JNJ-38877605 is an orally active ATP-competitive inhibitor of c-Met with an IC50 of 4 nM, 600-fold selective for c-Met than 200 other tyrosine and serine-threonine kinases[1][2]. JNJ-38877605 inhibits c-Met phosphorylation and regulates lipid accumulatio
Molecular Weight:
377.35
Purity:
99.95
CAS Number:
[943540-75-8]
Formula:
C19H13F2N7
Target:
c-Met/HGFR
Application Notes:
Reference compound
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