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  • Abstract Nucleoside analogues that have 6-chloropurine as the nucleobase were synthesized and evaluated for anti-SARS-CoV activity by plaque reduction and yield reduction assays in order to develop novel anti-SARS-CoV agents. Among these analogues, two compounds, namely, 1 and 11, exhibited promising anti-SARS-CoV activity that was comparable to those of mizoribine and ribavirin, which are known anti-SARS-CoV agents. Moreover, we observed several SAR trends such as the antiviral effects of the 6-chloropurine moiety, unprotected 5′-hydroxyl group and benzoylated 5′-hydroxyl group.
Subject
  • Alcohols
  • Antivirals
  • Anti-hepatitis C agents
  • Functional groups
  • Immunosuppressants
  • Hydroxides
  • Sarbecovirus
  • Chiroptera-borne diseases
  • Infraspecific virus taxa
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