Design and synthesis of dipeptidyl α′,β′-epoxy ketones, potent irreversible inhibitors of the cysteine protease cruzain
- 1 October 1998
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 8 (19) , 2809-2812
- https://doi.org/10.1016/s0960-894x(98)00494-6
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Cysteine Proteases and Their InhibitorsChemical Reviews, 1997
- Investigation of the substrate specificity of cruzipain, the major cysteine proteinase of Trypanosoma cruzi, through the use of cystatin-derived substrates and inhibitorsBiochemical Journal, 1996
- Chapter 26. Regulation of Apoptosis by Members of the ICE Family and the Bcl-2 FamilyPublished by Elsevier ,1996
- The Crystal Structure of Cruzain: A Therapeutic Target for Chagas' DiseaseJournal of Molecular Biology, 1995
- THE PROTEASES AND PATHOGENICITY OF PARASITIC PROTOZOAAnnual Review of Microbiology, 1993
- Peptide-fluoromethyl ketones arrest intracellular replication and intercellular transmission of Trypanosoma cruziMolecular and Biochemical Parasitology, 1993
- Crystal structure of papain-E64-c complex. Binding diversity of E64-c to papain S2 and S3 subsitesBiochemical Journal, 1992
- Refined x-ray structure of papain.E-64-c complex at 2.1-A resolutionPublished by Elsevier ,1991
- Papain Inhibitions by Optically Active E-64 AnalogsThe Journal of Biochemistry, 1981
- Structure and synthesis of E-64, a new thiol protease inhibitor.Agricultural and Biological Chemistry, 1978