Epigenetics
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 24017 | AMG-193 | 2790567-82-5 | 98.62%; EE 98.28% |  |
| AMG-193 is an oral, small-molecule, methylthioadenosine-cooperative inhibitor of the | ||||
| 20471 | FHD-286 | 2671128-05-3 | ≧98.0% |  |
| FHD-286 is an oral, small-molecule, selective, allosteric inhibitor of BRG1 and BRM i | ||||
| 20549 | STC-15 | 2648257-56-9 | ≧98.0% |  |
| STC-15 is a first-in-class inhibitor of RNA modification and is the first ever RNA me | ||||
| 20646 | TNG908 | 2760481-53-4 | ≧98.0% |  |
| TNG908 is a clinical stage MTA-cooperative PRMT5 inhibitor that is selectively active | ||||
| 20610 | Zavondemstat | 1851412-93-5 | ≧98.0% |  |
| Zavondemstat is a KDM4 inhibitor with potential as an antineoplastic agent. | ||||
| 16122736 | Lirametostat ( CPI-1205 ) | 1621862-70-1 | ≧98.0% | _1621862-70-1.png) |
| Lirametostat ( CPI-1205 ) is a potent, selective, and cofactor-competitive inhibitor | ||||
| 24001 | Bomedemstat | 1990504-34-1 | ≧98.0% |  |
| Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl | ||||
| 2073104 | Enarodustat ( JTZ-951 ) | 1262132-81-9 | 98% Min. | _1262132-81-9.png) |
| Enarodustat ( JTZ-951 ) is an orally-active HIF-PH inhibitor with an EC50 of 0.22 Μm | ||||
| 52001 | Selisistat ( EX-527 ) | 49843-98-3 | ≧98.0% |  |
| Selisistatwas the first identified potent and cell permeable SIRT1-specific inhibitor | ||||
| 24008 | RNK-05047 | 2503036-46-0 | ≧98.0% |  |
| RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi | ||||
| 24013 | Ziftomenib ( KO-539 ) | 2134675-36-6 | ≧98.0% | _2134675-36-6.png) |
| Ziftomenib is an oral, potent, and selective small molecule inhibitor that targets th | ||||
| 24018 | AM-9747 | 2691869-82-4 | ≧98.0% |  |
| AM-9747 is an MTA cooperative PRMT5 inhibitor. AM-9747 selectively inhibited the prol | ||||