FY-56

• 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