LHQ766

LHQ766 is a highly selective, orally active, covalent FGFR2 inhibitor with an IC50 of 7.3 nM. LHQ766 significantly suppresses phosphorylation of FGFR2 and its downstream signaling molecules FRS2-a, Akt and ERK1/2. LHQ766 selectively suppresses the proliferation of FGFR2-driven cancer cells.

For research use only. We do not sell to patients.

  • Formula: C28H27F2N5O3
  • Molecular Weight:519.54
  • Storage:

    Please store the product under the recommended conditions in the Certificate of Analysis.

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All Akt Isoforms

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All ERK Isoforms

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