FGFR-IN-4

FGFR-IN-4

• CAS Number: 2761211-49-6
• UNSPSC Description: FGFR-IN-4 is a potent inhibitor of FGFR. Fibroblast growth factor receptor (FGFR) is a tyrosine kinase receptor that binds to fibroblast growth factor ligands. FGFR-IN-4 has the potential for the research of cancer diseases (extracted from patent WO2022033532A1, compound 20)[1]. FGFR-IN-4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
• Target Antigen: FGFR
• Type: Reference compound
• Related Pathways: Protein Tyrosine Kinase/RTK
• Applications: Cancer-Kinase/protease
• Field of Research: Cancer
• Assay Protocol: https://www.medchemexpress.com/fgfr-in-4.html
• Solubility: 10 mM in DMSO
• Smiles: C=CC(N1CC[C@@H](C1)N2N=C(C3=C2N=CN=C3N)C#CC4=CC5=C(OC(C6CC6)=N5)C=C4)=O
• Molecular Weight: 439.47
• References & Citations: [1]Haibin Deng, et al. Fgfr and mutation inhibitor thereof, and preparation method therefor and use thereof. Patent WO2022033532A1.
• Shipping Conditions: Room temperature
• Clinical Information: No Development Reported