OG-L002
OG-L002 is a potent and selective LSD1 inhibitor with an IC50 of 20 nM, demonstrating 69-fold and 36-fold selectivity against MAO-A and MAO-B, respectively. It is a valuable chemical probe for studying epigenetic regulation in cancer research and has been utilized in both cellular and animal models of leukemia and solid tumors.
Product Specifications
CAS Number
1357302-64-7
Product Name Alternative
Herpes simplex virus, MAO, MAO-A, MAO-B, MonoamineOxidase, Monoamine Oxidase, monoamine, HistoneDemethylase, Histone Demethylase, HSV, OG L002, OG-L 002, OGL002, OG-L002, OG-L-002, oxidases, LSD1, inhibit, Inhibitor
Field of Research
Epigenetics & Chromatin, Infectious Disease & Virology, Neuroscience
Purity
97.05% (May vary between batches)
Solubility
10% DMSO+40% PEG300+5% Tween 80+45% Saline:1 mg/mL (4.44 mM) ; Ethanol:16 mg/mL (71.02 mM) ; H2O:< 1 mg/mL (insoluble or slightly soluble) ; DMSO:55 mg/mL (244.13 mM)
Smiles
N[C@H]1C[C@@H]1c1ccc (cc1) -c1cccc (O) c1
Molecular Formula
C15H15NO
Molecular Weight
225.29
Storage Conditions
-20°C
Notes
For research use only.
Available Sizes
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