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Innovative Medicines & Omics                                           SARS-CoV-2 inhibition by quinolines



            coronaviridae viruses, including MERS-CoV and SARS-  88887.694990/2022-00, 88887.719751/2022-00), and FAPERJ
            CoV.  This cross-viral activity prompted investigations   (E-26/201.426/2022, E-26/203.183/2023). The authors would
                74
            into lopinavir’s capability against SARS-CoV-2, showing   also like to thank CAPES (process 88887.506710/2020-00,
            promising  in vitro efficacy against viral proteases such   88887.647774/2021-00 and 88887.722759/2022-00) and
                pro 75
            as M .  Given these properties, lopinavir was selected   CNPq (process 312295/2020-0).
            as a positive control in this study, highlighting its potent
            protease inhibition.                               Conflict of interest
              Therefore, through the docking analyses using diverse   The authors declare that they have no competing interests.
            software tools and various protein conformations, it has
            become possible to evaluate the inhibitory capacity of   Author contributions
            the  studied  compounds  and,  consequently,  it  has  been   Conceptualization: Adilson D. da Silva, Priscila Vanessa S.
            determined that these compounds possess substantial   Zabala Capriles, Milene Dias Miranda
            potential as promising agents in the fight against SARS-  Investigation: Adilson D. da Silva, Priscila Vanessa S. Zabala
            CoV-2.                                                Capriles, Milene Dias Miranda
                                                               Methodology:  Nícolas Glanzmann, Vinicius Carius de
            5. Conclusion                                         Souza, Thamara Kelcya F. Oliveira, Amanda R. Tucci,

            Based on the chemical structure of our molecules, the   Eduarda Alves Penna, Matheus José Novais Landim,
            results of this study indicate that the action of Q1a – Q4a,   Alice Santos Rosa, Maria Luiza Pereira Baltazar,
            Q1b – Q4b, and Q1bS compounds can directly interfere   Vivian Neuza S. Ferreira, Pamella Constantino-Teles,
            with  the  entry  process  of  SARS-CoV-2  into the  target   Daniel Dias Coutinho Souza, Sylvia Roxo, Caroline
            cell. Among all compounds,  Q4b  distinguished itself by   Souza de Freitas, Aline de Paula Dias da Silva, Thiago
            demonstrating the most favorable overall results, showing   Moreno Lopes Souza
            low cytotoxicity and a selectivity index above 90. Thus,   Writing – original draft: Nícolas Glanzmann, Thamara
            our data are promising and expand knowledge about new   Kelcya F. Oliveira,  Vinicius Carius de Souza,  Maria
            therapeutic agents in the  fight against COVID-19. We   Luiza Pereira Baltazar, Matheus José Novais Landim,
            believe that further efforts are needed to understand the   Priscila Vanessa S. Zabala Capriles
            mechanism of action by this group of quinolines, as well as   Writing – review & editing: Nícolas Glanzmann, Priscila
            their performance in animal infection models.         Vanessa S. Zabala Capriles, Milene Dias Miranda

            Acknowledgments                                    Ethics approval and consent to participate
            Thanks are due to Biosafety Level 3 (BSL3) laboratory facility   Not applicable.
            in Pavilhão Leonidas Deane, Instituto Oswaldo Cruz.   Consent for publication
            Fiocruz, RJ; and Andre Sampaio from Farmanguinhos,
            platform RPT11M, for kindly donating the Calu-3 cells.  Not applicable.
            Funding                                            Availability of data

            This research was funded by the Coordenação de     Data are available from the corresponding author upon
            Aperfeiçoamento de Pessoal de Nível Superior (CAPES),   reasonable request.
            Conselho Nacional de Desenvolvimento Científico e
            Tecnológico (CNPq), Fundação de Amparo à Pesquisa   References
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            Volume 1 Issue 1 (2024)                        102                               doi: 10.36922/imo.3442
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