LHQ766
LHQ766 is a highly selective and orally effective covalent FGFR2 inhibitor with an IC50 of 7.3 nM. It significantly inhibits the phosphorylation of FGFR2 and its downstream signaling molecules FRS2-a, Akt, and ERK1/2. LHQ766 selectively suppresses the proliferation of cancer cells driven by FGFR2.
Product Specifications
Storage Conditions
-20°C
Notes
For research use only.
Available Sizes
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