Name | BBDDL2059 |
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Description | BBDDL2059 is a selective covalent inhibitor of histone methyltransferase EZH2 with an IC50 of 1.5 nM for EZH2-Y641F. BBDDL2059 inhibits lymphoma cell growth at nanomolar concentrations and can be used for anticancer research[1]. |
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Related Catalog | |
Target |
EZH2 Y641F mutant type:1.5 nM (IC50) |
References |
Molecular Formula | C27H36N4O4S |
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Molecular Weight | 512.66 |