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Origin of rebound virus in chronically SIV-infected Rhesus monkeys following treatment discontinuation

Nature communications, 2020-10, Vol.11 (1), p.5412-5412, Article 5412

2020

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Discovery of a 2′-fluoro-2′-C-methyl C-nucleotide HCV polymerase inhibitor and a phosphoramidate prodrug with favorable properties

Bioorganic & medicinal chemistry letters, 2017-04, Vol.27 (8), p.1840-1847

2017

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Preparation and biological evaluation of 1′-cyano-2′-C-methyl pyrimidine nucleosides as HCV NS5B polymerase inhibitors

Bioorganic & medicinal chemistry letters, 2014-07, Vol.24 (14), p.3092-3095

2014

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Synthesis and characterization of 1′-C-cyano-2′-fluoro-2′-C-methyl pyrimidine nucleosides as HCV polymerase inhibitors

Bioorganic & medicinal chemistry letters, 2015-03, Vol.25 (5), p.1040-1043

2015

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Effect of substitution on novel tricyclic HIV-1 integrase inhibitors

Bioorganic & medicinal chemistry letters, 2006-08, Vol.16 (15), p.4031-4035

2006

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Asymmetric Dipolar Cycloadditions of Me3SiCHN2. Synthesis of a Novel Class of Amino Acids: Azaprolines

Journal of the American Chemical Society, 1997-09, Vol.119 (35), p.8379-8380

1997

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Toll‐Like Receptor 8 Agonist GS‐9688 Induces Sustained Efficacy in the Woodchuck Model of Chronic Hepatitis B

Hepatology (Baltimore, Md.), 2021-01, Vol.73 (1), p.53-67

2021

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Discovery of GS-9688 (Selgantolimod) as a Potent and Selective Oral Toll-Like Receptor 8 Agonist for the Treatment of Chronic Hepatitis B

Journal of medicinal chemistry, 2020-09, Vol.63 (18), p.10188-10203

2020

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Highly Potent HCV NS4B Inhibitors with Activity against Multiple Genotypes

Journal of medicinal chemistry, 2014-03, Vol.57 (5), p.2161-2166

2014

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Synthesis of 1′-C-Cyano Pyrimidine Nucleosides and Characterization as HCV Polymerase Inhibitors

Nucleosides, nucleotides & nucleic acids, 2015-11, Vol.34 (11), p.763-785

2015

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Tricyclic HIV integrase inhibitors: VI. SAR studies of ‘benzyl flipped’ C3-substituted pyrroloquinolines

Bioorganic & medicinal chemistry letters, 2009-02, Vol.19 (4), p.1187-1190

2009

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Tricyclic HIV integrase inhibitors V. SAR studies on the benzyl moiety

Bioorganic & medicinal chemistry letters, 2009-04, Vol.19 (8), p.2263-2265

2009

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Tricyclic HIV integrase inhibitors: Potent and orally bioavailable C5-aza analogs

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (4), p.1388-1391

2008

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Asymmetric Dipolar Cycloadditions of Me 3 SiCHN 2 . Synthesis of a Novel Class of Amino Acids: Azaprolines

Journal of the American Chemical Society, 1997-09, Vol.119 (35), p.8379-8380

1997

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The application of trimethylsilyl diazomethane to the synthesis of optically active pyrazolines and related studies

Mish, Michael Robert

2001

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Effect of Substitution on Novel Tricyclic HIV-1 Integrase Inhibitors

ChemInform, 2006-11, Vol.37 (46), p.no-no

2006

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State-level tracking of COVID-19 in the United States

Nature communications, 2020-12, Vol.11 (1), p.6189-6189, Article 6189

2020

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Chlamydia retesting remains low among young women in Australia: an observational study using sentinel surveillance data, 2018-2022

Sexual health, 2024-02, Vol.21 (2)

2024

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Toward a Sustainable Marketplace: Expanding Options and Benefits for Consumers

Journal of research for consumers, 2011-01 (19), p.1

2011

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Best practices in retailing: Going global: Best practice strategy and brand development

Chain store age (1995), 1995-11, Vol.71 (11), p.76

1995

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Origin of rebound virus in chronically SIV-infected Rhesus monkeys following treatment discontinuation

Discovery of a 2′-fluoro-2′-C-methyl C-nucleotide HCV polymerase inhibitor and a phosphoramidate prodrug with favorable properties

Preparation and biological evaluation of 1′-cyano-2′-C-methyl pyrimidine nucleosides as HCV NS5B polymerase inhibitors

Synthesis and characterization of 1′-C-cyano-2′-fluoro-2′-C-methyl pyrimidine nucleosides as HCV polymerase inhibitors

Effect of substitution on novel tricyclic HIV-1 integrase inhibitors

Asymmetric Dipolar Cycloadditions of Me3SiCHN2. Synthesis of a Novel Class of Amino Acids: Azaprolines

Toll‐Like Receptor 8 Agonist GS‐9688 Induces Sustained Efficacy in the Woodchuck Model of Chronic Hepatitis B

Discovery of GS-9688 (Selgantolimod) as a Potent and Selective Oral Toll-Like Receptor 8 Agonist for the Treatment of Chronic Hepatitis B

Discovery of a Potent and Orally Bioavailable Cyclophilin Inhibitor Derived from the Sanglifehrin Macrocycle

Structure-guided discovery of a novel, potent, and orally bioavailable 3,5-dimethylisoxazole aryl-benzimidazole BET bromodomain inhibitor

Highly Potent HCV NS4B Inhibitors with Activity against Multiple Genotypes

Synthesis of 1′-C-Cyano Pyrimidine Nucleosides and Characterization as HCV Polymerase Inhibitors

Tricyclic HIV integrase inhibitors: VI. SAR studies of ‘benzyl flipped’ C3-substituted pyrroloquinolines

Tricyclic HIV integrase inhibitors V. SAR studies on the benzyl moiety

Tricyclic HIV integrase inhibitors: Potent and orally bioavailable C5-aza analogs

Asymmetric Dipolar Cycloadditions of Me 3 SiCHN 2 . Synthesis of a Novel Class of Amino Acids: Azaprolines

The application of trimethylsilyl diazomethane to the synthesis of optically active pyrazolines and related studies

Effect of Substitution on Novel Tricyclic HIV-1 Integrase Inhibitors

State-level tracking of COVID-19 in the United States

Chlamydia retesting remains low among young women in Australia: an observational study using sentinel surveillance data, 2018-2022

Toward a Sustainable Marketplace: Expanding Options and Benefits for Consumers

Best practices in retailing: Going global: Best practice strategy and brand development

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