Title of article :
Inhibition of trypsin and urokinase by Cbz-amino(4-guanidinophenyl)methanephosphonate aromatic ester derivatives: The influence of the ester group on their biological activity
Author/Authors :
Marcin Sie?czyk، نويسنده , , Jozef Oleksyszyn، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Abstract :
The urokinase plasminogen activator is a trypsin-like serine protease, important in tumor development. Here, we report the synthesis and biochemical evaluation of selective and potent diaryl esters of phosphonic-type inhibitors for urokinase. We have found that the substituted phenyl ester ring has a strong influence on the inhibitory activity of these compounds. This led to the most potent phosphonic inhibitor for uPA synthesized to date.
Keywords :
?-Aminoalkylphosphonates , Arginine mimetics , Trypsin-like serine protease inhibitors , urokinase
Journal title :
Bioorganic & Medicinal Chemistry Letters
Journal title :
Bioorganic & Medicinal Chemistry Letters