MW 437.9 Da, Purity >98%. Potent, selective (IC50 = 13 nM) and reversible inhibitor of the histone demethylase LSD1 (KDM1A). No activity against MAO-A, MAO-B, lactate dehydrogenase and glucose oxidase.
View Alternative Names
AOF2, Amine oxidase (flavin containing) domain 2, Amine oxidase, flavin containing, 2, BHC110, BRAF35-HDAC complex protein BHC110, BRAF35/HDAC complex, 110-kD subunit, CPRF, EC1, FAD-binding protein BRAF35-HDAC complex, 110 kDa subunit, Flavin-containing amine oxidase domain-containing protein 2, KDM 1, KDM1A_HUMAN, KIAA0601, LSD 1, Lysine (K) specific demethylase 1, Lysine (K) specific demethylase 1A, Lysine demethylase 1A, Lysine-specific demethylase 1, Lysine-specific demethylase 1A, Lysine-specific histone demethylase 1, Lysine-specific histone demethylase 1A
- Chemical Structure
Supplier Data
Chemical Structure - SP-2509, LSD1 inhibitor (AB254459)
2D chemical structure image of ab254459, SP-2509, LSD1 inhibitor
Product details
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