| Cat. No. |
Product Name |
Information |
| PC-23356 |
S2157
LSD1 inhibitor
|
S2157 is a selective, brain-permeable inhibitor of lysine-specific demethylase 1 (LSD1, KDM1A) with IC50 of 0.89 uM, >200-fold selective over LSD2, MAO-A and MAO-B. |
| PC-23355 |
S2172
LSD1 inhibitor
|
S2172 is a specific, brain penetrant inhibitor of lysine-specific demethylase 1 (LSD1, KDM1A) with Ki of 0.27 uM. |
| PC-23354 |
S2116
LSD1 inhibitor
|
S2116 is a specific, brain penetrant inhibitor of lysine-specific demethylase 1 (LSD1, KDM1A) withIC50 of 0.74 uM. |
| PC-23285 |
NCL-1
LSD1 inhibitor
|
NCL-1 is a specific small molecule inhibitor of LSD1 (KDM1A) with IC50 of 2.5 uM. |
| PC-23163 |
P3FI-63
KDM3B inhibitor
|
P3FI-63 is a small molecule PAX3-FOXO1 activity inhibitor, blocks PAX3-FOXO1 downstream target gene expression, inhibits multiple KDMs including KDM3B, KDM4B, KDM5A, and KDM6B, with highest potency against KDM3B (IC50=7 uM). |
| PC-22985 |
YTH domain inhibitor N-7
m6A YTH domain inhibitor
|
YTH domain inhibitor N-7 is a specific small molecule, pan-inhibitor of YTH domain-containing m6A RNA readers with IC50 of 30-48 uM for human YTHDF1, YTHDF2, YTHDF3, YTHDC1, and YTHDC2 proteins. |
| PC-22960 |
ML234
EZH2/LSD1 inhibitor
|
ML234 is a potent EZH2/LSD1 dual inhibitor with IC50 of 0.09/0.12 uM respectively, shows excellent antiproliferative capacity against prostate cancer cell lines LNCAP, PC3, and 22RV1. |
| PC-22951 |
GSK-J5
|
GSK-J5 is the ethyl ester pro-drug of GSK-J2, which lacks H3K27 demethylase activity as a inactive control molecule for GSK-J4. |
| PC-22847 |
FTO inhibitor FB23
FTO inhibitor
|
FTO inhibitor FB23 is a potent and selective FTO demethylase inhibitor with IC50 of 60 nM, directly binds to FTO and selectively inhibits FTO's mRNA N6-methyladenosine (m6A) demethylase activity. |
| PC-22677 |
DDO-2728
ALKBH5 inhibitor
|
DDO-2728 is a selectiv, 2-OG independent inhibitor of mRNA m6A demethylase AlkB homologue 5 (ALKBH5) with IC50 of 2.97 uM in FP assays, does not inhibit FTO (ALKBH9) and ALKBH3. |
| PC-22581 |
TACH101 L-lysine
KDM4 inhibitor
|
TACH101 (Zavondemstat, QC8222, TACH 101) L-lysine is a reversible, α-ketoglutarate competitive, selective and potent inhibitor of KDM4 isoforms A-D with IC50 values of 80 nM against all four isoforms. |
| PC-22360 |
KDM4/5 inhibitor 19a
KDM4/5 inhibitor
|
KDM4/5 inhibitor 19a is a potent, cell penetrant, dual KDM4/5-subfamily inhibitor with Ki values of 4 nM/7 nM for KDM4A/KDM5B, respectively. |
