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FEBS Lett ; 583(3): 549-55, 2009 Feb 04.
Article in English | MEDLINE | ID: mdl-19166843

ABSTRACT

Picornaviruses (PV) and coronaviruses (CoV) are positive-stranded RNA viruses which infect millions of people worldwide each year, resulting in a wide range of clinical outcomes. As reported in this study, using high throughput screening against approximately 6800 small molecules, we have identified several novel inhibitors of SARS-CoV 3CL(pro) with IC(50) of low microM. Interestingly, one of them equally inhibited both 3C(pro) and 3CL(pro) from PV and CoV, respectively. Using computer modeling, the structural features of these compounds as individual and common protease inhibitors were elucidated to enhance our knowledge for developing anti-viral agents against PV and CoV.


Subject(s)
Coronavirus/drug effects , Coronavirus/enzymology , Peptide Hydrolases/metabolism , Picornaviridae/drug effects , Picornaviridae/enzymology , Protease Inhibitors/chemistry , Protease Inhibitors/pharmacology , Amino Acid Sequence , Computer Simulation , Conserved Sequence , Drug Evaluation, Preclinical , Models, Molecular , Molecular Sequence Data , Peptide Hydrolases/chemistry , Protein Binding , Protein Structure, Tertiary , Sequence Alignment , Structure-Activity Relationship
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