Z-FF-FMK is a selective cathepsin-L inhibitor. Z-FF-FMK can prevent beta-amyloid to induce apoptotic changes such as activation of caspase-3, cleavage of the DNA repair enzyme, poly-ADP ribose polymerase, and DNA fragmentation[1].
Molecular Weight:
462.51
Purity:
98.71
CAS Number:
[105608-85-3]
Formula:
C27H27FN2O4
Target:
Cathepsin
Application Notes:
Peptides
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