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Cat. No. Product Name Information
PC-35295

CBB3001

LSD1 inhibitor

CBB3001 (CBB-3001) is a novel potent, selective histone demethylase LSD1 inhibitor with IC50 of 21.25 uM.
PC-43206

ORY-1001

LSD1 inhibitor

ORY-1001 (RG-6016) is a highly potent, selective inhibitor of lysine-specific demethylase KDM1A (LSD1) with IC50 of 18 nM, displays high selectivity for KDM1A over other FAD-containing monoamine oxidases.
PC-43163

ML324

KDM4 inhibitor

ML324 is a potent, selective JMJD2 demethylase (KDM4) inhibitor with IC50 of 920 nM for JMJD2E, shows no activity against LSD1 (>100-fold selectivity).
PC-43122

SP2509

LSD1 inhibitor

SP2509 is a potent, selective histone demethylase LSD1 (KDM1A) inhibitor with IC50 of 13 nM, shows no activity against MAOA, MAOB, LDH and glucose oxidase.
PC-42967

IOX1

2OG oxygenases inhibitor

IOX1 is a potent, broad-spectrum inhibitor of 2OG oxygenases, including the JmjC demethylases, with IC50 of <1 uM gainst the KDM3, KDM4 and KDM6, 5-25 uM against the KDM5 and KDM2/7.
PC-62978

L-α-Hydroxyglutaric acid disodium

Dioxygenase inhibitor

L-α-Hydroxyglutaric acid disodium (L-2-Hydroxyglutarate, L-2-HG) competitive inhibitor of multiple α-KG-dependent dioxygenases, including histone demethylases and the TET family of 5-methlycytosine (5mC) hydroxylases.
PC-62871

Bizine

LSD1 inhibitor

Bizine is a phenelzine analog that inhibits LSD1 with Ki of 59 nM, displays 23-fold, 63-fold, and >100-fold selectivity for LSD-1 over MAOA, MAOB, and LSD2 respectively.
PC-62840

LSD1-IN-11p

LSD1 inhibitor

LSD1-IN-11p is a potent, reversible LSD1 inhibitor with IC50/Kd of 79/21 nM.
PC-62837

KDM4D-IN-10r

KDM4D inhibitor

KDM4D-IN-10r is a potent, selective histone lysine demethylase 4D (KDM4D) inhibitor with IC50 of 0.41 uM.
PC-62835

KDM5A-IN-50

KDM5 inhibitor

KDM5A-IN-50 is a potent, selective, and orally bioavailable pan KDM5 enzyme inhibitor with biochemical IC50 of 45/56/55 nM for KDM5A/KDM5B/KDM5C respectively.
PC-62327

AS8351

KDM5B inhibitor

AS8351 (NS 51355) is a small molecule that induces reprogramming of human fetal lung fibroblasts into functional cardiomyocytes, in combination with CHIR 99021, A83-01, BIX 01294, SC1, Y-27632, OAC2, SU 16f and JNJ 10198409, inhibits lysine demethylase 5B (KDM5B).
PC-62294

KDM5-C49

KDM5 inhibitor

KDM5-C49 is a potent, selective KDM5 inhibitor with IC50 of 25, 30 and 59 nM for KDM5A, B and C, respectively.

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