Article ID Journal Published Year Pages File Type
10594621 Bioorganic & Medicinal Chemistry Letters 2012 5 Pages PDF
Abstract
Produced by Staphylococcus aureus, SplB belongs to the chymotrypsin-like serine protease family. Since the biological role of SplB protease is unknown, the design and application of its specific inhibitors may help to reveal the function of this enzyme. Until now no SplB inhibitors have been reported. Herein, we present the design and synthesis of novel α-aminophosphonic analogues of glutamine, as well as their peptidyl derivatives. The inhibitory effects of these compounds towards the newly discovered SplB serine protease from S. aureus are characterized. We have also investigated the influence of aromatic ester substituents on inhibitory potency towards SplB. One of the compounds-Cbz-Glu-Leu-GlnP(OC6H4-4-O-CH3)2-displayed an apparent second-order inhibition rate value of 1400 M−1 s−1.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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