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

Authors :
Jennifer E. Vela
Adrian S. Ray
Sparacino Mark L
James M. Chen
Richard L. Mackman
David Y. Markevitch
Oleg V. Petrakovsky
Abraham C. Barron
David Sperandio
Ying Gao
Jay P. Parrish
Choung U. Kim
Sharon K. Lee
Tomas Cihlar
Genevieve Laflamme
Constantine G. Boojamra
Manoj C. Desai
Source :
Bioorganic & Medicinal Chemistry. 17:1739-1746
Publication Year :
2009
Publisher :
Elsevier BV, 2009.

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.

Details

ISSN :
09680896
Volume :
17
Database :
OpenAIRE
Journal :
Bioorganic & Medicinal Chemistry
Accession number :
edsair.doi.dedup.....01d31656d0e7ed412b7ae00ad6348354
Full Text :
https://doi.org/10.1016/j.bmc.2008.12.028