Remdesivir: a review of its discovery and development leading to emergency use authorization for treatment of COVID-19

RT Eastman, JS Roth, KR Brimacombe… - ACS central …, 2020 - ACS Publications
The global pandemic of SARS-CoV-2, the causative viral pathogen of COVID-19, has driven
the biomedical community to action—to uncover and develop antiviral interventions. One …

[HTML][HTML] 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 …

The ProTide Prodrug Technology: From the Concept to the Clinic: Miniperspective

Y Mehellou, HS Rattan, J Balzarini - Journal of medicinal …, 2017 - ACS Publications
The ProTide technology is a prodrug approach developed for the efficient intracellular
delivery of nucleoside analogue monophosphates and monophosphonates. In this …

Discovery of a β-d-2′-Deoxy-2′-α-fluoro-2′-β-C-methyluridine Nucleotide Prodrug (PSI-7977) for the Treatment of Hepatitis C Virus

MJ Sofia, D Bao, W Chang, J Du… - Journal of medicinal …, 2010 - ACS Publications
Hepatitis C virus (HCV) is a global health problem requiring novel approaches for effective
treatment of this disease. The HCV NS5B polymerase has been demonstrated to be a viable …

Strategies in the design of antiviral drugs

E De Clercq - Nature Reviews drug discovery, 2002 - nature.com
A decade ago, just five drugs were licensed for the treatment of viral infections. Since then,
greater understanding of viral life cycles, prompted in particular by the need to combat …

Prodrugs of phosphates and phosphonates

SJ Hecker, MD Erion - Journal of medicinal chemistry, 2008 - ACS Publications
Phosphonic acids are rarely found in drug candidate molecules, despite the potential of this
functional group to provide unique binding interactions with a target enzyme or receptor …

Selective intracellular activation of a novel prodrug of the human immunodeficiency virus reverse transcriptase inhibitor tenofovir leads to preferential distribution and …

WA Lee, GX He, E Eisenberg, T Cihlar… - Antimicrobial agents …, 2005 - Am Soc Microbiol
An isopropylalaninyl monoamidate phenyl monoester prodrug of tenofovir (GS 7340) was
prepared, and its in vitro antiviral activity, metabolism, and pharmacokinetics in dogs were …

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 …

Characterization of the transport of nucleoside analog drugs by the human multidrug resistance proteins MRP4 and MRP5

G Reid, P Wielinga, N Zelcer, M De Haas… - Molecular …, 2003 - ASPET
The human multidrug resistance proteins MRP4 and MRP5 are organic anion transporters
that have the unusual ability to transport cyclic nucleotides and some nucleoside …

Aryloxy phosphoramidate triesters: a technology for delivering monophosphorylated nucleosides and sugars into cells

Y Mehellou, J Balzarini… - … : Chemistry Enabling Drug …, 2009 - Wiley Online Library
Prodrug technologies aimed at delivering nucleoside monophosphates into cells (protides)
have proved to be effective in improving the therapeutic potential of antiviral and anticancer …