1. Statine-based peptidomimetic compounds as inhibitors for SARS-CoV-2 main protease (SARS-CoV‑2 Mpro).
- Author
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Azevedo, Pedro Henrique R. de A., Camargo, Priscila G., Constant, Larissa E. C., Costa, Stephany da S., Silva, Celimar Sinézia, Rosa, Alice S., Souza, Daniel D. C., Tucci, Amanda R., Ferreira, Vivian N. S., Oliveira, Thamara Kelcya F., Borba, Nathalia R. R., Rodrigues, Carlos R., Albuquerque, Magaly G., Dias, Luiza R. S., Garrett, Rafael, Miranda, Milene D., Allonso, Diego, Lima, Camilo Henrique da S., and Muri, Estela Maris F.
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SARS-CoV-2 , *MOLECULAR dynamics , *HYDROGEN bonding interactions , *PEPTIDOMIMETICS , *CYTOTOXINS - Abstract
COVID-19 is a multisystemic disease caused by the SARS-CoV-2 airborne virus, a member of the Coronaviridae family. It has a positive sense single-stranded RNA genome and encodes two non-structural proteins through viral cysteine-proteases processing. Blocking this step is crucial to control virus replication. In this work, we reported the synthesis of 23 statine-based peptidomimetics to determine their ability to inhibit the main protease (Mpro) activity of SARS-CoV-2. Among the 23 peptidomimetics, 15 compounds effectively inhibited Mpro activity by 50% or more, while three compounds (7d, 8e, and 9g) exhibited maximum inhibition above 70% and IC50 < 1 µM. Compounds 7d, 8e, and 9g inhibited roughly 80% of SARS-CoV-2 replication and proved no cytotoxicity. Molecular docking simulations show putative hydrogen bond and hydrophobic interactions between specific amino acids and these inhibitors. Molecular dynamics simulations further confirmed the stability and persisting interactions in Mpro's subsites, exhibiting favorable free energy binding (ΔGbind) values. These findings suggest the statine-based peptidomimetics as potential therapeutic agents against SARS-CoV-2 by targeting Mpro. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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