FY-56
Product Specifications
Target
Others|||Histone Demethylase
Related Pathways
Others|||Chromatin/Epigenetic
Bioactivity
FY-56, a highly potent and selective inhibitor of LSD1/KDM1A with an IC50 value of 42 nM, demonstrates significant selectivity over MAO-A/B. This compound effectively induces differentiation in MOLM-13 and MV4-11 cells, showing promise for acute myeloid leukemia (AML) research [1].
Molecular Formula
C23H19FN2O3
Molecular Weight
390.41
Shipping Conditions
Cool pack
Storage Temperature
-20°C
Available Sizes
Curated Selection
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