MU1656 是一种有效和选择性的组蛋白甲基转移酶DOT1L抑制剂，IC50值为 2 nM。MU1656 可用于血液系统恶性肿瘤的研究。
| 生物活性 | MU1656 is a potent and selective inhibitor ofhistone methyltransferaseDOT1L, with anIC50of 2 nM. MU1656 can be used for the research of hematological malignancies[1]. |
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| 运输条件 | Room temperature in continental US; may vary elsewhere. |
| 储存方式 | Please store the product under the recommended conditions in the Certificate of Analysis. |
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