1. Academic Validation
  2. 4-Hydroxychalcone Inhibits Human Coronavirus HCoV-OC43 by Targeting EGFR/AKT/ERK1/2 Signaling Pathway

4-Hydroxychalcone Inhibits Human Coronavirus HCoV-OC43 by Targeting EGFR/AKT/ERK1/2 Signaling Pathway

  • Viruses. 2025 Jul 23;17(8):1028. doi: 10.3390/v17081028.
Yuanyuan Huang 1 2 Jieyu Li 1 2 Qiting Luo 2 Yuexiang Dai 1 Xinyi Luo 2 Jiapeng Xu 2 Wei Ye 2 Xinrui Zhou 2 Jiayi Diao 2 Zhe Ren 3 Ge Liu 2 Zhendan He 2 Zhiping Wang 1 Yifei Wang 1 3 Qinchang Zhu 2
Affiliations

Affiliations

  • 1 School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China.
  • 2 College of Pharmacy, Shenzhen Technology University, Shenzhen 518118, China.
  • 3 Guangdong Province Key Laboratory of Bioengineering Medicine, Key Laboratory of Innovative Technology Research on Natural Products and Cosmetics Raw Materials, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Abstract

Human coronaviruses are a group of viruses that continue to threaten human health. In this study, we investigated the Antiviral activity of 4-hydroxychalcone (4HCH), a chalcone derivative, against human coronavirus HCoV-OC43. We found that 4HCH significantly inhibited the cytopathic effect, reduced viral protein and RNA levels in infected cells, and increased the survival rate of HCoV-OC43-infected suckling mice. Mechanistically, 4HCH targets the early stages of viral Infection by binding to the epidermal growth factor receptor (EGFR) and inhibiting the EGFR/Akt/ERK1/2 signaling pathway, thereby suppressing viral replication. Additionally, 4HCH significantly reduced the production of pro-inflammatory cytokines and chemokines in both HCoV-OC43-infected RD cells and a suckling mouse model. Our findings demonstrate that 4HCH exhibits potent Antiviral activity both in vitro and in vivo, suggesting its potential as a therapeutic agent against human coronaviruses. This study highlights EGFR as a promising host target for Antiviral drug development and positions 4HCH as a candidate for further investigation in the treatment of coronavirus infections.

Keywords

4-hydroxychalcone; EGFR; EGFR/AKT/ERK1/2 signaling pathway; antiviral activity; flavonoids; human coronavirus.

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