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Identifying novel inhibitors targeting Exportin-1 for the potential treatment of COVID-19

  • Tanuj Sharma,
  • Tanmoy Mondal,
  • Sajid Khan,
  • Marianela Patzi Churqui,
  • Kristina Nyström,
  • Ketan Thombare,
  • Mohammad Hassan Baig,
  • Jae-June Dong

摘要

The nuclear export protein 1 (XPO1) mediates the nucleocytoplasmic transport of proteins and ribonucleic acids (RNAs) and plays a prominent role in maintaining cellular homeostasis. XPO1 has emerged as a promising therapeutic approach to interfere with the lifecycle of many viruses. In our earlier study, we proved the inhibition of XPO1 as a therapeutic strategy for managing SARS-COV-2 and its variants. In this study, we have utilized pharmacophore-assisted computational methods to identify prominent XPO1 inhibitors. After several layers of screening, a few molecules were shortlisted for further experimental validation on the in vitro SARS-CoV-2 cell infection model. It was observed that these compounds reduced spike positivity, suggesting inhibition of SARS-COV-2 infection. The outcome of this study could be considered further for developing novel antiviral therapeutic strategies against SARS-CoV-2.