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Synthesis and evaluation of isatin derivatives as effective SARS coronavirus 3CL protease inhibitors.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2005 Jun 15; Vol. 15 (12), pp. 3058-62. - Publication Year :
- 2005
-
Abstract
- N-Substituted isatin derivatives were prepared from the reaction of isatin and various bromides via two steps. Bioactivity assay results (in vitro tests) demonstrated that some of these compounds are potent and selective inhibitors against SARS coronavirus 3CL protease with IC50 values ranging from 0.95 to 17.50 microM. Additionally, isatin 4o exhibited more potent inhibition for SARS coronavirus protease than for other proteases including papain, chymotrypsin, and trypsin.
- Subjects :
- Binding Sites
Chymotrypsin pharmacology
Computer Simulation
Coronavirus 3C Proteases
Cysteine Endopeptidases
Endopeptidases
Enzyme Activation
Fluorescence Resonance Energy Transfer
Humans
Isatin chemical synthesis
Molecular Structure
Papain pharmacology
Protease Inhibitors chemistry
Structure-Activity Relationship
Substrate Specificity
Trypsin pharmacology
Isatin analogs & derivatives
Isatin pharmacology
Protease Inhibitors chemical synthesis
Protease Inhibitors pharmacology
Severe acute respiratory syndrome-related coronavirus enzymology
Viral Proteins antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 0960-894X
- Volume :
- 15
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 15896959
- Full Text :
- https://doi.org/10.1016/j.bmcl.2005.04.027