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Novel Pan-Coronavirus 3CL Protease Inhibitor MK-7845: Biological and Pharmacological Profiling.

Authors :
Alvarez, Nadine
Adam, Gregory C.
Howe, John A.
Sharma, Vijeta
Zimmerman, Matthew D.
Dolgov, Enriko
Rasheed, Risha
Nizar, Fatima
Sahay, Khushboo
Nelson, Andrew M.
Park, Steven
Zhou, Xiaoyan
Burlein, Christine
Fay, John F.
Iwamoto, Daniel V.
Bahnck-Teets, Carolyn M.
Getty, Krista L.
Lin Goh, Shih
Salhab, Imad
Smith, Keith
Source :
Viruses (1999-4915). Jul2024, Vol. 16 Issue 7, p1158. 22p.
Publication Year :
2024

Abstract

Severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) continues to be a global threat due to its ability to evolve and generate new subvariants, leading to new waves of infection. Additionally, other coronaviruses like Middle East respiratory syndrome coronavirus (MERS-CoV, formerly known as hCoV-EMC), which first emerged in 2012, persist and continue to present a threat of severe illness to humans. The continued identification of novel coronaviruses, coupled with the potential for genetic recombination between different strains, raises the possibility of new coronavirus clades of global concern emerging. As a result, there is a pressing need for pan-CoV therapeutic drugs and vaccines. After the extensive optimization of an HCV protease inhibitor screening hit, a novel 3CLPro inhibitor (MK-7845) was discovered and subsequently profiled. MK-7845 exhibited nanomolar in vitro potency with broad spectrum activity against a panel of clinical SARS-CoV-2 subvariants and MERS-CoV. Furthermore, when administered orally, MK-7845 demonstrated a notable reduction in viral burdens by >6 log orders in the lungs of transgenic mice infected with SARS-CoV-2 (K18-hACE2 mice) and MERS-CoV (K18-hDDP4 mice). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19994915
Volume :
16
Issue :
7
Database :
Academic Search Index
Journal :
Viruses (1999-4915)
Publication Type :
Academic Journal
Accession number :
178697788
Full Text :
https://doi.org/10.3390/v16071158