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• W4220784032 abstract "Thirty-two clofazimine derivatives, of which twenty-two were new, were synthesized and evaluated for their antiviral effects against both rabies virus and pseudo-typed SARS-CoV-2, taking clofazimine (1) as the lead. Among them, compound 15f bearing 4-methoxy-2-pyridyl at the N5-position showed superior or comparable antiviral activities to lead 1, with the EC50 values of 1.45 μM and 14.6 μM and the SI values of 223 and 6.1, respectively. Compound 15f inhibited rabies and SARS-CoV-2 by targeting G or S protein to block membrane fusion, as well as binding to L protein or nsp13 to inhibit intracellular biosynthesis respectively, and thus synergistically exerted a broad-spectrum antiviral effect. The results provided useful scientific data for the development of clofazimine derivatives into a new class of broad-spectrum antiviral candidates." @default.
• W4220784032 created "2022-04-03" @default.
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• W4220784032 date "2022-04-01" @default.
• W4220784032 modified "2023-10-17" @default.
• W4220784032 title "Clofazimine derivatives as potent broad-spectrum antiviral agents with dual-target mechanism" @default.
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• W4220784032 doi "https://doi.org/10.1016/j.ejmech.2022.114209" @default.
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