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Cat. No. Product Name Information
PC-26996

TNG917

EHMT1/2 inhibitor

TNG917 is a potent, selective, histone substrate-competitive, orally active dual inhibitor of EHMT1/2, shows high selectivity over other methyltransferases.
PC-26788

AZD3470

PRMT5 inhibitor

AZD3470 (AZD-3470) is a potent, seleective MTA-cooperative PRMT5 inhibitor, targets MTAP deficient advanced/metastatic cancer cells.
PC-26787

TNG456

PRMT5 inhibitor

TNG456 is a potent, highly selective, brain-penetrant MTA-cooperative PRMT5 inhibitor with Ki,app of <2 pM, exhibits viability growth inhibition with GI50 of 20 nM for HAP1 MTAP-null cells, 50-fold selective over HAP1 MTAP WT cells.
PC-26595

SCR-6920

PRMT5 inhibitor

SCR-6920 is a potent and selective, oral PRMT5 inhibitor with IC50 of 1.48 nM.
PC-26591

NSUN2 inhibitor AK

NSUN2 inhibitor

NSUN2 inhibitor AK (AK-968/36977265) is a small molecule inhibitor of RNA methyltransferase NSUN2, decreases m5C occupancy and GATM mRNA levels, shows anti-fibrotic efficacy.
PC-26589

UNC7242

PHF1/PHF19 inhibitor

UNC7242 is a small molecule antagonist of PRC2 components PHF1 and PHF19 with ITC Kd of 1.13 uM and 0.64 uM, displaces recombinant or endogenous PHF1 or 19 from nucleosomes.
PC-26542

EP102

METTL3 inhibitor

EP102 is a potent, selective METTL3 inhibitor with IC50 of 2 nM in SPA primary assay.
PC-26532

METTL16-IN-1

METTL16 inhibitor

METTL16-IN-1 is a specific small molecule METTL16 inhibitor with IC50 of 1.7 uM against the METTL16-RNA binding.
PC-26496

C191-0266

METTL3 inhibitor

C191-0266 is a small molecule inhibitor of METTL3 with KD of 7.28 uM and enzymatic IC50 of 7.84 uM.
PC-26384

METTL9i

METTL9 inhibitor

METTL9i is a first-in-class, highly potent, selective and cell-active methyltransferase METTL9 inhibitor with IC50 of 67 nM.
PC-26274

SGSS05NS

SETD8 inhibitor

SGSS05NS is a potent, selective and covalent inhibitor of protein lysine methyltransferase (PKMT) SETD8 with IC50 of 0.54 uM, covalently modifies SETD8 at Cys311.
PC-26273

MS4138

SETD8 inhibitor

MS4138 is a potent, selective and covalent inhibitor of protein lysine methyltransferase (PKMT) SETD8 with IC50 of 1.4 uM, covalently modifies SETD8 at Cys311.

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