MU1656 is a potent and selective inhibitor of histone methyltransferase DOT1L (IC50 = 2 nM), a key epigenetic regulatory protein involved in the development of cancers such as hematologic malignancies, thus MU1656 was able to significantly inhibit the proliferation of cancer cells and induce apoptosis.
Molecular Weight:
559.75
Purity:
96.92%
CAS Number:
[2766698-38-6]
Formula:
C32H45N7O2
Target:
Histone Methyltransferase
T63955
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