# Bioactive Polyphenolic Compounds Showing Strong Antiviral Activities against Severe Acute Respiratory Syndrome Coronavirus 2

**Authors:** Ahmed Kandeil, Ahmed Mostafa, Omnia Kutkat, Yassmin Moatasim, Ahmed A. Al-Karmalawy, Adel A. Rashad, Ahmed E. Kayed, Azza E. Kayed, Rabeh El-Shesheny, Ghazi Kayali, Mohamed A. Ali

PMC · DOI: 10.3390/pathogens10060758 · Pathogens · 2021-06-15

## TL;DR

This study shows that curcumin, hesperidin, and quercetin may help fight SARS-CoV-2 by inhibiting virus replication and acting as potential Mpro inhibitors.

## Contribution

The study provides new evidence that these polyphenolic compounds have antiviral effects against SARS-CoV-2 in vitro and in silico.

## Key findings

- Curcumin, hesperidin, and quercetin significantly inhibited SARS-CoV-2 replication in Vero E6 cells.
- Molecular docking suggests these compounds may act as SARS-CoV-2 Mpro inhibitors.
- The compounds showed potential activity at the early stage of viral infection as virucidal agents.

## Abstract

Until now, there has been no direct evidence of the effectiveness of repurposed FDA-approved drugs against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infections. Although curcumin, hesperidin, and quercetin have broad spectra of pharmacological properties, their antiviral activities against SARS-CoV-2 remain unclear. Our study aimed to assess the in vitro antiviral activities of curcumin, hesperidin, and quercetin against SARS-CoV-2 compared to hydroxychloroquine and determine their mode of action. In Vero E6 cells, these compounds significantly inhibited virus replication, mainly as virucidal agents primarily indicating their potential activity at the early stage of viral infection. To investigate the mechanism of action of the tested compounds, molecular docking studies were carried out against both SARS-CoV-2 spike (S) and main protease (Mpro) receptors. Collectively, the obtained in silico and in vitro findings suggest that the compounds could be promising SARS-CoV-2 Mpro inhibitors. We recommend further preclinical and clinical studies on the studied compounds to find a potential therapeutic targeting COVID-19 in the near future.

## Linked entities

- **Chemicals:** curcumin (PubChem CID 969516), hesperidin (PubChem CID 10621), quercetin (PubChem CID 5280343), hydroxychloroquine (PubChem CID 3652)
- **Diseases:** Severe Acute Respiratory Syndrome Coronavirus 2 (MONDO:0100096), SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** Mpro [NCBI Gene 8673700], S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** COVID-19 (MESH:D000086382), CPE (MESH:D065606), viral infection (MESH:D014777), diabetes (MESH:D003920), respiratory illness (MESH:D012140), inflammation (MESH:D007249), Hepatitis C virus (MESH:D006526), influenza (MESH:D007251), Infectious Diseases (MESH:D003141), hyperlipidemia (MESH:D006949), coronavirus disease (MESH:D018352), Cytotoxicity (MESH:D064420), deaths (MESH:D003643), HBV (MESH:D006509), infection (MESH:D007239)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676], Curcuma longa (turmeric, species) [taxon 136217], Citrus (genus) [taxon 2706], Orthomyxoviridae (family) [taxon 11308]
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), Vero E6 — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0574)

## Full text

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## Figures

21 figures with captions in the complete paper: https://tomesphere.com/paper/PMC8232731/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC8232731/full.md

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Source: https://tomesphere.com/paper/PMC8232731