ScholarWorks@경상국립대학교

초록

Despite the now infamous coronavirus disease outbreaks caused by severe acute respiratory syndrome coronavirus (SARS-CoV), this virus continues to be a threat to the global population. Although a huge research effort has targeted SARS-CoV, no report exists regarding natural small molecules targeting one of its key enzymes, papain-like protease (PLpro). In this study, nine flavonoids displaying SARS-CoV PLpro inhibitory activity were isolated from the root bark of Lespedeza bicolor. The compounds were identified as erythrabyssin II (1), lespebuergine G4 (2), 1-methoxyerythrabyssin II (3), bicolosin A (4), bicolosin B (5), bicolosin (6), xanthoangelol (7), (+/-)-lespeol (8), and parvisoflavanone (9). Most compounds (1-4 and 6-8) inhibited SARS-CoV PLpro activity in a dose-dependent manner, with their Kis ranging from 5.56 to 75.37 mu M. The structure-activity analysis of pterocarpans (1-6) showed that activity was enhanced by C1-OCH3, but it was reduced by C8-CH3. A mechanistic analysis revealed that all inhibitors were noncompetitive. Some of the key compounds isolated in this study are pterocarpans, which are abundantly present in the Leguminosae family. Overall, a rich source of SARS-CoV papain-like protease inhibitors was identified in this study.

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