| Cat. No. |
Product Name |
Information |
| PC-23669 |
ND-L11B
NSD2 degrader
|
ND-L11B is an effective degrader of RE-IIBP and NSD2-long, effectively induces NSD2 degradation with DC50 of 1.48 and 0.80 uM in KMS11 MM cell line, reduces H3K36me2 level in cancer cells. |
| PC-23666 |
Rabdosiin
METTL8 inhibitor
|
Rabdosiin is a tetramer of caffeic acid isolated from the stem of Ocimum sanctum, shows anti-allergic activity, anti-HIV activity and inhibition on DNA topoisomerase, also is a potential METTL8 inhibitor. |
| PC-23621 |
AS-254
ASH1L inhibitor
|
AS-254 is a highly potent and selective histone lysine methyltransferase ASH1L (absent, small, or homeotic-like 1) inhibitor with IC50 of 94 nM in FP assays, binds to the catalytic SET domain of ASH1L with ITC Kd of 179 nM. |
| PC-23618 |
AS-254s
ASH1L inhibitor
|
AS-254s is a highly potent and selective histone lysine methyltransferase ASH1L (absent, small, or homeotic-like 1) inhibitor with IC50 of 94 nM in FP assays, binds to the catalytic SET domain of ASH1L with ITC Kd of 179 nM. |
| PC-23492 |
ASH1L inhibitor AS-99 TFA
ASH1L inhibitor
|
ASH1L inhibitor AS-99 TFA (AS99) is a first-in-class, potent, selective inhibitor of ASH1L histone methyltransferase with IC50 of 0.79 uM. |
| PC-23491 |
ASH1L inhibitor AS-85 hydrochloride
ASH1L inhibitor
|
ASH1L inhibitor AS-85 hydrochloride (AS85) is a first-in-class, potent, selective inhibitor of ASH1L histone methyltransferase with IC50 of 0.6 uM. |
| PC-23490 |
ASH1L inhibitor AS-85
ASH1L inhibitor
|
ASH1L inhibitor AS-85 (AS85) is a first-in-class, potent, selective inhibitor of ASH1L histone methyltransferase with IC50 of 0.6 uM. |
| PC-23344 |
BR0063
PRC2 inhibitor
|
BR0063 is a potent, selective EED-directed allosteric inhibitor of polycomb repressive complex 2 (PRC2), efficiently blocks the interaction of the EED subunit with H3K27me3 (EC50=5.9 nM), which led to the marked inhibition of cellular PRC2 activity. |
| PC-23238 |
YD1342
PRMT4 inhibitor
|
YD1342 is the in-vivo active prodrug of YD1130, a potent, selective PRMT4 inhibitor with IC50 of <1 nM, 1000-fold selectivity for PRMT4 (IC50 < 0.5 nM). |
| PC-23237 |
YD1130
PRMT4 inhibitor
|
YD1130 is a potent, selective PRMT4 inhibitor with IC50 of <1 nM, 1000-fold selectivity for PRMT4 (IC50 < 0.5 nM) over a panel of 38 methyltransferases, including the other PRMTs. |
| PC-23204 |
SETD8 inhibitor C23
SETD8 inhibitor
|
SETD8 inhibitor C23 is a novel chemical inhibitor of SETD8, inhibits H4K20 methylation, inhibits IR-induced 53BP1 foci. |
| PC-23098 |
Igermetostat
EZH2 inhibitor
|
Igermetostat (XNW5004) is a potent, selective EZH2 inhibitor which potently inhibits both wild type and mutant EZH2. |
