Synthesis and evaluation of 3′-azido-2′,3′-dideoxypurine nucleosides as inhibitors of human immunodeficiency virus

Samankaltaisia teoksia

• Anti-Human Immunodeficiency Virus Activity, Cross-Resistance, Cytotoxicity, and Intracellular Pharmacology of the 3′-Azido-2′,3′-Dideoxypurine Nucleosides
  Tekijä: Sluis-Cremer, Nicolas, et al.
  Julkaistu: (2009)
• Synthesis, antiviral activity, cytotoxicity and cellular pharmacology of l-3′-azido-2′,3′-dideoxypurine nucleosides
  Tekijä: Zhang, Hong-wang, et al.
  Julkaistu: (2011)
• The Base Component of 3′-Azido-2′,3′-Dideoxynucleosides Influences Resistance Mutations Selected in HIV-1 Reverse Transcriptase
  Tekijä: Meteer, Jeffrey D., et al.
  Julkaistu: (2011)
• Synthesis, antiviral activity, and stability of nucleoside analogs containing tricyclic bases
  Tekijä: Amblard, Franck, et al.
  Julkaistu: (2009)
• Substrate mimicry: HIV-1 reverse transcriptase recognizes 6-modified-3′-azido-2′,3′-dideoxyguanosine-5′-triphosphates as adenosine analogs
  Tekijä: Herman, Brian D., et al.
  Julkaistu: (2012)