Advances in the Development of SARS-CoV-2 Mpro Inhibitors |
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Authors: | Laura Agost-Beltrá n,Sergio de la Hoz-Rodrí guez,Lledó Bou-Iserte,Santiago Rodrí guez,Adriá n Ferná ndez-de-la-Pradilla,Florenci V. Gonzá lez |
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Affiliation: | 1.Departament de Química Inorgànica i Orgànica, Universitat Jaume I, 12080 Castelló, Spain; (L.A.-B.); (S.d.l.H.-R.); (L.B.-I.); (S.R.);2.Departament de Química Física i Analítica, Universitat Jaume I, 12080 Castelló, Spain; |
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Abstract: | Since the outbreak of COVID-19, one of the strategies used to search for new drugs has been to find inhibitors of the main protease (Mpro) of the virus SARS-CoV-2. Initially, previously reported inhibitors of related proteases such as the main proteases of SARS-CoV and MERS-CoV were tested. A huge effort was then carried out by the scientific community to design, synthesize and test new small molecules acting as inactivators of SARS-CoV-2 Mpro. From the chemical structure view, these compounds can be classified into two main groups: one corresponds to modified peptides displaying an adequate sequence for high affinity and a reactive warhead; and the second is a diverse group including chemical compounds that do not have a peptide framework. Although a drug including a SARS-CoV-2 main protease inhibitor has already been commercialized, denoting the importance of this field, more compounds have been demonstrated to be promising potent inhibitors as potential antiviral drugs. |
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Keywords: | COVID-19 main protease Mpro inhibitors |
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