MU1656 is Highly Selective Inhibitor of Methyltransferase DOT1L (IC50 = 2 nM), and carbocyclic C-nucleoside analogues of the natural nucleoside derivative EPZ004777. MU1656 can potently and selectively inhibit DOT1L in vitro as well as in the cell.
MedKoo Cat#: 466018
Name: MU1656
CAS#: unknown
Chemical Formula: C32H45N7O2
Exact Mass: 559.3635
Molecular Weight: 559.76
Elemental Analysis: C, 68.66; H, 8.10; N, 17.52; O, 5.72
The following data is based on the product molecular weight 559.76 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
| 5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
| 10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
| 50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
