Description
A PDGFR family kinase inhibitor (IC50s = 7.7, 10.5, 2, and 1.2 nM for PDGFRβ, CSF1R, FLT3, and c-Kit, respectively); >30-fold selective for PDGFR family kinases over a panel of 386 kinases, as well as over a panel of 5 CYP enzymes (IC50s = >40 µM); inhibits CSF1R-dependent M-NFS-60 murine leukemia cell proliferation and reduces tumor volume in an FLT3 mutant MV4-11 leukemia mouse xenograft model at 30 mg/kg
Formal name: N-[4-[[[[5-(1,1-dimethylethyl)-3-isoxazolyl]amino]carbonyl]amino]phenyl]-5-[(1-ethyl-2,2,6,6-tetramethyl-4-piperidinyl)oxy]-2-pyridinecarboxamide
Synonyms:
Molecular weight: 562.7
CAS: 1351522-04-7
Purity: ≥98%
Formulation: A crystalline solid