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首页-小分子抑制剂&激动剂-Epigenetics-Histone Methyltransferase (HMTase)

Request The Product List ofHistone Methyltransferase (HMTase) Histone Methyltransferase (HMTase)

Cat. No. Product Name Information
PC-42405

GSK3326595

PRMT5 inhibitor

Pemrametostat (GSK3326595, EPZ015938) is a potent, selective, reversible and orally active PRMT5 inhibitor with IC50 of 22 nM.
PC-42321

EED226

PRC2 inhibitor

EED226 (EED 226) is a potent, selective, orally bioavailable PRC2 inhibitor that directly binds to the H3K27me3 binding pocket of EED (IC50=22 nM).
PC-45115

EPZ-011989 trifluoroacetate

EZH2 inhibitor

EPZ-011989 trifluoroacetate is a potent, selective, orally bioavailable inhibitor of EZH2 with Ki of < 3 nM.
PC-45114

EPZ-011989

EZH2 inhibitor

EPZ-011989 (EPZ011989) is a potent, selective, orally bioavailable inhibitor of EZH2 with Ki of < 3 nM.
PC-42113

MS049

PRMT4/6 inhibitor

MS049 is a potent, selective, and cell-active dual inhibitor of PRMT4 and PRMT6 with IC50 of 34±10 nM and 43±7 nM, respectively.
PC-42097

EPZ-015866

PRMT5 inhibitor

EPZ-015866 (GSK-591, GSK-3203591) is a potent, selective protein methyltransferase 5 (PRMT5) inhibitor with IC50 of 4 nM.
PC-42198

SGC2085

CARM1 inhibitor

SGC2085 is a potent, selective protein arginine methyltransferase PRMT4 (CARM1) inhibitor with IC50 of 50 nM, displays >100-fold selectivity over other PRMTs (PRMT6 IC50=5.3 uM).
PC-42272

UNC3866

CBX7 inhibitor

UNC3866 is a potent, selective PRC1 chromodomains antagonist that binds to CBX4 and CBX7 with Kd of 100 nM.
PC-42740

UNC0224

G9a/GLP inhibitor

UNC0224 (UNC-0224) is a potent, selective G9a/GLP inhibitor with IC50 of 57 nM and 58 nM in biochemical assays.
PC-42081

A-196

SUV420H1 inhibitor

A-196 is a potent, selective and substrate-competitive inhibitor of protein lysine methyltransferases (PKMTs) SUV420H1 and SUV420H2 with IC50 of 25 nM and 144 nM, respectively.
PC-45598

LLY-507

SMYD2 inhibitor

LLY-507 is a potent, selective and cell-active inhibitor of SMYD2 (IC50<15 nM).
PC-45617

WDR5-0103

MLL1-WDR5 inhibitor

A potent MLL1-WDR5 interaction inhibitor with IC50 of 26.4 nM in competitive binding assay.

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