Cell permeable, potent and selective proteasome inhibitor originally isolated from Actinomycetes strain based on its potent in vivo antitumor activity. More potent inhibitor of the chymotrypsin-like activity of the proteasome than lactacystin (Prod. No.
Molekulargewicht:
554.7
Reinheit:
95% (HPLC)
Sequenz:
D-Phe-Pro-Arg-chloromethylketone
CAS Nummer:
[134381-21-8]
Formel:
C28H50N4O7
Target-Kategorie:
Proteasome
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