CH5183284

CH5183284

CAT N°: 17120
Price:

From 74.00 62.90

CH5183284 is a potent, selective inhibitor of the kinase activity of fibroblast growth factor receptors (FGFRs) 1, 2, and 3 (IC50s = 9.3, 7.6, and 22 nM, respectively).{27812} It less potently inhibits FGFR4 and platelet-derived growth factor receptor ? (IC50s = 290 and 560 nM, respectively) and displays IC50 values greater than 1 µM for a diverse panel of tyrosine and serine/threonine kinases.{27812} CH5183284 is effective against FGFR2 containing the gatekeeper mutation V564F.{27812} Moreover, it inhibits the growth of cancer cells expressing FGFR genetic alterations both in vitro and in xenograft mouse models.{27812}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • [5-amino-1-(2-methyl-1H-benzimidazol-6-yl)-1H-pyrazol-4-yl]-1H-indol-2-yl-methanone
  • Correlated keywords
    • biochemical inhibitor receptor biochemistry protein kinase signal transduction cancer inhibit CH-5183284 potent selective fibroblast growth factor FGFR1 FGFR2 FGFR3 FGFR4 FGFR platelet-derived ? tyrosine serine/threonine gatekeeper mutation V564F cell genetic alteration in vitro xenograft mouse model
  • Product Overview:
    CH5183284 is a potent, selective inhibitor of the kinase activity of fibroblast growth factor receptors (FGFRs) 1, 2, and 3 (IC50s = 9.3, 7.6, and 22 nM, respectively).{27812} It less potently inhibits FGFR4 and platelet-derived growth factor receptor ? (IC50s = 290 and 560 nM, respectively) and displays IC50 values greater than 1 µM for a diverse panel of tyrosine and serine/threonine kinases.{27812} CH5183284 is effective against FGFR2 containing the gatekeeper mutation V564F.{27812} Moreover, it inhibits the growth of cancer cells expressing FGFR genetic alterations both in vitro and in xenograft mouse models.{27812}

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