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.
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.
SGC2085 Chemical Structure
BCP25834 SGC2085 1821908-48-8
SGC2085 is a potent and selective coactivator associated arginine methyltransferase 1 (CARM1) inhibitor with an IC50 of 50 nM.
AZ505 ditrifluoroacetate Chemical Structure
BCP29703 AZ505 ditrifluoroacetate 1035227-44-1
AZ505 ditrifluoroacetate is a potent and selective SMYD2 inhibitor with IC50 of 0.12 μM.
AZ-505 Chemical Structure
BCP20970 AZ-505 1035227-43-0
AZ505 is a potent and selective SMYD2 inhibitor with IC50 of 0.12 μM.
123下一页末页共 63 条记录 1 / 7 页 
0086-13720134139