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Medchemexpress LLC N-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-3-fluorophenyl]-3-(4-fluorophenyl)-1,2,3,4-tetrahydro-1-(1-meth | 1437321-24-8 | 99.6% | 588.56 g/mol | C31H26F2N4O6 | 200 MG
SDP

Catalog No. 5000212171
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CEP-40783 (RXDX-106) is a potent, selective, orally available small-molecule inhibitor of the receptor tyrosine kinases AXL and c-Met. It exhibits low-nanomolar inhibitory activity (AXL IC50 = 7 nM; c-Met IC50 = 12 nM) and is supplied as a high-purity solid for research use.

  • Potent inhibition of AXL and c-Met at low-nanomolar concentrations.
  • Orally available small-molecule scaffold suitable for in vitro and in vivo studies.
  • High purity suitable for biochemical and cellular assays.
  • Characterized molecular formula and molecular weight for formulation work.
  • Provided with safety and handling documentation for laboratory use.

Catalog No. 50-002-12171 Supplier Medchemexpress LLC Supplier No. HY100946200MG
May include imposed supplier surcharges.
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CEP-40783 (RXDX-106) is a potent, selective, orally available small-molecule inhibitor of the receptor tyrosine kinases AXL and c-Met. It exhibits low-nanomolar inhibitory activity (AXL IC50 = 7 nM; c-Met IC50 = 12 nM) and is supplied as a high-purity solid for research use.

  • Potent inhibition of AXL and c-Met at low-nanomolar concentrations.
  • Orally available small-molecule scaffold suitable for in vitro and in vivo studies.
  • High purity suitable for biochemical and cellular assays.
  • Characterized molecular formula and molecular weight for formulation work.
  • Provided with safety and handling documentation for laboratory use.

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