Literature DB >> 19179082

Design, synthesis, and anti-HIV activity of 4'-modified carbocyclic nucleoside phosphonate reverse transcriptase inhibitors.

Constantine G Boojamra1, Jay P Parrish, David Sperandio, Ying Gao, Oleg V Petrakovsky, Sharon K Lee, David Y Markevitch, Jennifer E Vela, Genevieve Laflamme, James M Chen, Adrian S Ray, Abraham C Barron, Mark L Sparacino, Manoj C Desai, Choung U Kim, Tomas Cihlar, Richard L Mackman.   

Abstract

A diphosphate of a novel cyclopentyl based nucleoside phosphonate with potent inhibition of HIV reverse transcriptase (RT) (20, IC(50)=0.13 microM) has been discovered. In cell culture the parent phosphonate diacid 9 demonstrated antiviral activity EC(50)=16 microM, within two-fold of GS-9148, a prodrug of which is currently under clinical investigation, and within 5-fold of tenofovir (PMPA). In vitro cellular metabolism studies using 9 confirmed that the active diphosphate metabolite is produced albeit at a lower efficiency relative to GS-9148.

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Year:  2008        PMID: 19179082     DOI: 10.1016/j.bmc.2008.12.028

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  3 in total

1.  Development of modified nucleosides that have supremely high anti-HIV activity and low toxicity and prevent the emergence of resistant HIV mutants.

Authors:  Hiroshi Ohrui
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2011       Impact factor: 3.493

2.  Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues.

Authors:  Bemba Sidi Mohamed; Christian Périgaud; Christophe Mathé
Journal:  Beilstein J Org Chem       Date:  2017-02-09       Impact factor: 2.883

Review 3.  Adenine: an important drug scaffold for the design of antiviral agents.

Authors:  Changyuan Wang; Zhendong Song; Haiqing Yu; Kexin Liu; Xiaodong Ma
Journal:  Acta Pharm Sin B       Date:  2015-09-02       Impact factor: 11.413

  3 in total

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