Home   >  
Epigenetics
  >  
Histone Methyltransferase

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

Histone Methyltransferase

Chemical Structure Cat. No. Product Name CAS No.
Valemetostat Chemical Structure
 BCP31915 Valemetostat 1809336-39-7
Valemetostat, also known as DS-3201, is an antineoplastic drug candidate.
A-893 Chemical Structure
 BCP31184 A-893 1868232-32-9
A-893 is a cell-active inhibitor of Methyltransferase SMYD2, with an IC50 of 2.8 nM.
3-Deazaneplanocin A hydrochloride Chemical Structure
 BCP21084 3-Deazaneplanocin A hydrochloride 120964-45-6
3-Deazaneplanocin A hydrochloride is a potent histone methyltransferase EZH2 inhibitor.
Sinefungin Chemical Structure
 BCP28648 Sinefungin 58944-73-3
Sinefungin is a potent inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viral multiplication. Sinefungin, a SET7/9 inhibitor, ameliorates renal fibrosis by inhibiting H3K4 methylation .
BCI-121 Chemical Structure
 BCP30688 BCI-121 432529-82-3
BCI-121 is an SMYD3 inhibitor. It acts by impairing cancer cell growth.
HLCL-61 Chemical Structure
 BCP24221 HLCL-61 586395-74-6
HLCL-61 is a potent and selective PRMT5 inhibitor for treatment of acute myeloid leukemia.
Chemical Structure
UNC669 Chemical Structure
 BCP27815 UNC669 1314241-44-5
UNC 669 is a potent antagonist of L3MBTL1(IC50=4.2 uM) and L3MBTL3(IC50=3.1 uM).
EPZ-020411 Chemical Structure
 BCP29978 EPZ-020411 1700663-41-7
EPZ020411 is a potent and selective inhibitor of PRMT6 with IC50 of 10 nM, has ＞10 fold selectivity for PRMT6 over PRMT1 and PRMT8.
EPZ020411 HCl Chemical Structure
 BCP29979 EPZ020411 HCl 2070015-25-5
EPZ020411 hydrochloride is a potent and selective inhibitor of PRMT6 with IC50 of 10 nM, has ＞10 fold selectivity for PRMT6 over PRMT1 and PRMT8.
123下一页末页共 66 条记录 1 / 7 页 
0086-15971444841