MJ-26 is an inhibitor targeting Menin. MJ-26 has high binding affinity (Ki: 0.56 µM) and significant antiproliferative activity. MJ-26 works by inhibiting Menin-MLL interaction and inducing Menin protein degradation. MJ-26 has significant antitumor effects on acute myeloid leukemia (AML). MJ-26 can be used in AML research[1].
Molekulargewicht:
757.97
Formel:
C38H47N9O4S2
Target-Kategorie:
Epigenetic Reader Domain
Anwendungsbeschreibung:
MCE Product type: Reference compound
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