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Synthesis and Antiviral Evaluation of (1,4-Disubstituted-1,2,3-Triazol)-(E)-2-Methyl-but-2-Enyl Nucleoside Phosphonate Prodrugs
Authors:Tuniyazi Abuduaini  Vincent Roy  Julien Marlet  Catherine Gaudy-Graffin  Denys Brand  Ccile Baronti  Franck Touret  Bruno Coutard  Tamara R McBrayer  Raymond F Schinazi  Luigi A Agrofoglio
Abstract: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 a straight approach through an olefin acyclic cross metathesis as the key synthetic step. All novel compounds were evaluated for their antiviral activities against HBV, HIV and SARS-CoV-2. Among these molecules, only compound 15j, a hexadecyloxypropyl (HDP)/(isopropyloxycarbonyl-oxymethyl)-ester (POC) prodrug, showed activity against HBV in Huh7 cell cultures with 62% inhibition at 10 μM, without significant cytotoxicity (IC50 = 66.4 μM in HepG2 cells, IC50 = 43.1 μM in HepG2 cells) at 10 μM.
Keywords:nucleosides  olefin cross metathesis  ultrasound  copper-catalyzed azide-alkyne cycloaddition (CuAAC)  antiviral properties  HBV  HIV  SARS-CoV-2
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