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Merck
CN

Novel nucleosides as potent influenza viral inhibitors.

Bioorganic & medicinal chemistry (2010-08-03)
Manohar Sharma Vedula, Sreenu Jennepalli, Ratnakar Aryasomayajula, Subhash Reddy Rondla, Madanmohan Reddy Musku, Rathnakar Reddy Kura, Parthasaradhi Reddy Bandi
ABSTRACT

Influenza virus infection constitutes a significant health problem in need of more effective therapies. We have recently identified ((2R,3S,4R,5R)-3-acetoxy-5-(4-benzamido-2-oxopyrimidin-1(2H)-yl)-4-fluoro-3,4-dimethyl-tetrahydrofuran-2-yl) methyl benzoate (18c) as a potent influenza virus inhibitor. We now here report the synthesis and evaluation of a series of C-3' modified ribose nucleosides. These novel compounds were prepared, primarily by taking known ((2R,3R,4R)-3-benzoyloxy-4-fluoro-4-methyl-5-oxo-tetrahydrofuran-2-yl)methyl benzoate (1) and converting it in to C-3 keto sugar (7), reacting C-3 keto group with methyl magnesium bromide, followed by coupling these sugars with purine and pyrimidine bases. Anti influenza viral activity was determined by screening against both A and B viral strains.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Thymine, ≥99%
Sigma-Aldrich
Fluorouracil, meets USP testing specifications
Sigma-Aldrich
5-Fluorouracil, ≥99% (HPLC), powder
Sigma-Aldrich
Thymine, BioReagent, suitable for cell culture
Sigma-Aldrich
Uracil, ≥99.0%
Sigma-Aldrich
Uracil, BioReagent, suitable for cell culture