4.7 Article

Garcinia cambogia Phenolics as Potent Anti-COVID-19 Agents: Phytochemical Profiling, Biological Activities, and Molecular Docking

Journal

PLANTS-BASEL
Volume 11, Issue 19, Pages -

Publisher

MDPI
DOI: 10.3390/plants11192521

Keywords

Garcinia cambogia; anti-COVID-19; 3CL-pro; molecular docking; chemical profiling

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Funding

  1. King Saud University, Riyadh, Saudi Arabia [RSP2022R504]

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COVID-19 is a disease caused by the coronavirus SARS-CoV-2 and became a pandemic in a critically short time. In this study, a metabolomics analysis of the Garcinia cambogia Roxb. fruit rind was conducted, leading to the isolation of eight known compounds. Among them, naringin showed potent antiviral activity and molecular docking studies revealed its interaction with the COVID-19 protease enzyme.
COVID-19 is a disease caused by the coronavirus SARS-CoV-2 and became a pandemic in a critically short time. Phenolic secondary metabolites attracted much attention from the pharmaceutical industries for their easily accessible natural sources and proven antiviral activity. In our mission, a metabolomics study of the Garcinia cambogia Roxb. fruit rind was performed using LC-HRESIMS to investigate its chemical profile, especially the polar aspects, followed by a detailed phytochemical analysis, which led to the isolation of eight known compounds. Using spectrometric techniques, the isolated compounds were identified as quercetin, amentoflavone, vitexin, rutin, naringin, catechin, p-coumaric, and gallic acids. The antiviral activities of the isolated compounds were investigated using two assays; the 3CL-M-pro enzyme showed that naringin had a potent effect with IC50 16.62 mu g/mL, followed by catechin and gallic acid (IC50 26.2, 30.35 mu g/mL, respectively), while the direct antiviral inhibition effect of naringin confirmed the potency with an EC50 of 0.0169 mu M. To show the molecular interaction, in situ molecular docking was carried out using a COVID-19 protease enzyme. Both biological effects and docking studies showed the hydrophobic interactions with Gln 189 or Glu 166, per the predicated binding pose of the isolated naringin.

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