Ethacridine inhibits SARS-CoV-2 by inactivating viral particles in cellular models

依沙吖啶通过灭活细胞模型中的病毒颗粒来抑制 SARS-CoV-2

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作者:Xiaoquan Li, Peter Lidsky, Yinghong Xiao, Chien-Ting Wu, Miguel GarciaKnight, Junjiao Yang, Tsuguhisa Nakayama, Jayakar V Nayak, Peter K Jackson, Raul Andino, Xiaokun Shu

Abstract

SARS-CoV-2 is the coronavirus that causes the respiratory disease COVID-19, which is now the third-leading cause of death in the United States. The FDA has recently approved remdesivir, an inhibitor of SARS-CoV-2 replication, to treat COVID-19, though recent data from the WHO shows little to no benefit with use of this anti-viral agent. Here we report the discovery of ethacridine, a safe antiseptic use in humans, as a potent drug for use against SARS-CoV-2 (EC50 ~ 0.08 μM). Ethacridine was identified via high-throughput screening of an FDA-approved drug library in living cells using a fluorescent assay. Interestingly, the main mode of action of ethacridine is through inactivation of viral particles, preventing their binding to the host cells. Indeed, ethacridine is effective in various cell types, including primary human nasal epithelial cells. Taken together, these data identify a promising, potent, and new use of the old drug possessing a distinct mode of action for inhibiting SARS-CoV-2.

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