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Product Description
QL47 is a potent, selective and irreversible BTK kinase inhibitor with IC50 of 7 nM.
IC50 Value: 7 nM
Target: Btk
in vitro: QL47 inhibits BTK kinase activity with an IC50 of 7 nM, inhibits autophosphorylation of BTK on Tyr223 in cells with an EC50 of 475 nM and inhibits phosphorylation of a downstream effector PLCγ2 (Tyr759) with an EC50 of 318 nM. In Ramos cells QL47 induces a G1 cell cycle arrest which is associated with pronounced degradation of BTK protein. QL47 inhibits the proliferation of B-cell lymphoma cancer cell lines at submicromolar concentrations [1].
in vivo: N/A
Information
CAS No1469988-75-7
FormulaC27H21N5O2
Clinical Informationclinicalinformation
PathwayProtein Tyrosine Kinase/RTK
TargetBtk
Specifications
Purity / Grade>98%
Solubility10 mM in DMSO
Smilessmiles
Misc Information
Alternative NamesBTK Inhibitor
Observed Molecular Weight447.49
related data
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