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Tocris™ SGC 0946
Highly potent and selective DOT1L inhibitor; cell permeable
Supplier: Tocris™ 4541/2
Description
SGC 0946 is a highly potent DOT1L methyltransferase inhibitor (Kd = 0.06 nM, IC50 = 0.3 nM in a radioactive assay); blocks H3K79 methylation in A431 cells and MCF10A cells. Inactive at 12 histone methyltransferases and DNMT1. Selectively kills cells transformed with the MLL-AF9 fusion oncogene in an in vitro model of leukemia; lowers levels of MLL target genes HOXA9 and Meis1.To request the negative control for SGC0946, please fill out the SGC0649 request form on the SGC website.
Specifications
1-[3-[[[(2 R,3 S,4 R,5 R)-5-(4-Amino-5-bromo-7 H-pyrrolo[2,3-d]pyrimidin-7-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl](isopropyl)amino]propyl]-3-[4-(2,2-dimethylethyl)phenyl]urea | |
2 mg | |
C28H40BrN7O4 |
1561178-17-3 | |
Lysine Methyltransferase Inhibitors | |
99% |
Safety and Handling
Recommended Storage : Store at -20°C
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