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Natural product-derived phytochemicals as potential agents against coronaviruses: A review. | LitMetric

Natural product-derived phytochemicals as potential agents against coronaviruses: A review.

Virus Res

School of Health, Medical and Applied Sciences, CQUniversity, Bruce Hwy, North Rockhampton, QLD, Australia; Centre for Indigenous Health Equity Research, CQUniversity, Bruce Hwy, North Rockhampton, QLD, Australia. Electronic address:

Published: July 2020

AI Article Synopsis

  • Coronaviruses, including SARS, MERS, and COVID-19, pose significant health and economic challenges, with few effective antiviral treatments available.
  • Natural compounds may offer potential therapeutic alternatives, as many have antiviral properties and chemical diversity.
  • Research has identified specific natural compounds like scutellarein and quercetin, particularly those with fused ring structures, as promising candidates for inhibiting coronavirus infections.

Article Abstract

Coronaviruses are responsible for a growing economic, social and mortality burden, as the causative agent of diseases such as severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), avian infectious bronchitis virus (IBV) and COVID-19. However, there is a lack of effective antiviral agents for many coronavirus strains. Naturally existing compounds provide a wealth of chemical diversity, including antiviral activity, and thus may have utility as therapeutic agents against coronaviral infections. The PubMed database was searched for papers including the keywords coronavirus, SARS or MERS, as well as traditional medicine, herbal, remedy or plants, with 55 primary research articles identified. The overwhelming majority of publications focussed on polar compounds. Compounds that show promise for the inhibition of coronavirus in humans include scutellarein, silvestrol, tryptanthrin, saikosaponin B, quercetin, myricetin, caffeic acid, psoralidin, isobavachalcone, and lectins such as griffithsin. Other compounds such as lycorine may be suitable if a therapeutic level of antiviral activity can be achieved without exceeding toxic plasma concentrations. It was noted that the most promising small molecules identified as coronavirus inhibitors contained a conjugated fused ring structure with the majority being classified as being polyphenols.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190535PMC
http://dx.doi.org/10.1016/j.virusres.2020.197989DOI Listing

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