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Histone Demethylase

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Histone Demethylase

结构式 货号 产品名称 CAS号
Bomedemstat ditosylate 结构式
BCP44102 Bomedemstat ditosylate 1990504-72-7
Bomedemstat is a lysine-specific histone demethylase 1 (LSD1) inhibitor with antineoplastic activity.
Pulrodemstat 结构式
BCP44101 Pulrodemstat 1821307-10-1
Pulrodemstat 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. CC-90011 exhibits potent on-target induction of cellular differentiation in acute myeloid leukemia (AML) and small cell lung cancer (SCLC) cell lines, and antitumor efficacy in patient-derived xenograft (PDX) SCLC models.
PFI-90 结构式
BCP42958 PFI-90 53995-62-3
PFI-90 is a selective inhibitor of the histone demethylase KDM3B.
DDP-38003 2HCl 结构式
BCP39854 DDP-38003 2HCl 1831167-98-6
DDP-38003 2HCl is an orally available inhibitor of histone lysine-specific demethylase 1A (LSD1).
KDM5-IN-1 结构式
BCP37630 KDM5-IN-1 1628210-26-3
KDM5-IN-1 is a potent, selective and orally bioavailable KDM5 inhibitor.
KDM5-C70 结构式
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 结构式
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 结构式
BCP25948 OG-L002 hydrochloride 1357298-75-9
OG-L002 HCl is an inhibitor of LSD1.
KDM4D-IN-1 结构式
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 结构式
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.
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