2. Academic Validation
  3. Identification of SARS-CoV-2 entry inhibitors among already approved drugs

Identification of SARS-CoV-2 entry inhibitors among already approved drugs

  • Acta Pharmacol Sin. 2021 Aug;42(8):1347-1353. doi: 10.1038/s41401-020-00556-6.
Li Yang  # 1,  Rong-Juan Pei  # 2,  Heng Li  # 1 3,  Xin-Na Ma 4,  Yu Zhou 1,  Feng-Hua Zhu 1,  Pei-Lan He 1,  Wei Tang 1,  Ye-Cheng Zhang 2,  Jin Xiong 2,  Shu-Qi Xiao 2,  Xian-Kun Tong 5,  Bo Zhang 6,  Jian-Ping Zuo 7 8 9
Affiliations

Affiliations

  • 1 Laboratory of Immunopharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
  • 2 Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, 430071, China.
  • 3 University of Chinese Academy of Sciences, Beijing, 100049, China.
  • 4 Laboratory of Immunology and Virology, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
  • 5 Laboratory of Immunopharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. [email protected].
  • 6 Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, 430071, China. [email protected].
  • 7 Laboratory of Immunopharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. [email protected].
  • 8 University of Chinese Academy of Sciences, Beijing, 100049, China. [email protected].
  • 9 Laboratory of Immunology and Virology, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China. [email protected].
  • # Contributed equally.
PMID: 33116249 DOI: 10.1038/s41401-020-00556-6
Abstract

To discover effective drugs for COVID-19 treatment amongst already clinically approved drugs, we developed a high throughput screening assay for SARS-CoV-2 virus entry inhibitors using SARS2-S pseudotyped virus. An approved drug library of 1800 small molecular drugs was screened for SARS2 entry inhibitors and 15 active drugs were identified as specific SARS2-S pseudovirus entry inhibitors. Antiviral tests using native SARS-CoV-2 virus in Vero E6 cells confirmed that 7 of these drugs (clemastine, amiodarone, trimeprazine, bosutinib, toremifene, flupenthixol, and azelastine) significantly inhibited SARS2 replication, reducing supernatant viral RNA load with a promising level of activity. Three of the drugs were classified as Histamine Receptor antagonists with clemastine showing the strongest anti-SARS2 activity (EC50 = 0.95 ± 0.83 µM). Our work suggests that these 7 drugs could enter into further in vivo studies and clinical investigations for COVID-19 treatment.

Keywords

COVID-19; SARS-CoV-2; approved drug library; clemastine; high throughput screening assay; histamine receptor antagonists; virus entry inhibitors.

Figures
Products