Z-FA-FMK

Z-FA-FMK

Z-FA-FMK

Chemical compound


Z-FA-FMK, abbreviating for benzyloxycarbonyl-phenylalanyl-alanyl-fluoromethyl ketone, is a very potent irreversible inhibitor of cysteine proteases, including cathepsins B, L, and S, cruzain, and papain. It also selectively inhibits effector caspases 2, 3, 6, and 7 but not caspases 8 and 10.[1] This compound has been shown to block the production of IL1-α, IL1-β, and TNF-α induced by LPS in macrophages by inhibiting NF-κB pathways.

Quick Facts Names, Identifiers ...

References

  1. Lawrence CP, et al. (15 September 2006). "The cathepsin B inhibitor, Z-FA-FMK, inhibits human T cell proliferation in vitro and modulates host response to pneumococcal infection in vivo". Journal of Immunology. 177 (6): 3827–36. doi:10.4049/jimmunol.177.6.3827. PMID 16951345. S2CID 23419301.



Share this article:

This article uses material from the Wikipedia article Z-FA-FMK, and is written by contributors. Text is available under a CC BY-SA 4.0 International License; additional terms may apply. Images, videos and audio are available under their respective licenses.