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Updated: Nov 8, 2025

High-throughput Screening for Broad-spectrum Chemical Inhibitors of RNA Viruses
Published on: May 5, 2014
Potential Candidates against COVID-19 Targeting RNA-Dependent RNA Polymerase: A Comprehensive Review
1Institute of Pharmaceutical Research, GLA University, Mathura, 281406, U.P., India.
Abstract:
Due to the extremely contagious nature of SARS-COV-2, it presents a significant threat to humans worldwide. A plethora of studies are going on all over the world to discover the drug to fight SARS-COV-2. One of the most promising targets is RNA-dependent RNA polymerase (RdRp), responsible for viral RNA replication in host cells. Since RdRp is a viral enzyme with no host cell homologs, it allows the development of selective SARS-COV-2 RdRp inhibitors. A variety of studies used in silico approaches for virtual screening, molecular docking, and repurposing of already existing drugs and phytochemicals against SARS-COV-2 RdRp. This review focuses on collating compounds possessing the potential to inhibit SARS-COV-2 RdRp based on in silico studies to give medicinal chemists food for thought so that the existing drugs can be repurposed for the control and treatment of ongoing COVID-19 pandemic after performing in vitro and in vivo experiments.
Insights
Researchers reviewed in silico studies to identify potential inhibitors of SARS-COV-2 RNA-dependent RNA polymerase (RdRp). This review aims to guide drug repurposing for COVID-19 treatment.
Area of Science:
- * Virology and Drug Discovery
- * Computational Chemistry and Cheminformatics
Background:
- * Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-COV-2) is a highly contagious virus causing a global health threat.
- * The viral RNA-dependent RNA polymerase (RdRp) is crucial for viral replication and a promising target for antiviral drug development.
- * RdRp's lack of human homologs enables the design of selective inhibitors, minimizing host cell toxicity.
Purpose of the Study:
- * To compile and review in silico studies identifying potential inhibitors of SARS-COV-2 RdRp.
- * To provide a resource for medicinal chemists to accelerate drug repurposing for COVID-19.
- * To highlight compounds with potential for further in vitro and in vivo validation.
Main Methods:
- * Comprehensive literature search for in silico studies (virtual screening, molecular docking).
- * Analysis of studies focusing on drug repurposing and phytochemical screening against SARS-COV-2 RdRp.
- * Collating identified compounds with inhibitory potential against the target enzyme.
Main Results:
- * Multiple existing drugs and phytochemicals have shown potential as SARS-COV-2 RdRp inhibitors through in silico analyses.
- * In silico approaches effectively screened large compound libraries and identified promising candidates for drug repurposing.
- * The reviewed studies provide a foundation for experimental validation of these compounds.
Conclusions:
- * In silico studies offer a rapid and cost-effective method for identifying potential SARS-COV-2 RdRp inhibitors.
- * Drug repurposing of identified compounds could expedite the development of treatments for COVID-19.
- * Further in vitro and in vivo studies are essential to confirm the efficacy and safety of these potential inhibitors.
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