Nucleic Acids as a Nature-Inspired Scaffold for Macromolecular Prodrugs of Nucleoside Analogues

Franziska Krüger, Vipin Kumar, Pere Monge, Carina Conzelmann, Nikaïa Smith, Kurt V. Gothelf, Martin Tolstrup, Jan Münch*, Alexander N. Zelikin

*Corresponding author for this work

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

Abstract

Macromolecular prodrugs (MP) built on the natural phosphodiester and deoxyribose backbone are developed using marketed antiviral nucleoside analogues. These MP are synthesized using automated synthesis, have defined molecular composition, and have a natural mechanism for drug release. These unique attributes, coupled to the efficient cell entry and potent antiviral effects, position the prodrugs scaffolded on nucleic acids favorably for translational studies.

Original languageEnglish
Article number1802095
JournalAdvanced Science
Volume6
Issue6
DOIs
Publication statusPublished - 2019

Keywords

  • antivirals
  • herpes simplex virus
  • nucleic acids
  • nucleoside analogues
  • prodrugs

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