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Synthesis and antiviral activity of substituted bisaryl amide compounds as novel influenza virus inhibitors. | LitMetric

AI Article Synopsis

  • The influenza virus consistently causes illness and death each year, making it a crucial focus for drug development.
  • Researchers discovered a new class of compounds called substituted bisaryl amides that may serve as anti-influenza agents and tested them for their effectiveness.
  • Among the compounds, 1j showed significant antiviral activity against multiple strains of the influenza virus, including some that are resistant to existing treatments, indicating its potential as a candidate for further research.

Article Abstract

The influenza virus is a persistent cause of mortality and morbidity on an annual basis and thus presents itself as an important target for pharmaceutical investigation. In this work, substituted bisaryl amide compounds were found to be a new class of potential anti-influenza agents, and a series of substituted bisaryl amide compounds were synthesised and evaluated for their anti-influenza virus activities. The analysis of the results produced a preliminary structure-activity relationship study (SAR). Compounds 1a, 1g, 1h, 1j, 1l and 1n exhibited clear antiviral activities against the influenza A (A/Guangdong Luohu/219/2006, H1N1) virus with 50% inhibitory concentrations (IC(50)) for virus growth ranging from 12.5 to 59.0 μM. Specifically, compound 1j also possessed antiviral activity against both oseltamivir-resistant influenza (A/Jinnan/15/2009) virus and influenza B (B/Jifang/13/97) virus with IC(50) values of 9.2 μM and 21.4 μM, respectively. Compound 1j is thus worth further investigation as an anti-influenza virus candidate.

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Source
http://dx.doi.org/10.1016/j.ejmech.2012.07.008DOI Listing

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