Z-FA-FMK ((1S)-Z-FA-FMK) is a potent Cathepsin B and L inhibitor. Z-FA-FMK blocks the induction of DEVDase activity, DNA fragmentation, and externalization of phosphatidylserine by selective synthetic retinoid-related molecules (RRMs). Z-FA-FMK inhibits apoptosis. Z-FA-FMK inhibits caspase activity and selectively inhibits recombinant effector caspases 2, -3, -6, and -7. Z-FA-FMK is a viral inhibitor. Z-FA-FMK inhibits reovirus replication in a susceptible host[1][2][3].
Molekulargewicht:
386.42
Reinheit:
99.14
CAS Nummer:
[197855-65-5]
Formel:
C21H23FN2O4
Target-Kategorie:
Apoptosis,Caspase,Cathepsin,SARS-CoV
Anwendungsbeschreibung:
MCE Product type: Reference compound
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