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A synthetic peptide inhibitor that inhibits caspase-13 and related caspase activity. FMK inhibitors are irreversible and non-toxic, and can be used in both in vivo and in vitro studies.
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M.F/Formula | C32H45FN4O12 |
M.W/Mr. | 696.7 |
Sequence | LEED (Modifications: N-terminal benzyloxycarbonyl; C-terminal FMK; Glu-2 = Glu(OMe); Glu-3 = Glu(OMe); Asp-4 = Asp(OMe)) |
Labeling Target | Caspase 13 |
Purity | >95% |
Activity | Inhibitor |
Source# | Synthetic |
Long-term Storage Conditions | Soluble in DMSO |
1. Cationic cell-penetrating peptides are potent furin inhibitors
2. Myotropic activity of allatostatins in tenebrionid beetles
3. Autoinhibition and phosphorylation-induced activation of phospholipase C-γ isozymes
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