2',3'-dideoxy-beta-L-5-fluorocytidine inhibits duck hepatitis B virus reverse transcription and suppresses viral DNA synthesis in hepatocytes, both in vitro and in vivo.

Ítems similars

• Characterization of the Antiviral Effect of 2′,3′-Dideoxy-2′, 3′-Didehydro-β-l-5-Fluorocytidine in the Duck Hepatitis B Virus Infection Model
  per: Le Guerhier, Franck, et al.
  Publicat: (2000)
• Antiviral Activity of β-l-2′,3′-Dideoxy-2′,3′-Didehydro-5-Fluorocytidine in Woodchucks Chronically Infected with Woodchuck Hepatitis Virus
  per: Le Guerhier, F., et al.
  Publicat: (2001)
• n-Butyrate, a cell cycle blocker, inhibits early amplification of duck hepatitis B virus covalently closed circular DNA after in vitro infection of duck hepatocytes.
  per: Turin, F, et al.
  Publicat: (1996)
• Inhibitory Effect of Adefovir on Viral DNA Synthesis and Covalently Closed Circular DNA Formation in Duck Hepatitis B Virus-Infected Hepatocytes In Vivo and In Vitro
  per: Delmas, Julien, et al.
  Publicat: (2002)
• Selective inhibition of the duck hepatitis B virus by a new class of tetraazamacrocycles.
  per: Hantz, O, et al.
  Publicat: (1997)