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Live Imaging and Quantification of Viral Infection in K18 hACE2 Transgenic Mice Using Reporter-Expressing Recombinant SARS-CoV-2
Published on: November 5, 2021
COVID-19 treatment: Much research and testing, but far, few magic bullets against SARS-CoV-2 coronavirus
1Laboratorio de Química Orgánica y Biomolecular, CMN, Universidad Industrial de Santander, Parque Tecnológico Guatiguará, Piedecuesta, 681011, Colombia.
Abstract:
The new virus of the of β-Coronaviruses genus, SARS-CoV-2, is the causative agent of coronavirus disease-2019 (COVID-19) and is winning a proverbial chess match against all players simultaneous, including physicians, clinicians, pathologists, doctors, scientists, economists, athletes and politicians. The COVID-19 outbreak has seriously threatened public health, killing the most vulnerable persons and causing general panic. To stop this disease, effective remedies (i.e., drugs, vaccines, personal protection elements, etc.) are urgently required. Unfortunately, no registered specific therapies (including antiviral therapies, immune-modulating agents and vaccines) are currently available to treat coronavirus infections, highlighting an urgent need for therapeutics targeting SARS-CoV-2. In this work, fourteen existing small molecule drugs or/and experimental drugs selected by experts and examined from the point of view of bioavailability via the Lipinski-Veber rules and assessment of their physicochemical descriptors. The aim of this study is to discover selected pattern similarities and peculiar characteristics that could be useful for antiviral drug optimization, drug combination or new antiviral agent design.
Insights
This study evaluates fourteen drugs for treating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by assessing bioavailability and physicochemical properties. Findings may aid in optimizing antiviral drug design and combination therapies for coronavirus disease 2019 (COVID-19).
Area of Science:
- Virology
- Medicinal Chemistry
- Drug Discovery
Background:
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19), a global health crisis.
- The lack of specific antiviral therapies necessitates urgent development of effective treatments.
- Existing small molecule drugs and experimental compounds are being investigated for potential therapeutic use.
Purpose of the Study:
- To evaluate fourteen selected small molecule drugs for their potential against SARS-CoV-2.
- To assess the bioavailability and physicochemical properties of these candidate drugs.
- To identify patterns and characteristics beneficial for antiviral drug optimization and new agent design.
Main Methods:
- Expert selection of fourteen existing or experimental small molecule drugs.
- Application of Lipinski’s Rule of Five and Veber’s rules for bioavailability assessment.
- Analysis of physicochemical descriptors to understand drug properties.
Main Results:
- Physicochemical descriptors and bioavailability were evaluated for selected drugs.
- Potential similarities and unique characteristics relevant to antiviral activity were identified.
- The study provides a basis for further drug optimization and development.
Conclusions:
- The evaluation of physicochemical properties and bioavailability is crucial for identifying potential SARS-CoV-2 therapeutics.
- Findings can inform the design of novel antiviral agents and optimized drug combinations.
- This research contributes to the urgent need for effective treatments against COVID-19.
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