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Histone Demethylase

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Histone Demethylase

Chemical Structure Cat. No. Product Name CAS No.
KDM5-IN-1 Chemical Structure
 BCP37630 KDM5-IN-1 1628210-26-3
KDM5-IN-1 is a potent, selective and orally bioavailable KDM5 inhibitor.
KDM5-C70 Chemical Structure
 BCP37627 KDM5-C70 1596348-32-1
KDM5-C70 is a JARID1 Histone Demethylases Inhibitor. KDM5-C70 had an antiproliferative effect in myeloma cells, leading to genome-wide elevation of H3K4me3 levels.
CC-90011 besylate Chemical Structure
 BCP33218 CC-90011 besylate 2097523-60-7
CC-90011 is a potent and orally active LSD1 inhibitor. CC-90011 binds to and inhibits LSD1, a demethylase that suppresses the expression of target genes by converting the di- and mono-methylated forms of lysine at position 4 of histone H3 (H3K4) to mono- and unmethylated H3K4, respectively.
OG-L002 hydrochloride Chemical Structure
 BCP25948 OG-L002 hydrochloride 1357298-75-9
OG-L002 HCl is an inhibitor of LSD1.
KDM4D-IN-1 Chemical Structure
 BCP32624 KDM4D-IN-1 2098902-68-0
KDM4D-IN-1 is a new histone lysine demethylase 4D (KDM4D) inhibitor with an IC50 value of 0.41±0.03 μM.
KDOAM-25 Chemical Structure
 BCP31703 KDOAM-25 2230731-99-2
KDOAM-25 is a potent and highly selective KDM5 sub-family of histone lysine demethylases inhibitor with IC50s of 71 nM, 19 nM, 69 nM, 69 nM for KDM5A, KDM5B, KDM5C, KDM5D, respectively. KDOAM-25 increases global H3K4 methylation at transcriptional start sites and impairs proliferation in multiple myeloma MM1S cells.
GSK-467 Chemical Structure
 BCP30840 GSK-467 1628332-52-4
GSK467 is a potent and selective inhibitor of KDM5 (also known as JARID1). GSK467 exploits unique binding modes.
T-3775440 Chemical Structure
 BCP30535 T-3775440 1422620-34-5
T-3775440 is a novel potent, selecitve, irreversible LSD1 inhibitor with IC50 of 2.1 nM.
T-3775440 hydrochloride Chemical Structure
 BCP30534 T-3775440 hydrochloride 1422535-52-1
T-3775440 hydrochloride is a potent, selecitve, irreversible LSD1 inhibitor.
Corin Chemical Structure
 BCP30529 Corin 1808113-09-8
Corin is a dual inhibitor of histone lysine specific demethylase (LSD1) and histone deacetylase (HDAC), with a Ki(inact) of 110 nM for LSD1 and an IC50 of 147 nM for HDAC1.
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