About 6 results found for searched term "PRMTs" (0.125 seconds)
Cat.No. | Name | Target |
---|---|---|
M6177 | SGC2085 | PRMTs |
SGC2085 is a potent and selective Coactivator Associated Arginine Methyltransferase 1 (CARM1) inhibitor with an IC50 value of 50 nM and >100-fold selective over other PRMTs. | ||
M9003 | MS023 | PRMTs |
MS-023 | ||
MS023 is a potent and selective, cell-active inhibitor of type I PRMTs with IC50s of 4-119 nM. | ||
M10495 | AMI-1 disodium salt | PRMTs |
AMI1 | ||
AMI-1 is a potent and selective, cell-permeable and reversible inhibitor of protein arginine N-methyltransferases (PRMTs), with IC50 values of 8.8 μM and 3.0 μM for human PRMT1 and yeast-Hmt1p, respectively. AMI-1 is also a potent scavenger of NADPH-oxidase-derived superoxide. | ||
M10637 | GSK3368715 2HCl | PRMTs |
EPZ019997 2HCl | ||
GSK3368715 2HCl is a novel potent, orally active, reversible type I protein arginine methyltransferases (PRMTs) inhibitor, with IC50 values of 3.1 nM, 48 nM, 1148 nM, 5.7 nM and 1.7 nM for PRMT1, PRMT3, PRMT4, PRMT6, PRMT8, respectively. | ||
M13849 | MS023 dihydrochloride | PRMTs |
MS023 dihydrochloride is a potent, selective, and cell-active inhibitor of human type I protein arginine methyltransferases (PRMTs) inhibitor, with IC50s of 30, 119, 83, 4 and 5 nM for PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8, respectively. | ||
M28726 | GSK3368715 | Histone Methyltransferase |
EPZ019997 | ||
GSK3368715 (EPZ019997) is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (PRMTs) inhibitor (IC50=3.1 nM (PRMT1), 48 nM (PRMT3), 1148 nM (PRMT4), 5.7 nM (PRMT6), 1.7 nM (PRMT8)). GSK3368715 (EPZ019997) produces a shift in arginine methylation states, alters exon usage, and has strong anti-cancer activity. |
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