20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7378 | BRD9539 | Histone Methyltransferase | |
BRD9539 is an inhibitor of euchromatin histone methyltransferase 2 (EHMT2), also known as G9a, with an IC50 value of 6.3 μM | |||
T1923 | BRD4770 | Histone Methyltransferase | |
BRD4770 is a histone methyltransferase G9a inhibitor and induces cell senescence. | |||
T17204 | UNC0321 | Histone Methyltransferase | |
UNC0321 is an effective inhibitor of histone methyltransferase G9a with a Ki of 63 pM and with IC50s 9 nM and 6 nM in ECSD and CLOT assays. UNC0321 inhibits GLP with IC50s of 15 nM and 23 nM in ECSD and CLOT assays. | |||
T2354 | UNC 0631 | UNC0631 | Histone Methyltransferase |
UNC 0631 is a effectvie histone methyltransferase G9a inhibitor (IC50=4 nM). | |||
T17203 | UNC0224 | Histone Methyltransferase | |
UNC0224 is a selective inhibitor of G9a with a Ki of 2.6 nM and IC50 of 15 nM. UNC0224 also potently inhibits GLP with assay-dependent IC50 values of 20-58 nM. | |||
TQ0232 | UNC0646 | UNC 0646 | Histone Methyltransferase |
UNC0646 is a potent and selective inhibitor of the homologous protein lysine methyltransferases, G9a and GLP (IC50s: 6 nM/15 nM for G9a/GLP). UNC0646(UNC 0646) potently blocks G9a/GLP methyltransferase activity in cells ... | |||
T7194 | CM-272 | Apoptosis , DNA Methyltransferase , Histone Methyltransferase | |
CM-272 is a dual G9a/DNA methyltransferases (DNMTs) inhibitor. | |||
T4166 | UNC0642 | UNC-0642,UNC 0642 | Histone Methyltransferase |
UNC0642 is an effective and specific G9a/GLP inhibitor (IC50< 2.5 nM). | |||
T1959 | BIX-01294 trihydrochloride | BIX 01294 | Histone Methyltransferase , Autophagy |
BIX-01294 trihydrochloride is an inhibitor of G9a histone methyltransferase.In a cell-free assay, the IC50=2.7 μM for G9a histone methyltransferase. | |||
T7697 | BIX-01294 | Histone Methyltransferase , Autophagy | |
BIX-01294 is an G9a Histone Methyltransferase inhibitor(IC50 : 1.9 μM). | |||
T28112 | MS0124 | MS 0124,MS-0124 | Histone Methyltransferase |
MS0124 is a potent and selective G9A-like protein (GLP) inhibitor with IC50 values of 13±4 nM and 440±63 nM, respectively. | |||
T10882 | CPUY074020 | Histone Methyltransferase | |
CPUY074020 is a potent and orally bioavailable inhibitor of histone methyltransferase G9a (IC50: 2.18 μM) with anti-proliferative activity. | |||
T3624 | A-366 | A 366,A366 | Epigenetic Reader Domain , Histone Methyltransferase |
A-366 is a highly selective peptide-competitive histone methyltransferase G9a inhibitor with IC50s of 3.3 and 38 nM for G9a and GLP, respectively.It is more than 1,000-fold selective for G9a and GLP over the other 21 met... | |||
T10840L | CM-579 | DNA Methyltransferase , Histone Methyltransferase | |
CM-579 is a dual inhibitor of G9a and DNMT( IC50:16 nM, 32 nM for G9a and DNMT). It has potent in vitro cellular activity in a wide range of cancer cells. | |||
T3257 | UNC0638 | Influenza Virus , Histone Methyltransferase , Autophagy | |
UNC0638 is an inhibitor of β-protein lysine methyltransferases G9a(IC50<15 nM) and GLP(IC50=19 nM) with excellent potency and selectivity over a wide range of epigenetic and non-epigenetic targets. | |||
T63140 | LSD1-IN-20 | Histone Demethylase | |
Lsd1-in-20 is a potent dual inhibitor of LSD1/G9a with Ki values of 0.44 and 0.68 μM, respectively. LSD1-IN-20 showed antiproliferative activity against THP-1 leukemia cells and MDA-MB-231 breast cancer cells in vitro, w... | |||
T63351L | MS8511 HCl | MS8511 HCl(2866408-21-9 Free base) | Histone Methyltransferase |
MS8511 HCl is a selective and potent covalent inhibitor of G9a/GLP that acts by targeting cysteine residues in the substrate binding site. MS8511 has anticancer activity and antiproliferative activity and reduces intrace... | |||
T6803 | Chaetocin | Histone Methyltransferase , Antibacterial , Antibiotic | |
Chaetocin, a natural product from Chaetomium species, is a histone methyltransferase inhibitor with IC50 of 0.8 μM, 2.5 μM and 3 μM for dSU(VAR)3-9, mouse G9a and Neurospora crassa DIM5, respectively. | |||
T67947 | WDR5-0102 | Histone Methyltransferase | |
WDR5-0102 is a compound that inhibits the WDR5-MLL1 interface (K dis = 7 μM, K d = 4 μM), selectively reducing MLL1 HMT activity without affecting the human H3K4 methyltransferase SETD7 or other HMTs, including G9a, EHMT... | |||
T11185 | EML741 | Histone Methyltransferase | |
EML741 also inhibits DNMT1 (IC50, 3.1 μM), with no effect on DNMT3a or DNMT3b. EML741 exhibits low cell toxicity, and is membrane permeable and blood-brain barrier penetrated. EML741 is a histone lysine methyltransferase... |