314082-72-9Relevant academic research and scientific papers
Highly potent and selective peptide-based inhibitors of the hepatitis C virus serine protease: Towards smaller inhibitors
Llinas-Brunet, Montse,Bailey, Murray,Fazal, Gulrez,Ghiro, Elise,Gorys, Vida,Goulet, Sylvie,Halmos, Ted,Maurice, Roger,Poirier, Martin,Poupart, Marc-Andre,Rancourt, Jean,Thibeault, Diane,Wernic, Dominik,Lamarre, Daniel
, p. 2267 - 2270 (2007/10/03)
Structure-activity studies on a hexapeptide N-terminal cleavage product of a dodecamer substrate led to the identification of very potent and highly specific inhibitors of the HCV NS3 protease/NS4A cofactor peptide complex. The largest increase in potency
