Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. Part 7: Structure–Activity Studies of Bicyclic 2-Pyridone-Containing Peptidomimetics

This publication has 41 references indexed in Scilit:

• Poliovirus‐encoded proteinase 3C: a possible evolutionary link between cellular serine and cysteine proteinase families
  Published by Wiley ,2001
• Recent advances in the development of human rhinovirus 3C protease inhibitors
  Expert Opinion on Therapeutic Patents, 2001
• Structure of human rhinovirus 3C protease reveals a trypsin-like polypeptide fold, RNA-binding site, and means for cleaving precursor polyprotein
  Cell, 1994
• Picornaviral 3C cysteine proteinases have a fold similar to chymotrypsin-like serine proteinases
  Nature, 1994
• TREATMENT OF THE PICORNA VIRUS COMMON COLD BY INHIBITORS OF VIRAL UNCOATING AND ATTACHMENT
  Annual Review of Microbiology, 1992
• Hydrolysis of a Series of Synthetic Peptide Substrates by the Human Rhinovirus 14 3C Proteinase, Cloned and Expressed in Escherichia coli
  Journal of General Virology, 1989
• Viral cysteine proteases are homologous to the trypsin-like family of serine proteases: structural and functional implications.
  Proceedings of the National Academy of Sciences, 1988
• VIRAL PROTEINASES
  Annual Review of Biochemistry, 1988
• RHINOVIRUS COLDS
  British Medical Bulletin, 1985
• Rhinoviruses
  Published by Springer Nature ,1982