| Cat. No. |
Product Name |
Information |
| PC-21085 |
JMJD5 inhibitor 19j
JMJD5 inhibitor
|
JMJD5 inhibitor 19j is a potent selective small molecule inhibitor of 2OG-dependent oxygenase JMJD5 (KDM8), shows high selectivity over other human 2OG oxygenases. |
| PC-20876 |
ZY0511
LSD1 inhibitor
|
ZY0511 is a highly selective and potent inhibitor of lysine‐specific histone demethylase 1 (LSD1) with IC50 of 1.7 nM and SPR Kd of 2.42 nM. |
| PC-20519 |
TAK-418
LSD1 (KDM1A) inhibitor
|
TAK-418 (TAK418) is a potent, specific inhibitor of LSD1 (KDM1A) enzyme activity with IC50 of 2.9 nM. |
| PC-20355 |
KDM5B inhibitor 27ab
KDM5B inhibitor
|
KDM5B inhibitor 27ab is a potent inhibitor of histone lysine specific demethylase 5B (KDM5B/JARID1B) with IC50 of 24.4 nM. |
| PC-20354 |
KDM5A inhibitor compound 1
KDM5A inhibitor
|
KDM5A inhibitor compound 1 (ZINC33576) is a potent, selective KDM5A (JARID1A) inhibitor with IC50 of 23.8 nM. |
| PC-20352 |
EPZ020809
KDM4C inhibitor
|
EPZ020809 is a potent, specific KDM4C inhibitor with Ki of 31 nM, binds KDM4C in a 2-OG-competitive fashion. |
| PC-49236 |
FTO-43
FTO inhibitor
|
FTO-43 (FTO-43 N) is a potent, selective inhibitor of the m6A demethylase fat mass- and obesity-associated protein (FTO) with IC50 of 1.0 uM, no significant acitivity against the homologous m6A RNA demethylase ALKBH5 (IC50>40 uM). |
| PC-38672 |
Pulrodemstat besylate salt
LSD1 inhibitor
|
Pulrodemstat (CC-90011) is a potent, selective, reversible and orally active inhibitor of lysine specific demethylase-1 (LSD1) with biochemical IC50 of 0.3 nM. |
| PC-38671 |
Pulrodemstat
LSD1 inhibitor
|
Pulrodemstat (CC-90011) is a potent, selective, reversible and orally active inhibitor of lysine specific demethylase-1 (LSD1) with biochemical IC50 of 0.3 nM. |
| PC-38508 |
GSK-J1
KDM6A/6B inhibitor
|
GSK-J1 is a potent, selective inhibitor of the H3K27 histone demethylases JMJD3 (KDM6B) and UTX (KDM6A) with IC50 of 28 nM and 53 nM, respectively. |
| PC-72264 |
JMJD7 inhibitor compound 3 (Cpd-3)
JMJD7 inhibitor
|
JMJD7 inhibitor compound 3 (Cpd-3) is the first small molecule inhibitor of JMJD7 with IC50 of 6.62 uM, efficiently bind to JMJD7 in vitro, displays good inhibitory activity against cancer cell lines expressing a high level of JMJD7. |
| PC-72263 |
MINA53 inhibitor 10
MINA53 inhibitor
|
MINA53 inhibitor 10 is a first in class, potent, selective MINA53 inhibitor with IC50 of 1.5 uM, selective over NO66, KDM4-6 and other JmjC oxygenases. |
