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Updated: Jun 27, 2026

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
Published on: May 9, 2025
Design and synthesis of vidarabine prodrugs as antiviral agents
Wei Shen1, Jae-Seung Kim, Phillip E Kish
1TSRL Inc., 540 Avis Drive Suite A, Ann Arbor, MI 48108, USA. wshen@tsrlinc.com
Abstract:
5'-O-D- and L-amino acid derivatives and 5'-O-(D- and L-amino acid methyl ester phosphoramidate) derivatives of vidarabine (ara-A) were synthesized as vidarabine prodrugs. Some compounds were equi- or more potent in vitro than vidarabine against two pox viruses and their uptake by cultured cells was improved compared to the parent drug.
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