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Inhibition of Dengue virus and West Nile virus proteases by click chemistry-derived benz[d]isothiazol-3(2H)-one derivatives
- Source :
- Bioorganic & Medicinal Chemistry. 20:1213-1221
- Publication Year :
- 2012
- Publisher :
- Elsevier BV, 2012.
-
Abstract
- Two click chemistry-derived focused libraries based on the benz[d]isothiazol-3(2H)-one scaffold were synthesized and screened against Dengue virus and West Nile virus NS2B-NS3 proteases. Several compounds (4l, 7j–n) displayed noteworthy inhibitory activity toward Dengue virus NS2B-NS3 protease in the absence and presence of added detergent. These compounds could potentially serve as a launching pad for a hit-to-lead optimization campaign.
- Subjects :
- Models, Molecular
Proteases
West Nile virus
viruses
medicine.medical_treatment
Clinical Biochemistry
Pharmaceutical Science
Dengue virus
Biology
medicine.disease_cause
Antiviral Agents
Biochemistry
Article
Dengue fever
Dengue
Drug Discovery
medicine
Humans
Protease Inhibitors
Molecular Biology
Protease
Organic Chemistry
Dengue Virus
medicine.disease
Virology
Thiazoles
Peptide Hydrolases
Click chemistry
Molecular Medicine
Click Chemistry
West Nile Fever
Subjects
Details
- ISSN :
- 09680896
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....494f71a754ca464d52c1d0ffbb2a8ab4
- Full Text :
- https://doi.org/10.1016/j.bmc.2011.12.047