3081622-36-5

ALK/EGFR-IN-4 Chemical Structure
3081622-36-5

Chemical Structure

ALK/EGFR-IN-4

  • CAS No.: 3081622-36-5
  • Formula:C24H29ClN7O4P
  • Molecular Weight:545.96

InChIKey: JPGNRNMUXAFODV-UHFFFAOYSA-N

SMILES: CP(C)(C1=CC=CC=C1NC2=NC(NC3=CC([N+]([O-])=O)=C(N4CCN(C)CC4)C=C3OC)=NC=C2Cl)=O

Biological Activity: ALK/EGFR-IN-4 is an EGFR and ALK inhibitor (EGFRL858R/T790M/C797S (IC50 1.76 nM), EGFRL858R/T790M (2.97 nM), wild-type EGFR (59.35 nM) and ALK (1.95 nM)). ALK/EGFR-IN-4 induces G0/G1 phase arrest and Apoptosis, inhibits DNA synthesis, downregulates Cyclin D1, and inhibits AKT/ERK/STAT3 phosphorylation. ALK/EGFR-IN-4 shows antitumor efficacy in an Osimertinib (HY-15772)-resistant EGFR triple-mutant non-small cell lung cancer xenograft model[1].

Cat. No. Product Name Purity Description Pricing
HY-190486
ALK/EGFR-IN-4 ALK/EGFR-IN-4 is an EGFR and ALK inhibitor (EGFRL858R/T790M/C797S (IC50 1.76 nM), EGFRL858R/T790M (2.97 nM), wild-type EGFR (59.35 nM) and ALK (1.95 nM)). ALK/EGFR-IN-4 induces G0/G1 phase arrest and Apoptosis, inhibits DNA synthesis, downregulates Cyclin D1, and inhibits AKT/ERK/STAT3 phosphorylation. ALK/EGFR-IN-4 shows antitumor efficacy in an Osimertinib (HY-15772)-resistant EGFR triple-mutant non-small cell lung cancer xenograft model.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References