Background Information:

A potent, selective (>1000-fold more selective than other 208
kinases), orally bioavailable c-Met kinase inhibitor with Ki at low nM.

Reference:

1. S. L. Timofeevski, et al, Enzymatic Characterization of c-Met
Receptor Tyrosine Kinase Oncogenic Mutants and Kinetic Studies with
Aminopyridine and Triazolopyrazine Inhibitors, Biochemistry, 2009, 48
(23), 5339–5349.

APIM050224: PF-04217903

CAS No.: 1159490-85-3.
Molecular Formula: C₁₉H₁₆N₈O.
Molecular Weight: 372.38.
Purity: ≥ 99% (HPLC).
QC: LC/MS, ¹HNMR.
Solubility: Soluble in DMSO, water (pH < 7).
Storage: Store at 0°C (short term), -20°C (long term), desiccated.