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High-throughput Antiviral Assays to Screen for Inhibitors of Zika Virus Replication
Published on: October 30, 2021
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Progress and prospects on DENV protease inhibitors.
Ajay Kumar Timiri1, Barij Nayan Sinha1, Venkatesan Jayaprakash1
1Department of Pharmaceutical Sciences and Technology, Birla Institute of Technology, Mesra, Ranchi 835215, Jharkhand, India.
European Journal of Medicinal Chemistry
|April 20, 2016
Summary
Dengue fever is rising, necessitating new treatments. This review explores the dengue virus NS2B-NS3 protease, a key target for drug discovery, and surveys existing inhibitors.
Area of Science:
- Virology and Drug Discovery
- Medicinal Chemistry
Background:
- Dengue fever cases are increasing globally, particularly in tropical and subtropical regions.
- The dengue virus NS2B-NS3 protease is crucial for viral replication and a promising drug target.
- Protease inhibitors have shown success against viruses like HIV and HCV.
Purpose of the Study:
- To provide insights into the molecular mechanism of the dengue virus protease.
- To review current inhibitors targeting the dengue NS2B-NS3 protease from a medicinal chemistry perspective.
Main Methods:
- Literature review of published studies on dengue virus protease.
- Analysis of molecular mechanisms and inhibitor data.
Main Results:
- The NS2B-NS3 protease plays a vital role in polyprotein processing essential for viral genome replication.
- Various inhibitors targeting this protease have been reported, with potential for drug development.
Conclusions:
- Understanding the dengue protease mechanism and existing inhibitors is crucial for designing potent antiviral drugs.
- The NS2B-NS3 protease remains a high-priority target for novel dengue fever therapeutics.
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