PK68 is a potent orally active and specifical type II inhibitor of receptor-interacting kinase 1 (RIPK1) with an IC50 of ~90 nM, displays inhibition of RIPK1-dependent necroptosis. PK68 powerfully ameliorates TNF-induced systemic inflammatory response syndrome, and can be used for the research of inflammatory disorders and cancer metastasis[1].
Molekulargewicht:
424.52
Reinheit:
99.92
CAS Nummer:
[2173556-69-7]
Formel:
C22H24N4O3S
Target-Kategorie:
RIP kinase
Anwendungsbeschreibung:
MCE Product type: Reference compound
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