Description
A TAM family kinase inhibitor (IC50s = 5, 8, and 29 nM for Mer, Tyro3, and Axl, respectively); selective for TAM family kinases over a panel of 456 kinases at 1 μM, but does inhibit Met, Aurora B, LCK, and Src (IC50s = 35, 36, 51, and 338 nM, respectively); inhibits GAS6-induced suppression of proliferation and IFN-γ production in NKG2D-activated NK cells; adoptive transfer of treated NK cells decreases tumor growth but not metastasis in a B16/F10 murine melanoma model; reduces the number of metastases in B16/F10 murine melanoma and 4T1 murine mammary carcinoma models in an NK cell-dependent manner at 20 mg/kg, i.p.
Formal name: N-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-3-fluorophenyl]-4-ethoxy-1-(4-fluoro-2-methylphenyl)-1H-pyrazole-3-carboxamide
Synonyms:
Molecular weight: 560.6
CAS: 1361030-48-9
Purity: ≥98%
Formulation: A crystalline solid