LSD1 Inhibitors

Histone methylation regulates chromatin structure and transcription and maintains an epigenetic state of the cell. Biochemicals that inhibit LSD1 have many applications in biochemical and physiological research. Click on the product name to view detailed information such as the chemical structure and specific chemical properties for each of our LSD1 Inhibitors. In stock LSD1 Inhibitors are available for immediate shipping.

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PRODUCT NAME/Application CAS Catalog # QUANTITY Price Citations RATING
Tranylcypromine is an irreversible inhibitor of MAO and inhibitor of histone demethylation
13492-01-8 sc-200572
1 g
5 g
trans 2-Phenylcyclopropylamine Hydrochloride
trans 2-Phenylcyclopropylamine Hydrochloride is a non-selective inhibitor of MAO
1986-47-6 sc-208452
250 mg
1 g
RN 1 dihydrochloride
RN 1 dihydrochloride is an LSD1 inhibitor
1781835-13-9 sc-397054
10 mg
CAS: 1423715-09-6, MF: C19H20ClN3O5S, MW: 437.9
1423715-09-6 sc-492604
5 mg
GSK LSD1 Dihydrochloride
GSK LSD1 Dihydrochloride is an anti cancer compound that is irreversible mechanism-based inhibitor of LSD1
1431368-48-7 (free base) sc-490345
5 mg
OG-L002 is OG-L002 is a potent and specific LSD1 inhibitor with IC50 of 20 nM in a cell-free assay, exhibiting 36- and 69-fold selectivity over MAO-B and
1357302-64-7 sc-478221
5 mg

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