.21 mM)

TargetMolReferences and Literature

1. Clark K, et al. Novel cross-talk within the IKK family controls innate immunity. Biochem J. 2011 Feb 15;434(1):93-104. 2. Cameron AR, et al. Anti-Inflammatory Effects of Metformin Irrespective of Diabetes Status. Circ Res. 2016 Aug 19;119(5):652-65.

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Keywords

BI605906 960293-88-3 NF-Κb IκB/IKK BI 605906 BI-605906 inhibitor inhibit

 

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