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author Drayman, Nir
DeMarco, Jennifer K.
Jones, Krysten A.
Azizi, Saara-Anne
Froggatt, Heather M.
Tan, Kemin
Maltseva, Natalia Ivanovna
Chen, Siquan
Nicolaescu, Vlad
Dvorkin, Steve
Furlong, Kevin
Kathayat, Rahul S.
Firpo, Mason R.
Mastrodomenico, Vincent
Bruce, Emily A.
Schmidt, Madaline M.
Jedrzejczak, Robert
Muñoz-Alía, Miguel Á.
Schuster, Brooke
Nair, Vishnu
Han, Kyu-yeon
O’Brien, Amornrat
Tomatsidou, Anastasia
Meyer, Bjoern
Vignuzzi, Marco
Missiakas, Dominique
Botten, Jason W.
Brooke, Christopher B.
Lee, Hyun
Baker, Susan C.
Mounce, Bryan C.
Heaton, Nicholas S.
Severson, William E.
Palmer, Kenneth E.
Dickinson, Bryan C.
Joachimiak, Andrzej
Randall, Glenn
Tay, Savaş
author_facet Drayman, Nir
DeMarco, Jennifer K.
Jones, Krysten A.
Azizi, Saara-Anne
Froggatt, Heather M.
Tan, Kemin
Maltseva, Natalia Ivanovna
Chen, Siquan
Nicolaescu, Vlad
Dvorkin, Steve
Furlong, Kevin
Kathayat, Rahul S.
Firpo, Mason R.
Mastrodomenico, Vincent
Bruce, Emily A.
Schmidt, Madaline M.
Jedrzejczak, Robert
Muñoz-Alía, Miguel Á.
Schuster, Brooke
Nair, Vishnu
Han, Kyu-yeon
O’Brien, Amornrat
Tomatsidou, Anastasia
Meyer, Bjoern
Vignuzzi, Marco
Missiakas, Dominique
Botten, Jason W.
Brooke, Christopher B.
Lee, Hyun
Baker, Susan C.
Mounce, Bryan C.
Heaton, Nicholas S.
Severson, William E.
Palmer, Kenneth E.
Dickinson, Bryan C.
Joachimiak, Andrzej
Randall, Glenn
Tay, Savaş
author_sort Drayman, Nir
collection PubMed
description There is an urgent need for antiviral agents that treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. We screened a library of 1900 clinically safe drugs against OC43, a human beta coronavirus that causes the common cold, and evaluated the top hits against SARS-CoV-2. Twenty drugs significantly inhibited replication of both viruses in cultured human cells. Eight of these drugs inhibited the activity of the SARS-CoV-2 main protease, 3CLpro, with the most potent being masitinib, an orally bioavailable tyrosine kinase inhibitor. X-ray crystallography and biochemistry show that masitinib acts as a competitive inhibitor of 3CLpro. Mice infected with SARS-CoV-2 and then treated with masitinib showed >200-fold reduction in viral titers in the lungs and nose, as well as reduced lung inflammation. Masitinib was also effective in vitro against all tested variants of concern (B.1.1.7, B.1.351, and P.1).
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spelling pubmed-88090562022-02-02 Masitinib is a broad coronavirus 3CL inhibitor that blocks replication of SARS-CoV-2 Drayman, Nir DeMarco, Jennifer K. Jones, Krysten A. Azizi, Saara-Anne Froggatt, Heather M. Tan, Kemin Maltseva, Natalia Ivanovna Chen, Siquan Nicolaescu, Vlad Dvorkin, Steve Furlong, Kevin Kathayat, Rahul S. Firpo, Mason R. Mastrodomenico, Vincent Bruce, Emily A. Schmidt, Madaline M. Jedrzejczak, Robert Muñoz-Alía, Miguel Á. Schuster, Brooke Nair, Vishnu Han, Kyu-yeon O’Brien, Amornrat Tomatsidou, Anastasia Meyer, Bjoern Vignuzzi, Marco Missiakas, Dominique Botten, Jason W. Brooke, Christopher B. Lee, Hyun Baker, Susan C. Mounce, Bryan C. Heaton, Nicholas S. Severson, William E. Palmer, Kenneth E. Dickinson, Bryan C. Joachimiak, Andrzej Randall, Glenn Tay, Savaş Science Reports There is an urgent need for antiviral agents that treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. We screened a library of 1900 clinically safe drugs against OC43, a human beta coronavirus that causes the common cold, and evaluated the top hits against SARS-CoV-2. Twenty drugs significantly inhibited replication of both viruses in cultured human cells. Eight of these drugs inhibited the activity of the SARS-CoV-2 main protease, 3CLpro, with the most potent being masitinib, an orally bioavailable tyrosine kinase inhibitor. X-ray crystallography and biochemistry show that masitinib acts as a competitive inhibitor of 3CLpro. Mice infected with SARS-CoV-2 and then treated with masitinib showed >200-fold reduction in viral titers in the lungs and nose, as well as reduced lung inflammation. Masitinib was also effective in vitro against all tested variants of concern (B.1.1.7, B.1.351, and P.1). American Association for the Advancement of Science 2021-08-20 2021-07-20 /pmc/articles/PMC8809056/ /pubmed/34285133 http://dx.doi.org/10.1126/science.abg5827 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reports
Drayman, Nir
DeMarco, Jennifer K.
Jones, Krysten A.
Azizi, Saara-Anne
Froggatt, Heather M.
Tan, Kemin
Maltseva, Natalia Ivanovna
Chen, Siquan
Nicolaescu, Vlad
Dvorkin, Steve
Furlong, Kevin
Kathayat, Rahul S.
Firpo, Mason R.
Mastrodomenico, Vincent
Bruce, Emily A.
Schmidt, Madaline M.
Jedrzejczak, Robert
Muñoz-Alía, Miguel Á.
Schuster, Brooke
Nair, Vishnu
Han, Kyu-yeon
O’Brien, Amornrat
Tomatsidou, Anastasia
Meyer, Bjoern
Vignuzzi, Marco
Missiakas, Dominique
Botten, Jason W.
Brooke, Christopher B.
Lee, Hyun
Baker, Susan C.
Mounce, Bryan C.
Heaton, Nicholas S.
Severson, William E.
Palmer, Kenneth E.
Dickinson, Bryan C.
Joachimiak, Andrzej
Randall, Glenn
Tay, Savaş
Masitinib is a broad coronavirus 3CL inhibitor that blocks replication of SARS-CoV-2
title Masitinib is a broad coronavirus 3CL inhibitor that blocks replication of SARS-CoV-2
title_full Masitinib is a broad coronavirus 3CL inhibitor that blocks replication of SARS-CoV-2
title_fullStr Masitinib is a broad coronavirus 3CL inhibitor that blocks replication of SARS-CoV-2
title_full_unstemmed Masitinib is a broad coronavirus 3CL inhibitor that blocks replication of SARS-CoV-2
title_short Masitinib is a broad coronavirus 3CL inhibitor that blocks replication of SARS-CoV-2
title_sort masitinib is a broad coronavirus 3cl inhibitor that blocks replication of sars-cov-2
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809056/
https://www.ncbi.nlm.nih.gov/pubmed/34285133
http://dx.doi.org/10.1126/science.abg5827
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