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EGFR/c-Met-IN-1
SKU
HY-163006-Get quote
Category Reference compound
Tags c-Met/HGFR;EGFR, Cancer, JAK/STAT Signaling;Protein Tyrosine Kinase/RTK
Products Details
Product Description
– EGFR/c-Met-IN-1 (compound TS-41) is a dual-target inhibitor of EGFR/c-Met. The IC50 for inhibiting EGFRL858R and c-Met is 68.1 nM and 0.26 nM respectively. . EGFR/c-Met-IN-1 induces apoptosis and cell cycle arrest in A549-P cells, downregulating the phosphorylation of EGFR, c-Met, and downstream AKT. EGFR/c-Met-IN-1 inhibits tumor growth in vitro and in vivo[1].
Web ID
– HY-163006
Shipping
– Room temperature
Molecular Formula
– C30H25FN6O5
References
– [1]Tang S et al. Design, synthesis, and biological evaluation of 4-(2-fluorophenoxy)-7-methoxyquinazoline derivatives as dual EGFR/c-Met inhibitors for the treatment of NSCLC. Eur J Med Chem. 2023 Nov 15;263:115939.
Molecular Weight
– 568.56
SMILES
– O=C(C1=C(C)N(C)N(C2=CC=CC=C2)C1=O)NC3=CC=C(OC4=C5C=C(NC(C=C)=O)C(OC)=CC5=NC=N4)C(F)=C3
Clinical Information
– No Development Reported
Research Area
– cancer
Solubility
– 10 mM in DMSO
Target
– c-Met/HGFR;EGFR
Pathway
– JAK/STAT Signaling;Protein Tyrosine Kinase/RTK
Product type
– Reference compound
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