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In Vitro Antiretroviral Properties of S/GSK1349572, a Next-Generation HIV Integrase Inhibitor

Antimicrobial Agents and Chemotherapy, 2011-02, Vol.55 (2), p.813-821

2011

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Structure−Activity Relationship Studies of Novel Benzophenones Leading to the Discovery of a Potent, Next Generation HIV Nonnucleoside Reverse Transcriptase Inhibitor

Journal of medicinal chemistry, 2006-01, Vol.49 (2), p.727-739

2006

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The Naphthyridinone GSK364735 Is a Novel, Potent Human Immunodeficiency Virus Type 1 Integrase Inhibitor and Antiretroviral

Antimicrobial Agents and Chemotherapy, 2008-03, Vol.52 (3), p.901-908

2008

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Antiviral Activity of GW678248, a Novel Benzophenone Nonnucleoside Reverse Transcriptase Inhibitor

Antimicrobial Agents and Chemotherapy, 2005-10, Vol.49 (10), p.4046-4051

2005

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Anti-Human Immunodeficiency Virus Type 1 Activity of the Nonnucleoside Reverse Transcriptase Inhibitor GW678248 in Combination with Other Antiretrovirals against Clinical Isolate Viruses and In Vitro Selection for Resistance

Antimicrobial Agents and Chemotherapy, 2005-11, Vol.49 (11), p.4465-4473

2005

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Design of Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase with Improved Drug Resistance Properties. 1

Journal of medicinal chemistry, 2004-11, Vol.47 (24), p.5912-5922

2004

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Synthesis and Antiviral Activity of 7-Benzyl-4-hydroxy-1,5-naphthyridin-2(1H)-one HIV Integrase Inhibitors

Journal of medicinal chemistry, 2009-05, Vol.52 (9), p.2754-2761

2009

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Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: The discovery of GW0385

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (7), p.1788-1794

2006

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Design of Non-nucleoside Inhibitors of HIV-1 Reverse Transcriptase with Improved Drug Resistance Properties. 2

Journal of medicinal chemistry, 2004-11, Vol.47 (24), p.5923-5936

2004

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2-Amino-6-arylsulfonylbenzonitriles as Non-nucleoside Reverse Transcriptase Inhibitors of HIV-1

Journal of medicinal chemistry, 2001-06, Vol.44 (12), p.1866-1882

2001

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Novel Benzophenones as Non-nucleoside Reverse Transcriptase Inhibitors of HIV-1

Journal of medicinal chemistry, 2004-02, Vol.47 (5), p.1175-1182

2004

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Novel P1 chain-extended HIV protease inhibitors possessing potent anti-HIV activity and remarkable inverse antiviral resistance profiles

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (15), p.3496-3500

2005

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Novel arylsulfonamides possessing sub-picomolar HIV protease activities and potent anti-HIV activity against wild-type and drug-resistant viral strains

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (4), p.959-963

2004

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Synthesis and antiviral activities of novel N-alkoxy-arylsulfonamide-based HIV protease inhibitors

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (15), p.3560-3564

2005

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The Naphthyridinone GSK364735 Is a Novel, Potent Human Immunodeficiency Virus Type 1 Integrase Inhibitor and Antiretroviral

Antimicrobial agents and chemotherapy, 2008-05, Vol.52 (5), p.1899-1899

2008

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Optimization of pyrrolidinone based HIV protease inhibitors

Bioorganic & medicinal chemistry letters, 2005-01, Vol.15 (1), p.81-84

2005

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Synthesis of Potential Anti-HIV GP120 Inhibitors Using a Lysine Template

Journal of enzyme inhibition and medicinal chemistry, 2002-06, Vol.17 (3), p.175-182

2002

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Inhibitors of Human Immunodeficiency Virus Type 1 Derived from gp41 Transmembrane Protein: Structure−Activity Studies

Journal of medicinal chemistry, 1996-07, Vol.39 (14), p.2681-2689

1996

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Novel inhibitors of HIV protease : Design, synthesis and biological evaluation of picomolar inhibitors containing cyclic P1/P2 scaffolds

Bioorganic & medicinal chemistry letters, 2000-06, Vol.10 (11), p.1159-1162

2000

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Novel inhibitors of HIV protease

