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Design, synthesis, and anti-HIV activity of 4′-modified carbocyclic nucleoside phosphonate reverse transcriptase inhibitors
- 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.
- Subjects :
- Models, Molecular
Anti-HIV Agents
Metabolite
Clinical Biochemistry
Organophosphonates
Pharmaceutical Science
Biochemistry
Structure-Activity Relationship
chemistry.chemical_compound
Cell Line, Tumor
Drug Discovery
Humans
Structure–activity relationship
Prodrugs
Nucleotide
Molecular Biology
chemistry.chemical_classification
Molecular Structure
Organic Chemistry
Nucleosides
Prodrug
Phosphonate
HIV Reverse Transcriptase
In vitro
Reverse transcriptase
chemistry
Drug Design
Reverse Transcriptase Inhibitors
Molecular Medicine
Nucleoside
Subjects
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