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Cat. No. Product Name Information
PC-24016

EP652

METTL3 inhibitor

EP652 is a potent, selective and in vivo active inhibitor of RNA methyltransferase METTL3 with IC50 of 2 nM (METTL3/14) in SPA primary assays.
PC-23957

DDD1870799

RNMT inhibitor

DDD1870799 is a small molecule inhibitor o fHsRNMT (RNA guanine-7 methyltransferase)-RAM (RNA guanine-N7 methyltransferase activating subunit) complex, binds competitively with cap and binds effectively to HsRNMT-RAM in the presence of the co-product SAM wth Kd of 2.5 uM.
PC-23956

DDD1060606

RNMT inhibitor

DDD1060606 is a small molecule inhibitor o fHsRNMT (RNA guanine-7 methyltransferase)-RAM (RNA guanine-N7 methyltransferase activating subunit) complex, binds competitively with cap and binds effectively to HsRNMT-RAM in the presence of the co-product SAM wth Kd of 1.6 uM.
PC-23905

CSV0C018875

G9a inhibitor

CSV0C018875 is a cell active quinoline based G9a inhibitor with IC50 of 67.02 uM.
PC-23904

HKMTI-1-248

G9a/GLP inhibitor

HKMTI-1-248 is a potent and selective G9a/GLP inhibitor with IC50 of 13 nM (G9a), equipotent against G9a and GLP (G9a-like protein, EHMT1).
PC-23903

EPZ035544

G9a/GLP inhibitor

EPZ035544 is a potent inhibitor of histone methyltransferase G9a/GLP with IC50 of 10 nM/<100 nM respectively.
PC-23902

ZZM-1220

G9a/GLP inhibitor

ZZM-1220 is a potent, selective G9a/GLP covalent inhibitor with IC50 of 458/924 nM respectively.
PC-23669

ND-L11B

NSD2 degrader

ND-L11B is an effective degrader of RE-IIBP and NSD2-long, effectively induces NSD2 degradation with DC50 of 1.48 and 0.80 uM in KMS11 MM cell line, reduces H3K36me2 level in cancer cells.
PC-23666

Rabdosiin

METTL8 inhibitor

Rabdosiin is a tetramer of caffeic acid isolated from the stem of Ocimum sanctum, shows anti-allergic activity, anti-HIV activity and inhibition on DNA topoisomerase, also is a potential METTL8 inhibitor.
PC-23621

AS-254

ASH1L inhibitor

AS-254 is a highly potent and selective histone lysine methyltransferase ASH1L (absent, small, or homeotic-like 1) inhibitor with IC50 of 94 nM in FP assays, binds to the catalytic SET domain of ASH1L with ITC Kd of 179 nM.
PC-23618

AS-254s

ASH1L inhibitor

AS-254s is a highly potent and selective histone lysine methyltransferase ASH1L (absent, small, or homeotic-like 1) inhibitor with IC50 of 94 nM in FP assays, binds to the catalytic SET domain of ASH1L with ITC Kd of 179 nM.
PC-23492

ASH1L inhibitor AS-99 TFA

ASH1L inhibitor

ASH1L inhibitor AS-99 TFA (AS99) is a first-in-class, potent, selective inhibitor of ASH1L histone methyltransferase with IC50 of 0.79 uM.

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