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Chemical Structure : MU1656
Catalog No.: PC-38010Not For Human Use, Lab Use Only.
MU1656 (MU 1656 ) is a potent, highly selective inhibitor of histone methyltransferase DOT1L with IC50 of 2 nM.
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MU1656 (MU 1656 ) is a potent, highly selective inhibitor of histone methyltransferase DOT1L with IC50 of 2 nM.
MU1656 displays highly selectively against a panel of 37 methyltransferases.
MU1656 is more metabolically stable and significantly less toxic in vivo than pinometostat.
| M.Wt | 559.759 | |
| Formula | C32H45N7O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Khirsariya P, et al. J Med Chem. 2022 Apr 14;65(7):5701-5723.
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