OG-L002 is a potent and highly selective LSD1 inhibitor with an IC50 of 0.02 µM. OG-L002 is a potent monoamine oxidases (MAO) inhibitor with IC50s of 1.38 µM and 0.72 µM for MAO-A and MAO-B, respectively. OG-L002 potently inhibits the expression of HSV IE genes[1].
Molecular Weight:
225.29
Purity:
99.55
CAS Number:
[1357302-64-7]
Formula:
C15H15NO
Target:
Histone Demethylase,HSV,Monoamine Oxidase
Application Notes:
MCE Product type: Reference compound1
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