SARS-CoV-2 Papain-Like Protease Inhibitors Based on Naphthalen-1-ylethanamine and Halogenated Benzene Moieties

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is the causative virus of COVID-19, remains a worldwide health threat. SARS-CoV-2 possesses two types of proteases: a main protease (M<sup>pro</sup>, 3C-like) and a papain-like protease (PL<sup>pro</sup>). These proteases cleave two translated nonstructural proteins, pp1a and pp1ab, into viral functional proteins. In the present study, we developed new inhibitors targeting the PL<sup>pro</sup> of SARS-CoV-2 based on GRL-0048 (<b>2</b>) as a lead compound. Structure-activity relationship (SAR) researches on GRL-0048 (<b>2</b>) led to the finding of compound <b>9r</b>, which showed significantly enhanced inhibitory activity against PL<sup>pro</sup>. This enhancement was accomplished by the introduction of a halogenated aromatic carbonyl moiety into the parent structure of GRL-0048 (<b>2</b>).

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Publication Details

Journal
ACS Omega
Published
2025-10-02
DOI
https://doi.org/10.1021/acsomega.5c05856
Citations
1
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.94
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article

SARS-CoV-2 Papain-Like Protease Inhibitors Based on Naphthalen-1-ylethanamine and Halogenated Benzene Moieties

Hiroaki Mitsuya, Takuya Kobayakawa, Kouki Shinohara, Yuki Takamatsu et al.
1 citations
ACS Omega
Synthesis and biological activity
0.94
article

SARS-CoV-2 Papain-Like Protease Inhibitors Based on Naphthalen-1-ylethanamine and Halogenated Benzene Moieties

Hiroaki Mitsuya, Takuya Kobayakawa, Kouki Shinohara, Yuki Takamatsu, Hirokazu Tamamura, Kohei Tsuji
article en
1 citations

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is the causative virus of COVID-19, remains a worldwide health threat. SARS-CoV-2 possesses two types of proteases: a main protease (M<sup>pro</sup>, 3C-like) and a papain-like protease (PL<sup>pro</sup>). These proteases cleave two translated nonstructural proteins, pp1a and pp1ab, into viral functional proteins. In the present study, we developed new inhibitors targeting the PL<sup>pro</sup> of SARS-CoV-2 based on GRL-0048 (<b>2</b>) as a lead compound. Structure-activity relationship (SAR) researches on GRL-0048 (<b>2</b>) led to the finding of compound <b>9r</b>, which showed significantly enhanced inhibitory activity against PL<sup>pro</sup>. This enhancement was accomplished by the introduction of a halogenated aromatic carbonyl moiety into the parent structure of GRL-0048 (<b>2</b>).

ACS OmegaVol. 10(40)
Tokyo Medical and Dental University (JP), National Institutes of Health (US), Shanghai Institute for Science of Science (CN), National Center for Global Health and Medicine (JP), Kumamoto University Hospital (JP), National Cancer Institute (MY), National Cancer Institute (US), Bioengineering Center (RU), Ekaterinburg Research Institute of Viral Infections (RU), Institute of Science Tokyo (JP)
Openalex Percentile: Top 21%
Synthesis and biological activity
0.94
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