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Discovery of novel SARS-CoV-2 inhibitors targeting the main protease M(pro) by virtual screenings and hit optimization
Two years after its emergence, SARS-CoV-2 still represents a serious and global threat to human health. Antiviral drug development usually takes a long time and, to increase the chances of success, chemical variability of hit compounds represents a valuable source for the discovery of new antivirals...
Autores principales: | Mercorelli, Beatrice, Desantis, Jenny, Celegato, Marta, Bazzacco, Alessandro, Siragusa, Lydia, Benedetti, Paolo, Eleuteri, Michela, Croci, Federico, Cruciani, Gabriele, Goracci, Laura, Loregian, Arianna |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172283/ https://www.ncbi.nlm.nih.gov/pubmed/35688349 http://dx.doi.org/10.1016/j.antiviral.2022.105350 |
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