FGFR-IN-14
FGFR-IN-14 (compound 10h) is a pan-FGFR inhibitor. FGFR-IN-14 inhibits FGFR1, FGFR2, FGFR3 and FGFR2 V564F gatekeeper mutant with IC50s of 46, 41, 99, and 62 nM, respectively. FGFR-IN-14 strongly suppresses NCI-H520 lung cancer cells, SNU-16 and KATO III gastric cancer cells proliferation with IC50s of 19, 59, and 73 nM, respectively[1].
Product Specifications
UNSPSC
12352005
Target
FGFR
Type
Reference compound
Related Pathways
Protein Tyrosine Kinase/RTK
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/fgfr-in-14.html
Smiles
CC(N1)=NC2=C1C=C(F)C(C#CC3=NN(CC4=CC=CC(NC(C=C)=O)=C4)C(N)=C3C(N)=O)=C2F
Molecular Formula
C24H19F2N7O2
Molecular Weight
475.45
References & Citations
[1]Deng W, et al. Design, synthesis and biological evaluation of 5-amino-1H-pyrazole-4-carboxamide derivatives as pan-FGFR covalent inhibitors. Eur J Med Chem. 2024 Jun 9;275:116558.
Shipping Conditions
Room temperature
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Frequently Asked Questions
More Discoveries
Explore Other Products
Browse additional items from our catalog
VAng-Cr5261-50gEcoli 50 µg (E. coli)
Recombinant Klebsiella Pneumoniae pyrF Protein (aa 1-245)
Sign In for Pricing
View Details K2730003 1.0 µg DNA
ZNF733 sgRNA CRISPR Lentivector (Human) (Target 2)
Sign In for Pricing
View Details