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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-70104

MM-589

MLL1/WDR5 inhibitor

MM-589 is a highly potent, cell-permeable inhibitor of WDR5-MLL interaction with IC50 of 0.9 nM, Ki of <1 nM.
PC-60300

MS-453

SETD8 inhibitor

MS-453 (MS453) is a potent, selective and covalent protein lysine methyltransferase SETD8 inhibitor with IC50 of 804 nM.
PC-60299

CPI-1205

Lirametostat (CPI-1205) is a highly potent, selective EZH2 inhibitor with biochemical IC50 of 2 nM, cellular EC50 of 32 nM.
PC-60263

JQEZ5

EZH2 inhibitor

JQEZ5 (JQ5, EZ005) is a novel potent, selective, SAM-competitive EZH2 inhibitor with IC50 of 80 nM (inhibition of enzymatic function of PRC2).
PC-60256

CM-579

G9a inhibitor

CM-579 (CM579) is a novel potent, selective and reversible dual inhibitor of G9a/DNMTs with IC50 of 16 nM and 32 nM for G9a and DNMT1, respectively.
PC-60255

CM-272

G9a/DNMTs inhibitor

CM-272 (CM272) is a novel potent, selective and reversible dual inhibitor of G9a/DNMTs with IC50 of 8 nM and 382 nM for G9a and DNMT1, respectively.
PC-70002

MIV-6R

menin-MLL inhibitor

MIV-6R is a potent, ligand-efficient, and cell-active inhibitor menin-MLL interaction with IC50 of 56 nM, Kd of 85 nM.
PC-60001

PF-06821497 S enantiomer

PF-06821497 S enantiomer is a novel potent, selective, orally bioavailable EZH2 inhibitor with Ki of <0.1 and 1.15 nM aginast both wt and mutant Y641N EZH2, respectively.
PC-45679

XY1

XY1 is the inactive control compound of SGC-707, shows no inhibition on PRMT3.
PC-45465

UNC1079

UNC1079 is the piperidine analog of UNC1021, structurally similar but significantly less potent inhibitor for use as a negative control in cellular studies (L3MBTL3 of >10 uM by AlphaScreen, >1000-fold weaker than UNC1215).
PC-45680

SGC707

PRMT3 inhibitor

SGC707 (SGC 707) is a potent, selective and cell-active allosteric inhibitor of PRMT3 (IC50=31 nM, Kd=53 nM).
PC-45658

MS023

PRMT1 inhibitor

MS023 is a potent, selective, and cell-active inhibitor of type I PRMTs with IC50s of 30/119/83/4/5 nM for PRMT1/3/4/6/8 respectively.

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