| Cat. No. |
Product Name |
Information |
| PC-22923 |
MS3745
G9a-like protein inhibitor
|
MS3745 is a potent and selective inhibitor of protein lysine methyltransferase G9a-like protein (GLP) with IC50 of 4 nM, 65-fold selective over G9a. |
| PC-22922 |
MS3748
G9a-like protein inhibitor
|
MS3748 is a potent and selective inhibitor of protein lysine methyltransferase G9a-like protein (GLP) with IC50 of 5 nM, 59-fold selective over G9a. |
| PC-22921 |
EML741
G9a/GLP inhibitor
|
EML741 is a potent, selective inhibitor of H3K9-specific methyltransferases G9a/G9a-like protein (G9a/GLP) with IC50 of 23 nM (G9a), KD of 1.13 uM in MST assays. |
| PC-22846 |
CDYL inhibitor Compound D03
CDYL inhibitor
|
Compound D03 is a potent and selective small-molecule inhibitor of histone methyllysine reader protein chromodomain Y-like (CDYL) with SPR KD of 0.5 uM, disrupts the recruitment of CDYL onto chromatin. |
| PC-22809 |
AM-9747
PRMT5 inhibitor
|
AM-9747 (AM9747) is a potent, selective and MTA cooperative PRMT5 inhibitor, inhibits symmetrical dimethyl arginine methylation (SDMA) levels in HCT116 MTAP-deleted cells with IC50 of 2 nM. |
| PC-22808 |
AZ-PRMT5i-1
PRMT5 inhibitor
|
AZ-PRMT5i-1 is a potent, selective and MTA-cooperative PRMT5 inhibitor with IC50 of 5.5 nM in symmetrical dimethyl arginine methylation (SDMA) cellular imaging assay. |
| PC-22701 |
G9a/NSD2 dual inhibitor 16
G9a/NSD2 inhibitor
|
G9a/NSD2 dual inhibitor 16 (W4032) is a highly potent G9a/NSD2 dual inhibitor with IC50 of 241/17 nM respectively, shows potent cell growth inhibition against PANC-1 and MDA-MB-231 with IC50 values of 0.44 and 0.72 μM, respectively. |
| PC-22471 |
DC-Y13-27
YTHDF2 inhibitor
|
DC-Y13-27 is a specific inhibitor of N6-methyladenosine (m6A) reader YTHDF2, inhibits YTHDF2 binding to m6A-containing RNA with IC50 of 21.8 uM, directly binds to YTHDF2 with a binding constant (KD) of 37.9 uM in MST assay. |
| PC-22428 |
YTHDC1 inhibitor 40
YTHDC1 inhibitor
|
YTHDC1 inhibitor 40 is a potent, selective m6A reader YTHDC1 inhibitor with ITC Kd of 49 nM, HTRF IC50 of 0.35 uM. |
| PC-22354 |
PRMT9 inhibitor LD2
PRMT9 inhibitor
|
PRMT9 inhibitor LD2 is a specific small molecule PRMT9 inhibitor, inhibits PABPC1 R493 methylation level with IC50 of 0.9 uM in in Molm13s, sparing other PRMTs. |
| PC-22335 |
iCARM1
CARM1 inhibitor
|
iCARM1 (ZINC65534584) is a potent, selective inhibitor of protein arginine methyltransferase CARM1 (PRMT4) with IC50 of 12.3 uM, Biacore Kd of 0.67 uM. |
| PC-22311 |
WDR5 WIN site inhibitor C6 TFA
WDR5 inhibitor
|
WDR5 inhibitor C6 TFA is a highly potent WDR5 WIN site inhibitor with Kd of 0.1 nM.
|
