Chemical Name: 4-[[[5-Bromo-2-[[3-methyl-1-(2,2,2-trifluoroethyl)pyrazol-4-yl]amino]pyrimidin-4-yl]amino]methyl]benzenesulfonamide
Highly selective TBK1 inhibitor
Molekulargewicht:
520.33
Reinheit:
98% by HPLC NMR (Conforms)
Formulierung:
Beige solid
CAS Nummer:
[2361659-62-1]
Formel:
C17H17BrF3N7O2S
Anwendungsbeschreibung:
Highly selective and potent (avg. pIC50 = 6.8 versus recombinant TBK1) inhibitor of Tank-binding Kinase-1 (TBK1) with higher affinity for unactivated TBK1. It inhibited phosphorylation of IRF3 (pIC50 = 6.0), inhibited the release of IFNa from human PBMCs (pIC50 = 6.1), and inhibited IFNb secretion from THP-1 cells (pIC50 = 5.8 dsDNA virus, 6.3 cGAMP stilmulated cells).
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