| Literature DB >> 33597253 |
Erol C Vatansever1, Kai S Yang1, Aleksandra K Drelich2, Kaci C Kratch1, Chia-Chuan Cho1, Kempaiah Rayavara Kempaiah2, Jason C Hsu2, Drake M Mellott3, Shiqing Xu1, Chien-Te K Tseng4,5, Wenshe Ray Liu6,3,7,8,9.
Abstract
Guided by a computational docking analysis, about 30 Food and Drug Administration/European Medicines Agency (FDA/EMA)-approved small-molecule medicines were characterized on their inhibition of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (Mp ro). Of these small molecules tested, six displayed a concentration that inhibits response by 50% (IC50) value below 100 μM in inhibiting Mp ro, and, importantly, three, that is, pimozide, ebastine, and bepridil, are basic molecules that potentiate dual functions by both raising endosomal pH to interfere with SARS-CoV-2 entry into the human cell host and inhibiting Mp ro in infected cells. A live virus-based modified microneutralization assay revealed that bepridil possesses significant anti-SARS-CoV-2 activity in both Vero E6 and A459/ACE2 cells in a dose-dependent manner with low micromolar effective concentration, 50% (EC50) values. Therefore, the current study urges serious considerations of using bepridil in COVID-19 clinical tests.Entities:
Keywords: COVID-19; SARS-CoV-2; bepridil; drug repurposing; main protease
Year: 2021 PMID: 33597253 DOI: 10.1073/pnas.2012201118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205