Azodicarboxamides: A New Class of Cysteine Proteinase Inhibitor for Hepatitis A Virus and Human Rhinovirus 3C Enzymes
- 1 December 1999
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (26) , 9538-9546
- https://doi.org/10.1021/jo9915123
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Formation of Nicotinamide from Nicotinuric Acid by Peptidylglycine α-Amidating Monooxygenase (PAM): A Possible Alternative Route from Nicotinic Acid (Niacin) to NADP in MammalsJournal of the American Chemical Society, 1999
- Azapeptides as Inhibitors and Active Site Titrants for Cysteine ProteinasesJournal of Medicinal Chemistry, 1998
- Foodborne outbreaks of hepatitis A in a low endemic country: an emerging problem?Epidemiology and Infection, 1998
- Synthesis, chemistry and conformational properties of piperazic acidsChemical Society Reviews, 1998
- Structure and Design of Potent and Selective Cathepsin K InhibitorsJournal of the American Chemical Society, 1997
- Inhibition of Human Placenta Glutathione Transferase Pl‐1 by the Antibiotic Calvatic Acid and its Diazocyanide AnalogueEuropean Journal of Biochemistry, 1997
- Small peptidic aldehyde inhibitors of human rhinovirus 3C proteaseBioorganic & Medicinal Chemistry Letters, 1996
- Peptide Aldehyde Inhibitors of Hepatitis A Virus 3C ProteinaseBiochemistry, 1995
- Hepatitis A virus 3C proteinase substrate specificityBiochemistry, 1992
- Expression and characterization of recombinant hepatitis A virus 3C proteinaseBiochemistry, 1992