TY - JOUR
T1 - Repurposing the HCV NS3-4A protease drug boceprevir as COVID-19 therapeutics
AU - Oerlemans, Rick
AU - Ruiz Moreno, Angel
AU - Cong, Ying-Ying
AU - Dinesh Kumar, Nilima
AU - Velasco-Velazquez, M.A.
AU - Neochoritis, Constantinos G.
AU - Smit, Jolanda
AU - Reggiori, Fulvio
AU - Groves, Matthew
AU - Dömling, Alex
N1 - This journal is © The Royal Society of Chemistry.
PY - 2021/3/1
Y1 - 2021/3/1
N2 - The rapid growth of COVID-19 cases is causing an increasing death toll and also paralyzing the world economy. De novo drug discovery takes years to move from idea and/or pre-clinic to market, and it is not a short-term solution for the current SARS-CoV-2 pandemic. Drug repurposing is perhaps the only short-term solution, while vaccination is a middle-term solution. Here, we describe the discovery path of the HCV NS3-4A protease inhibitors boceprevir and telaprevir as SARS-CoV-2 main protease (3CLpro) inhibitors. Based on our hypothesis that α-ketoamide drugs can covalently bind to the active site cysteine of the SARS-CoV-2 3CLpro, we performed docking studies, enzyme inhibition and co-crystal structure analyses and finally established that boceprevir, but not telaprevir, inhibits replication of SARS-CoV-2 and mouse hepatitis virus (MHV), another coronavirus, in cell culture. Based on our studies, the HCV drug boceprevir deserves further attention as a repurposed drug for COVID-19 and potentially other coronaviral infections as well.
AB - The rapid growth of COVID-19 cases is causing an increasing death toll and also paralyzing the world economy. De novo drug discovery takes years to move from idea and/or pre-clinic to market, and it is not a short-term solution for the current SARS-CoV-2 pandemic. Drug repurposing is perhaps the only short-term solution, while vaccination is a middle-term solution. Here, we describe the discovery path of the HCV NS3-4A protease inhibitors boceprevir and telaprevir as SARS-CoV-2 main protease (3CLpro) inhibitors. Based on our hypothesis that α-ketoamide drugs can covalently bind to the active site cysteine of the SARS-CoV-2 3CLpro, we performed docking studies, enzyme inhibition and co-crystal structure analyses and finally established that boceprevir, but not telaprevir, inhibits replication of SARS-CoV-2 and mouse hepatitis virus (MHV), another coronavirus, in cell culture. Based on our studies, the HCV drug boceprevir deserves further attention as a repurposed drug for COVID-19 and potentially other coronaviral infections as well.
U2 - 10.1039/D0MD00367K
DO - 10.1039/D0MD00367K
M3 - Article
C2 - 34041486
VL - 12
SP - 370
EP - 379
JO - RSC Medicinal Chemistry
JF - RSC Medicinal Chemistry
IS - 3
ER -