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OG-L002
CAS No. : 1357302-64-7
Biological Activity：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.
Research Area：Infection
Targets：HSV|Monoamine Oxidase|Histone Demethylase
Related Screening Libraries:Bioactive Compound Library Plus;Anti-Infection Compound Library;Epigenetics Compound Library;Neuronal Signaling Compound Library;Histone Modification Research Compound Library;Antiviral Compound Library;Reprogramming Compound Library;Anti-Cancer Metabolism Compound Library;Anti-Parkinson’s Disease Compound Library;Neurodegenerative Disease-related Compound Library;Mitochondria-Targeted Compound Library;Antidepressant Compound Library;
Related Small Molecules:Bomedemstat ditosylate;Isoborneol;PXS-4728A;Vidarabine monohydrate;LSD1/ER-IN-1;PBIT;JQKD82;Hypericin;Simtuzumab;SSAO inhibitor-1;KDOAM-25 citrate;GSK-J1 lithium salt;S2116;5-HT6R/MAO-B modulator 1;Glicoricone;Pritelivir mesylate;Isookanin;LDC4297;MAO-B-IN-1;LOX-IN-3
Trending products：Recombinant Proteins | Bioactive Screening Libraries | Natural Products | Fluorescent Dye | PROTAC | Isotope-Labeled Compounds | Oligonucleotides
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