XRK3F2 is a p62 (sequestosome-1) ZZ domain inhibitor that has specificity for the p62-ZZ domain over other p62 signaling domains. XRK3F2 blocks TNFalpha effects and upregulation in bone marrow stromal cells, and induces multiple myeloma cell apoptosis. XRK3F2 can be used for the research of multiple myeloma bone disease, acute myeloid leukemia, and multiple myeloma[1][2][3].
Molekulargewicht:
435.89
Reinheit:
99.08
CAS Nummer:
[2375193-43-2]
Formel:
C23H24ClF2NO3
Target-Kategorie:
Autophagy,p62
Anwendungsbeschreibung:
MCE Product type: Reference compound
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