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Steven J. Coats

Emory University

24

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378

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Discovery of a Series of 2′-α-Fluoro,2′-β-bromo-ribonucleosides and Their Phosphoramidate Prodrugs as Potent Pan-Genotypic Inhibitors of Hepatitis C Virus

2019 Journal of Medicinal Chemistry
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Synthesis of Carbocyclic Nucleoside Analogues with Five-Membered Heterocyclic Nucleobases.

2015 ChemInform
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nettles jmedchem 2006 target fishing SI

2014
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Synthesis of Nucleoside Phosphate and Phosphonate Prodrugs

2014 ChemInform
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Synthesis of Nucleoside Phosphate and Phosphonate Prodrugs

2014 Chemical Reviews
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jm501291c si 001

2014
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1168 BL-8030: A NOVEL, POTENT, SELECTIVE, ORALLY AVAILABLE INHIBITOR OF HEPATITIS C VIRUS NS3/4A PROTEASE

2013 Journal of Hepatology
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Promédicaments à base de monophosphate de purine pour traiter les infections virales

2012
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Substrate mimicry: HIV-1 reverse transcriptase recognizes 6-modified-3'-azido-2',3'-dideoxyguanosine-5'-triphosphates as adenosine analogs.

2012 Nucleic Acids Research
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1210 GNS-227: A NEW POTENT AND SELECTIVE HCV NS3 PROTEASE INHIBITOR WITH A HIGH GENETIC BARRIER TO RESISTANCE

2011 Journal of Hepatology
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