Synthesis of nucleoside phosphate and phosphonate prodrugs

U Pradere, EC Garnier-Amblard, SJ Coats… - Chemical …, 2014 - ACS Publications
For many decades, the design of new nucleoside analogs as potential therapeutic agents
focused on both sugar and nucleobase modifications. These nucleoside analogs rely on …

Recent Advances in the Synthesis of Acyclic Nucleosides and Their Therapeutic Applications

S Kumar, A Arora, R Chaudhary, R Kumar… - Topics in Current …, 2024 - Springer
DNA is commonly known as the “molecule of life” because it holds the genetic instructions
for all living organisms on Earth. The utilization of modified nucleosides holds the potential …

Synthesis and evaluation of prodrugs of α-carboxy nucleoside phosphonates

A Ford, ND Mullins, J Balzarini… - The Journal of Organic …, 2022 - ACS Publications
A range of lipophilic prodrugs of α-carboxy nucleoside phosphonates, potent inhibitors of
HIV-1 reverse transcriptase without requiring prior phosphorylation, were synthesized to …

[HTML][HTML] Synthesis of LAVR-289, a new [(Z)-3-(acetoxymethyl)-4-(2, 4-diaminopyrimidin-6-yl) oxy-but-2-enyl] phosphonic acid prodrug with pronounced antiviral activity …

M Bessières, V Roy, T Abuduani, P Favetta… - European Journal of …, 2024 - Elsevier
New acyclic pyrimidine nucleoside phosphonate prodrugs with a 4-(2, 4-diaminopyrimidin-6-
yl) oxy-but-2-enyl] phosphonic acid skeleton (O-DAPy nucleobase) were prepared through a …

Synthesis and broad spectrum antiviral evaluation of bis (POM) prodrugs of novel acyclic nucleosides

M Hamada, V Roy, TR McBrayer, T Whitaker… - European Journal of …, 2013 - Elsevier
A series of seventeen hitherto unknown ANP analogs bearing the (E)-but-2-enyl aliphatic
side chain and modified heterocyclic base such as cytosine and 5-fluorocytosine, 2 …

Highly convergent synthesis and antiviral activity of (E)-but-2-enyl nucleoside phosphonoamidates

M Bessières, V Hervin, V Roy, A Chartier… - European Journal of …, 2018 - Elsevier
Several hitherto unknown (E)-but-2-enyl nucleoside phosphonoamidate analogs (ANPs)
were prepared directed with nitrogen reagents by cross-metathesis in water-under …

Fluorophosphonylated nucleoside derivatives as new series of thymidine phosphorylase multisubstrate inhibitors

SA Diab, C De Schutter, M Muzard… - Journal of medicinal …, 2012 - ACS Publications
The synthesis of new class of potential TPase inhibitors containing a
difluoromethylphosphonate function as phosphate mimic is reported. This new series was …

[HTML][HTML] Lyotropic liquid crystal emulsions of LAVR-289: Influence of internal mesophase structure on cytotoxicity and in-vitro antiviral activity

M Brouillard, T Mathieu, S Guillot, F Méducin… - International Journal of …, 2024 - Elsevier
Emerging and reemerging viruses pose significant public health threats, underscoring the
urgent need for new antiviral drugs. Recently, a novel family of antiviral acyclic nucleoside …

Synthesis and antiviral evaluation of bis (POM) prodrugs of (E)-[4′-phosphono-but-2′-en-1′-yl] purine nucleosides

U Pradère, V Roy, A Montagu, O Sari… - European journal of …, 2012 - Elsevier
Seventeen hitherto unknown bis (POM) prodrugs of novel (E)-[4′-phosphono-but-2′-en-
1′-yl] purine nucleosides were prepared in a straight approach and at good yields. Those …

Synthesis and Antiviral Evaluation of (1,4-Disubstituted-1,2,3-Triazol)-(E)-2-Methyl-but-2-Enyl Nucleoside Phosphonate Prodrugs

T Abuduaini, V Roy, J Marlet, C Gaudy-Graffin, D Brand… - Molecules, 2021 - mdpi.com
A series of hitherto unknown (1, 4-disubstituted-1, 2, 3-triazol)-(E)-2-methyl-but-2-enyl
nucleosides phosphonate prodrugs bearing 4-substituted-1, 2, 3-triazoles were prepared in …