FGFR1 inhibitor-9
Product Specifications
Target
FGFR
Related Pathways
Tyrosine Kinase/Adaptors|||Angiogenesis
Bioactivity
FGFR1 inhibitor-9 (Compound 7) is a potent FGFR1 inhibitor with an IC50 of 0.85 nM, targeting the ATP-binding pocket of FGFR1 and demonstrating anticancer activity [1].
Molecular Formula
C27H20ClNO5
Molecular Weight
473.9
Shipping Conditions
Cool pack
Storage Temperature
-20°C
Available Sizes
Curated Selection
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items
MBS6208397-01 0.1 mL
RUNX1 (Runt-Related Transcription Factor 1, AML1, AML1-EVI-1, AMLCR1, CBFA2, EVI-1, PEBP2aB) (MaxLight 490)
Ask
View Details MBS6208397-02 5x 0.1 mL
RUNX1 (Runt-Related Transcription Factor 1, AML1, AML1-EVI-1, AMLCR1, CBFA2, EVI-1, PEBP2aB) (MaxLight 490)
Ask
View Details 