Synthesis of nucleoside phosphate and phosphonate prodrugs

U Pradere, EC Garnier-Amblard, SJ Coats… - Chemical …, 2014 - ACS Publications
For many decades, the design of new nucleoside analogs as potential therapeutic agents
focused on both sugar and nucleobase modifications. These nucleoside analogs rely on …

Nucleoside, nucleotide, and non-nucleoside inhibitors of hepatitis C virus NS5B RNA-dependent RNA-polymerase

MJ Sofia, W Chang, PA Furman… - Journal of medicinal …, 2012 - ACS Publications
Hepatitis C virus (HCV) infection is a global health problem that impacts approximately 180
million individuals. Of those initially infected with HCV approximately 80% will progress to …

Prodrugs of phosphonates and phosphates: crossing the membrane barrier

AJ Wiemer, DF Wiemer - … Chemistry I: Asymmetric Synthesis and Bioactive …, 2015 - Springer
A substantial portion of metabolism involves transformation of phosphate esters, including
pathways leading to nucleotides and oligonucleotides, carbohydrates, isoprenoids and …

Phosphoramidates and phosphonamidates (ProTides) with antiviral activity

M Slusarczyk, M Serpi… - Antiviral Chemistry and …, 2018 - journals.sagepub.com
Following the first report on the nucleoside phosphoramidate (ProTide) prodrug approach in
1990 by Chris McGuigan, the extensive investigation of ProTide technology has begun in …

Cu from dissolution of CuO nanoparticles signals changes in root morphology

J Adams, M Wright, H Wagner, J Valiente, D Britt… - Plant physiology and …, 2017 - Elsevier
Abstract Utilization of CuO nanoparticles (NPs) in agriculture, as fertilizers or pesticides,
requires understanding of their impact on plant metabolism. Inhibition of root elongation by …

Role of a “Magic” Methyl: 2′-Deoxy-2′-α-F-2′-β-C-methyl Pyrimidine Nucleotides Modulate RNA Interference Activity through Synergy with 5′-Phosphate Mimics …

DC Guenther, S Mori, S Matsuda… - Journal of the …, 2022 - ACS Publications
Although 2′-deoxy-2′-α-F-2′-β-C-methyl (2′-F/Me) uridine nucleoside derivatives are a
successful class of antiviral drugs, this modification had not been studied in …

Preclinical evaluation of AT-527, a novel guanosine nucleotide prodrug with potent, pan-genotypic activity against hepatitis C virus

SS Good, A Moussa, XJ Zhou, K Pietropaolo… - PLoS …, 2020 - journals.plos.org
Despite the availability of highly effective direct-acting antiviral (DAA) regimens for the
treatment of hepatitis C virus (HCV) infections, sustained viral response (SVR) rates remain …

2′-Fluorinated nucleoside chemistry for new drug discovery: achievements and prospects

Y Meng, N Sun, L Liang, B Yu… - National Science …, 2024 - academic.oup.com
Fluorinated nucleosides are an important class of modified nucleosides that have
demonstrated therapeutic potential for treating various human diseases, especially viral …

Nucleotide prodrugs for HCV therapy

MJ Sofia - Antiviral Chemistry and Chemotherapy, 2011 - journals.sagepub.com
HCV infection is a significant worldwide health problem and is a major cause of
hepatocellular carcinoma. The current standard of care, interferon and ribavirin, is only …

[HTML][HTML] Recent advances in synthetic approaches for medicinal chemistry of C-nucleosides

K Temburnikar… - Beilstein Journal of Organic …, 2018 - beilstein-journals.org
C-nucleosides have intrigued biologists and medicinal chemists since their discovery in
1950's. In that regard, C-nucleosides and their synthetic analogues have resulted in …