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BioWorld - Friday, July 17, 2026
Home » Mpro inhibitors

Articles Tagged with ''Mpro inhibitors''

Infection

Gilead Sciences describes new Mpro inhibitors for SARS-CoV-2

Sep. 4, 2025
Gilead Sciences Inc. has identified 3C-like proteinase (3CLpro; Mpro; nsp5) (SARS-CoV-2; COVID-19 virus) inhibitors reported to be useful for the treatment of SARS-CoV-2 infection (COVID-19).
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Infection

New Mpro inhibitors revealed in Vir Biotechnology patent

April 10, 2025
Work at Vir Biotechnology Inc. has led to the identification of 3C-like proteinase (3CLpro; Mpro; nsp5) (SARS-CoV-2; COVID-19 virus) inhibitors reported to be useful for the treatment of SARS-CoV-2 infections (COVID-19).
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Infection

Shanghai Curegene Pharmaceutical divulges new Mpro inhibitors

Feb. 4, 2025
Shanghai Curegene Pharmaceutical Co. Ltd. has synthesized 3C-like proteinase (3CLpro; Mpro; nsp5) (SARS-CoV-2; COVID-19 virus) inhibitors reported to be useful for the treatment of SARS-CoV-2 infections (COVID-19).
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Infection

A*STAR reports new Mpro inhibitors

Dec. 5, 2024
The Agency for Science Technology & Research (A*STAR) Bioprocessing Technology Institute has patented 3C-like proteinase (3CLpro; Mpro; nsp5) (coronavirus) inhibitors.
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Infection

Westlake Pharmaceutical discloses new Mpro inhibitors

Nov. 8, 2024
Westlake Pharmaceutical (Hangzhou) Co. Ltd. has prepared and tested new 3C-like proteinase (3CLpro; Mpro; nsp5) inhibitors reported to be useful for the treatment of coronavirus acute respiratory syndrome.
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Infection

Tohoku University patents new 3CLpro inhibitors

Oct. 1, 2024
Tohoku University has disclosed 3C-like proteinase (3CLpro; Mpro; nsp5) (SARS-CoV-2; COVID-19 virus) inhibitors reported to be useful for the treatment of viral infections and inflammatory disorders.
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Creative rendition of SARS-CoV-2 virus particles.
Infection

Discovery of macrocyclic 3CLpro inhibitors with improved PK properties

Sep. 30, 2024
In work at Shanghai Curegene Pharmaceutical Co. Ltd., synthesis and optimization of a series of SARS-CoV-2 3CL protease (3CLpro, Mpro) inhibitors led to the identification of compounds [I], [II] and [III] as lead candidates suitable for further evaluation, based on their enzymatic IC50s (14, 12 and 8.6 nM, respectively), cellular EC50s (36, 26 and 52 nM, respectively) and human liver microsome (HLM) stability.
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Infection

Discovery and characterization of second-generation oral Mpro inhibitors

Sep. 20, 2024
Details on the work leading to the discovery of the second-generation SARS-CoV-2 main protease (Mpro) inhibitor PF-7817883 (ibuzatrelvir) were disclosed recently by Pfizer Inc. The drug is in phase II clinical development for the treatment of adult individuals with COVID-19 symptoms who are not hospitalized.
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Infection

Insilico Medicine divulges new Mpro inhibitors for SARS-CoV-2

Sep. 19, 2024
Insilico Medicine Inc. has synthesized 3C-like proteinase (3CLpro; Mpro; nsp5) (SARS-CoV-2; COVID-19 virus) inhibitors reported to be useful for the treatment of SARS-CoV-2 infection (COVID-19).
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Infection

Merck Sharp & Dohme synthesizes 3CLpro inhibitors for COVID-19

Aug. 6, 2024
Merck Sharp & Dohme LLC has disclosed 3C-like proteinase (3CLpro; Mpro; nsp5) (SARS-CoV-2; COVID-19 virus) inhibitors reported to be useful for the treatment of SARS-CoV-2 infection (COVID-19).
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