Inhibitor SourceBook™ Second Edition
Inhibitor SourceBook™ Second Edition
Inhibitor SourceBook™ Second Edition
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Proteases<br />
Anthrax Lethal Factor (LF) Metalloprotease <strong>Inhibitor</strong>s<br />
Calbiochem • <strong>Inhibitor</strong> SourceBook<br />
Proteases<br />
Product Cat. No. Comments Size Price<br />
Anthrax Lethal Factor Protease 176901 [Anthrax LF Protease <strong>Inhibitor</strong>; Bacillus anthracis LF Protease <strong>Inhibitor</strong>;<br />
mg $ 95<br />
<strong>Inhibitor</strong>, In-2-LF<br />
In-2-LF]<br />
N Anthrax Lethal Factor Protease<br />
<strong>Inhibitor</strong> III<br />
More online... www.calbiochem.com/inhibitors/ALF<br />
A cell-permeable N-acetylated, C-hydroxamate derivative of a 4-mer<br />
peptide designed from the MEK-2 template that acts as a competitive<br />
inhibitor of anthrax lethal factor (LF) metalloprotease (K = nM).<br />
i<br />
Also inhibits MEK-3 cleavage. Protects against anthrax toxin induced<br />
cytotoxicity in RAW264.7 and J772.A cells.<br />
176910 [BI-11B3; 5-(5-(2-Chloro-5-trifluoromethyl-phenyl)-furan-2ylmethylene)-4-oxo-2-thioxo-thiazolidin-3-yl)-acetic<br />
acid]<br />
A cell-permeable, rhodanine-acetic acid analog that chelates the<br />
active site Zn2+ and acts as a potent inhibitor of anthrax lethal factor<br />
(LF) metalloproteinase (K = 32 nM). Exhibits only minimal inhibition of<br />
i<br />
MMP-2 and MMP-9. Shown to effectively prevent LF-induced MAPKK<br />
proteolysis (< 2 mM) and offer protection against LF and protective<br />
antigen (PA) cytotoxic effects in RAW264.7 cells (IC < 5 mM). In<br />
50<br />
combination with the antibiotic ciprofloxacin, doubly enhances the<br />
survival rates of mice challenged with anthrax spores.<br />
5 mg $ 29<br />
Technical Support<br />
Phone 800 628 8470<br />
E-mail calbiochem@emdbiosciences.com<br />
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