Description
An inhibitor of Mer kinase (IC50 = 4.3 nM); selective for Mer over Axl and TYRO3 (IC50s = 360 and 250 nM, respectively); inhibits phosphorylation of Mer in 697 B-ALL cells (IC50 = 21.9 nM); inhibits platelet aggregation and ATP release induced by type I equine fibrillar collagen in isolated human platelet-rich plasma at 3 μM
Formal name: 2-(butylamino)-4-[(trans-4-hydroxycyclohexyl)amino]-N-[[4-(1H-imidazol-1-yl)phenyl]methyl]-5-pyrimidinecarboxamide
Synonyms:
Molecular weight: 463.6
CAS: 1493764-08-1
Purity: ≥98%
Formulation: A crystalline solid