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Discovery of S-217622, a Noncovalent Oral SARS-CoV-2 3CL Protease Inhibitor Clinical Candidate for Treating COVID-19.

Authors :
Unoh Y
Uehara S
Nakahara K
Nobori H
Yamatsu Y
Yamamoto S
Maruyama Y
Taoda Y
Kasamatsu K
Suto T
Kouki K
Nakahashi A
Kawashima S
Sanaki T
Toba S
Uemura K
Mizutare T
Ando S
Sasaki M
Orba Y
Sawa H
Sato A
Sato T
Kato T
Tachibana Y
Source :
Journal of medicinal chemistry [J Med Chem] 2022 May 12; Vol. 65 (9), pp. 6499-6512. Date of Electronic Publication: 2022 Mar 30.
Publication Year :
2022

Abstract

The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in millions of deaths and threatens public health and safety. Despite the rapid global spread of COVID-19 vaccines, effective oral antiviral drugs are urgently needed. Here, we describe the discovery of S-217622 , the first oral noncovalent, nonpeptidic SARS-CoV-2 3CL protease inhibitor clinical candidate. S-217622 was discovered via virtual screening followed by biological screening of an in-house compound library, and optimization of the hit compound using a structure-based drug design strategy. S-217622 exhibited antiviral activity in vitro against current outbreaking SARS-CoV-2 variants and showed favorable pharmacokinetic profiles in vivo for once-daily oral dosing. Furthermore, S-217622 dose-dependently inhibited intrapulmonary replication of SARS-CoV-2 in mice, indicating that this novel noncovalent inhibitor could be a potential oral agent for treating COVID-19.

Details

Language :
English
ISSN :
1520-4804
Volume :
65
Issue :
9
Database :
MEDLINE
Journal :
Journal of medicinal chemistry
Publication Type :
Academic Journal
Accession number :
35352927
Full Text :
https://doi.org/10.1021/acs.jmedchem.2c00117