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  • 作者: Fang Qiongqiong Wang Dayan
  • 学科: 医药卫生 >
  • 创建时间:2020-08-10
  • 出处:《生物安全与健康 (英文)》 2020年第02期
  • 机构:National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China; WHO Collaborating Center for Reference and Research on Influenza, Beijing 102206, China; Key Laboratory for Medical Virology, National Health Commission, Beijing 102206, China
  • 简介:AbstractAnti-influenza drugs are one of the most critical pathways for control of influenza virus infection. Drugs that have been developed or are developing may function via different mechanisms, and so far, inhibitors of influenza virus polymerase are among the most promising types of drugs. Favipiravir and Baloxavir, also named T-705 and Xofluza respectively, have been approved for influenza treatment in Japan and the United States. Favipiravir effectively and selectively inhibits the RNA-dependent RNA polymerase (RdRp) of RNA viruses while Baloxavir specifically targets the cap-dependent endonuclease PA of influenza viruses. These two drugs have been suggested as the first candidate drugs for influenza infection treatment, especially for strains resistant to other anti-influenza drugs. This review will focus on the pharmaceutical mechanisms and anti-influenza activity of these two drugs.

  • 标签: Favipiravir Baloxavir Influenza virus Anti-influenza drug Drug target