Lipophilic halogenated congeners of 2',3'-dideoxypurine nucleosides active against human immunodeficiency virus in vitro.

Lignende værker

• Pharmacokinetics of dideoxypurine nucleoside analogs in plasma and cerebrospinal fluid of rhesus monkeys.
  af: Hawkins, M E, et al.
  Udgivet: (1995)
• Adenallene and cytallene: acyclic-nucleoside analogues that inhibit replication and cytopathic effect of human immunodeficiency virus in vitro.
  af: Hayashi, S, et al.
  Udgivet: (1988)
• Synthesis and evaluation of 3′-azido-2′,3′-dideoxypurine nucleosides as inhibitors of human immunodeficiency virus
  af: Hong-wang, Zhang, et al.
  Udgivet: (2009)
• Changes in drug sensitivity of human immunodeficiency virus type 1 during therapy with azidothymidine, dideoxycytidine, and dideoxyinosine: an in vitro comparative study.
  af: Shirasaka, T, et al.
  Udgivet: (1993)
• Anti-Human Immunodeficiency Virus Activity, Cross-Resistance, Cytotoxicity, and Intracellular Pharmacology of the 3′-Azido-2′,3′-Dideoxypurine Nucleosides
  af: Sluis-Cremer, Nicolas, et al.
  Udgivet: (2009)