Irreversible inhibitor of cathepsin L.
Product Details
| Alternative Name: | Z-FY(tBu)-DMK |
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| Formula: | C31H34N4O5 |
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| MW: | 542.6 |
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| Purity: | ≥98% |
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| Appearance: | White to off-white powder. |
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| Solubility: | Soluble in ethyl acetate (10mg/ml) or DMSO. |
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| Shipping: | Ambient |
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| Long Term Storage: | -20°C |
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| Handling: | Protect from light. |
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| Regulatory Status: | RUO - Research Use Only |
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Product Literature References
Identification of host factors involved in borna disease virus cell entry through a small interfering RNA functional genetic screen: R. Clemente, et al.; J. Virol.
84, 3562 (2010),
Abstract;
Full Text
Analysis of filovirus entry into vero e6 cells, using inhibitors of endocytosis, endosomal acidification, structural integrity, and cathepsin (B and L) activity: A. Sanchez; J. Infect. Dis.
196, S251 (2007),
Abstract;
Full Text
Loss of cathepsin L activity promotes claudin-1 overexpression and intestinal neoplasia: F. Boudreau, et al.; FASEB J.
21, 3853 (2007),
Abstract;
Full Text
The affinity-labelling of cathepsin S with peptidyl diazomethyl ketones. Comparison with the inhibition of cathepsin L and calpain: E. Shaw, et al.; FEBS Lett.
334, 340 (1993),
Abstract;
