Synthesis and biological activity of 4'-C-hydroxymethyl-2'-fluoro-D-arabinofuranosylpurine nucleosides
A T Shortnacy-Fowler1, K N Tiwari, J A Montgomery
1Southern Research Institute, P.O. Box 55305, Birmingham, Alabama 35255-5305, USA.
Abstract:
A series of 4'-C-hydroxymethyl-2'-fluoro-D-arabinofuranosylpurine nucleosides was prepared and evaluated for cytotoxicity in human tumor cell lines. A convenient synthesis of the carbohydrate precursor 4-C-hydroxymethyl-3,5-di-O-benzoyl-2-fluoro-alpha-D-arabinofuranosyl bromide (13) was developed. Coupling of 13 with the sodium salt of 2,6-dichloropurine led to five target purine nucleosides.
More Related Videos
10:24NMR-Based Activity Assays for Determining Compound Inhibition, IC50 Values, Artifactual Activity, and Whole-Cell Activity of Nucleoside Ribohydrolases
Published on: June 30, 2019
08:17A High-Throughput Enzyme-Coupled Activity Assay to Probe Small Molecule Interaction with the dNTPase SAMHD1
Published on: April 16, 2021
Related Concept Videos
Antiviral Nucleoside Inhibitors
Biosynthesis of Nucleic Acids
DNA Base Pairing
Inhibitors of Bacterial DNA Synthesis
Inhibitors of Viral Protein Synthesis
Biosynthesis of Polysaccharides
