2143104-11-2

EGFR T790M/FAK-IN-2 Chemical Structure
2143104-11-2

Chemical Structure

EGFR T790M/FAK-IN-2

  • CAS No.: 2143104-11-2
  • Formula:C25H28ClN7O3
  • Molecular Weight:510.00

IUPAC Name: 2-((5-chloro-2-((3-methyl-4-(2-morpholinoacetamido)phenyl)amino)pyrimidin-4-yl)amino)-N-methylbenzamide

InChIKey: IWCUHRIIUCIMLP-UHFFFAOYSA-N

SMILES: O=C(NC)C=1C=CC=CC1NC2=NC(=NC=C2Cl)NC3=CC=C(NC(=O)CN4CCOCC4)C(=C3)C

Biological Activity: EGFR T790M/FAK-IN-2 is an orally active dual FAK and EGFRT790M kinase inhibitor, with an IC50 of 1.03 nM against FAK and an IC50 of 3.89 nM against EGFRT790M. EGFR T790M/FAK-IN-2 exerts antiproliferative effects in drug-resistant cancer cells overexpressing FAK, inducing apoptosis and cell cycle arrest. EGFR T790M/FAK-IN-2 exhibits antitumor activity in a pancreatic cancer xenograft mouse model. EGFR T790M/FAK-IN-2 can be used for the research of pancreatic cancer, breast cancer and non-small cell lung cancer[1].

Cat. No. Product Name Purity Description Pricing
HY-183120
EGFR T790M/FAK-IN-2 EGFR T790M/FAK-IN-2 is an orally active dual FAK and EGFRT790M kinase inhibitor, with an IC50 of 1.03 nM against FAK and an IC50 of 3.89 nM against EGFRT790M. EGFR T790M/FAK-IN-2 exerts antiproliferative effects in drug-resistant cancer cells overexpressing FAK, inducing apoptosis and cell cycle arrest. EGFR T790M/FAK-IN-2 exhibits antitumor activity in a pancreatic cancer xenograft mouse model. EGFR T790M/FAK-IN-2 can be used for the research of pancreatic cancer, breast cancer and non-small cell lung cancer.
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