Synthesis and anti-HIV activities of bis-(cycloSaligenyl) pronucleotides derivatives of 3′-fluoro-3′-deoxythymidine and 3′-azido-3′-deoxythymidine

Podobne knjige/članki

• Synthesis of Nucleoside Mono-, Di-, and Triphosphoramidates from Solid-Phase CycloSaligenyl Phosphitylating Reagents
  od: Ahmadibeni, Yousef, et al.
  Izdano: (2009)
• Synthesis of β-triphosphotriester pronucleotides
  od: Beni, Yousef, et al.
  Izdano: (2015)
• N-Myristoylglutamic Acid Derivative of 3′-Fluoro-3′-Deoxythymidine as an Organogel
  od: Chhikara, Bhupender S., et al.
  Izdano: (2012)
• Radiolabeled cycloSaligenyl Monophosphates of 5-Iodo-2′-deoxyuridine, 5-Iodo-3′-fluoro-2′, 3′-dideoxyuridine, and 3′-Fluorothymidine for Molecular Radiotherapy of Cancer: Synthesis and Biological Evaluation
  od: Kortylewicz, Zbigniew P., et al.
  Izdano: (2012)
• Comparisons of anti-human immunodeficiency virus activities, cellular transport, and plasma and intracellular pharmacokinetics of 3'-fluoro-3'-deoxythymidine and 3'-azido-3'-deoxythymidine.
  od: Kong, X B, et al.
  Izdano: (1992)