Discovery of an L‐like Configuration for 3’‐Fluoro‐5’‐norcarbonucleoside Phosphonates as Potent Anti‐HIV Agents

Abstract: Recently, we reported the racemic synthesis of 3’‐fluoro‐5’‐norcarbocyclic nucleoside phosphonates bearing adenine as the heterocyclic base. For this study, to evaluate the antiviral activity of each enantiomer, we synthesized both enantiomers, as well as their corresponding bis (POM) prodrugs. Anti‐HIV‐1 evaluation against the LAI strain and clinically NRTI‐resistant HIV‐1 strains are presented. The activities against these different strains show that the activities of bis (POM) prodrug (−)‐9 are equivalent or even superior to those of (R)‐PMPA.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Discovery of an L‐like Configuration for 3’‐Fluoro‐5’‐norcarbonucleoside Phosphonates as Potent Anti‐HIV Agents ; day:15 ; month:09 ; year:2022 ; extent:1
ChemMedChem ; (15.09.2022) (gesamt 1)

Creator
Geant, Pierre‐Yves
Kaci, Malika
Uttaro, Jean‐Pierre
Périgaud, Christian
Mathé, Christophe

DOI
10.1002/cmdc.202200377
URN
urn:nbn:de:101:1-2022091615110164121114
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.0009, 8:29 AM CET

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Associated

  • Geant, Pierre‐Yves
  • Kaci, Malika
  • Uttaro, Jean‐Pierre
  • Périgaud, Christian
  • Mathé, Christophe

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