Product Description
ALW-II-41-27 is a Eph family tyrosine kinase inhibitor with an IC50 of 11 nM for Eph2.
IC50 & Target: IC50: 11 nM (Eph2)[1]
In Vitro: ALW-II-41-27 inhibits Ba/F3 cells transformed with Tel fusions of EphA3, Kit, Fms, KDR, FLT1, FGR, Src, Lyn, Bmx, and Bcr-Abl with an EC50 below 500 nM. ALW-II-41-27 exhibits cross reactivity with Bcr-Abl. ALW-II-41-27 inhibits b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2, EphB3, Frk, Kit, Lck, p38α, p38β, PDGFRα, PDGFRβ, and Raf1 and many more demonstrating how introduction of the thiophene group can have a tremendous impact on kinase selectivity[1].
Information
CAS No1186206-79-0
FormulaC32H32F3N5O2S
Clinical Informationclinicalinformation
PathwayProtein Tyrosine Kinase/RTK
TargetEphrin Receptor
Specifications
Purity / Grade>98%
SolubilityDMSO : ≥ 47 mg/mL (77.34 mM)
Smilessmiles
Misc Information
Alternative NamesEph receptor tyrosine kinase inhibitor
Observed Molecular Weight607.69