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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

Ice Packs

Storage Temperature

-20°C

Available Sizes

Frequently Asked Questions

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