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Histone Methyltransferase

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Histone Methyltransferase

Chemical Structure Cat. No. Product Name CAS No.
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.
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.
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