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FGFR-IN-8
SKU
HY-150652-Get quote
Category Reference compound
Tags Apoptosis;FGFR, Apoptosis;Protein Tyrosine Kinase/RTK, Cancer
Products Details
Product Description
– FGFR-IN-8 (Compound 17a) is a highly potent and orally active panFGFR inhibitor against wild-type and mutant FGFRs. FGFR-IN-8 shows inhibition with IC50 values of <0.5, 189.1, <0.5, 22.6, <0.5 and 7.30 nM against FGFR1, V564F-FGFR2, N549H-FGFR2, V555M-FGFR3, FGFR3 and FGFR4, respectively. GFR-IN-8 induces cancer cell apoptosis and shows anticancer activities[1].
Web ID
– HY-150652
Shipping
– Room temperature
Applications
– Cancer-Kinase/protease
Molecular Formula
– C27H31Cl2N9O2
References
– [1]Ryu S, et al. Identification of Pyridinyltriazine Derivatives as Potent panFGFR Inhibitors against Gatekeeper Mutants for Overcoming Drug Resistance. J Med Chem. 2022 Apr 28;65(8):6017-6038.
CAS Number
– 2640217-64-5
Molecular Weight
– 584.50
SMILES
– CC(N1CCC(N2N=CC(NC3=NC(C4=CC=CN=C4NC5=C(Cl)C(OC)=CC(OC)=C5Cl)=NC=N3)=C2)CC1)C
Clinical Information
– No Development Reported
Research Area
– Cancer
Solubility
– 10 mM in DMSO
Target
– Apoptosis;FGFR
Isoform
– FGFR1;FGFR2;FGFR3;FGFR4
Pathway
– Apoptosis;Protein Tyrosine Kinase/RTK
Product type
– Reference compound
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