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Z-FA-FMK 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]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (1S)-Z-FA-FMK. CAS No. 197855-65-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P0109A. MedChemExpress MCE
Z-FA-FMK Z-FA-FMK is an irreversible cysteine protease inhibitor. It also inhibitits papain and cruzain. Group: Biochemicals. Grades: Highly Purified. CAS No. 197855-65-5. Pack Sizes: 1mg, 5mg. Molecular Formula: C21H23FN2O4, Molecular Weight: 386.42. US Biological Life Sciences. USBiological 1
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