FY-56 是一种高效的具有选择性LSD1/KDM1A抑制剂 (IC50=42 nM)，比 MAO-A/B 具有高选择性. FY-56 诱导 MOLM-13 和 MV4-11 细胞分化，具有急性髓系白血病 AML 研究潜力。

FY-56 is a highly potent and selective LSD1/KDM1A inhibitor ( IC 50 =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].

C23H19FN2O3

390.41

(< 1 mg/ml refers to the product slightly soluble or insoluble )
Powder: -20°C for 3 years
In solvent: -80°C for 2 years