Bioorganic & medicinal chemistry letters, 2000-06, Vol.10 (11), p.1159-1162

2000

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Sodium azide protects against ischemia-induced acute renal failure in rats

American journal of physiology. Renal physiology, 1993-07, Vol.34 (1), p.F130

1993

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Sodium azide protects against ischemia-induced acute renal failure in rats

American journal of physiology. Renal physiology, 1993-07, Vol.265 (1), p.130-F136

1993

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Novel Arylsulfonamides Possessing Sub-Picomolar HIV Protease Activities and Potent anti-HIV Activity against Wild-Type and Drug-Resistant Viral Strains

ChemInform, 2004-06, Vol.35 (23), p.no-no

2004

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ChemInform Abstract: Novel Inhibitors of HIV Protease: Design, Synthesis and Biological Evaluation of Picomolar Inhibitors Containing Cyclic P1/P2 Scaffolds

ChemInform, 2000-09, Vol.31 (39), p.no-no

2000

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The TMAO-Generating Enzyme Flavin Monooxygenase 3 Is a Central Regulator of Cholesterol Balance

Cell reports (Cambridge), 2015-01, Vol.10 (3), p.326-338

2015

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In Vitro Antiretroviral Properties of S/GSK1349572, a Next-Generation HIV Integrase Inhibitor

Structure−Activity Relationship Studies of Novel Benzophenones Leading to the Discovery of a Potent, Next Generation HIV Nonnucleoside Reverse Transcriptase Inhibitor

The Naphthyridinone GSK364735 Is a Novel, Potent Human Immunodeficiency Virus Type 1 Integrase Inhibitor and Antiretroviral

Antiviral Activity of GW678248, a Novel Benzophenone Nonnucleoside Reverse Transcriptase Inhibitor

Anti-Human Immunodeficiency Virus Type 1 Activity of the Nonnucleoside Reverse Transcriptase Inhibitor GW678248 in Combination with Other Antiretrovirals against Clinical Isolate Viruses and In Vitro Selection for Resistance

Design of Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase with Improved Drug Resistance Properties. 1

Synthesis and Antiviral Activity of 7-Benzyl-4-hydroxy-1,5-naphthyridin-2(1H)-one HIV Integrase Inhibitors

Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: The discovery of GW0385

Design of Non-nucleoside Inhibitors of HIV-1 Reverse Transcriptase with Improved Drug Resistance Properties. 2

2-Amino-6-arylsulfonylbenzonitriles as Non-nucleoside Reverse Transcriptase Inhibitors of HIV-1

Novel Benzophenones as Non-nucleoside Reverse Transcriptase Inhibitors of HIV-1

Novel P1 chain-extended HIV protease inhibitors possessing potent anti-HIV activity and remarkable inverse antiviral resistance profiles

Novel arylsulfonamides possessing sub-picomolar HIV protease activities and potent anti-HIV activity against wild-type and drug-resistant viral strains

Synthesis and antiviral activities of novel N-alkoxy-arylsulfonamide-based HIV protease inhibitors

The Naphthyridinone GSK364735 Is a Novel, Potent Human Immunodeficiency Virus Type 1 Integrase Inhibitor and Antiretroviral

Optimization of pyrrolidinone based HIV protease inhibitors

Synthesis of Potential Anti-HIV GP120 Inhibitors Using a Lysine Template

Inhibitors of Human Immunodeficiency Virus Type 1 Derived from gp41 Transmembrane Protein: Structure−Activity Studies

Novel inhibitors of HIV protease : Design, synthesis and biological evaluation of picomolar inhibitors containing cyclic P1/P2 scaffolds

Novel inhibitors of HIV protease

Sodium azide protects against ischemia-induced acute renal failure in rats

Sodium azide protects against ischemia-induced acute renal failure in rats

Novel Arylsulfonamides Possessing Sub-Picomolar HIV Protease Activities and Potent anti-HIV Activity against Wild-Type and Drug-Resistant Viral Strains

ChemInform Abstract: Novel Inhibitors of HIV Protease: Design, Synthesis and Biological Evaluation of Picomolar Inhibitors Containing Cyclic P1/P2 Scaffolds

The TMAO-Generating Enzyme Flavin Monooxygenase 3 Is a Central Regulator of Cholesterol Balance

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