FY-56 is a highly potent and selective LSD1/KDM1A inhibitor (IC50=42 nM) and exhibits high selectivity over MAO-A/B. FY-56 induces differentiation of MOLM-13 and MV4-11 cell and has the potential for AML research[1].
Molecular Weight:
390.41
Formula:
C23H19FN2O3
Target:
Histone Demethylase
Application Notes:
Reference compound
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