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The use of oxadiazole and triazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 1: Establishing the pharmacophore

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (6), p.1802-1806

2009

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1,3,4-Oxadiazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 2: SAR of the C5 position

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (6), p.1807-1810

2009

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Potent and Selective Inhibition of Human Cytomegalovirus Replication by 1263W94, a Benzimidazole l-Riboside with a Unique Mode of Action

Antimicrobial Agents and Chemotherapy, 2002-08, Vol.46 (8), p.2365-2372

2002

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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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Synthesis and HIV-integrase strand transfer inhibition activity of 7-hydroxy[1,3]thiazolo[5,4- b]pyridin-5(4 H)-ones

Bioorganic & medicinal chemistry letters, 2006-11, Vol.16 (21), p.5668-5672

2006

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Kinetic Analysis of Wild-Type and YMDD Mutant Hepatitis B Virus Polymerases and Effects of Deoxyribonucleotide Concentrations on Polymerase Activity

Antimicrobial Agents and Chemotherapy, 2002-04, Vol.46 (4), p.1005-1013

2002

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Acyclovir Is Phosphorylated by the Human Cytomegalovirus UL97 Protein

Antimicrobial Agents and Chemotherapy, 1999-08, Vol.43 (8), p.1941-1946

1999

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Late Presentation of Pulmonary Artery-Left Atrial Appendage Fistula Formation After Left Atrial Appendage Device Closure

JACC. Case reports, 2020-05, Vol.2 (5), p.814-818

2020

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Pseudoaneurysm as a Late Complication of Chronic Stanford Type A Intramural Hematoma Requiring Endovascular Repair

JACC. Case reports, 2020-12, Vol.2 (15), p.2470-2475

2020

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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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Combining symmetry elements results in potent naphthyridinone (NTD) HIV-1 integrase inhibitors

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6461-6464

2011

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Acyclic Guanosine Analogs Inhibit DNA Polymerases .alpha., .delta., and .epsilon. with Very Different Potencies and Have Unique Mechanisms of Action

Biochemistry (Easton), 1995-02, Vol.34 (8), p.2504-2510

1995

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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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1592U89, a novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity

Antimicrobial Agents and Chemotherapy, 1997-05, Vol.41 (5), p.1082-1093

1997

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Unique intracellular activation of the potent anti-human immunodeficiency virus agent 1592U89

Antimicrobial Agents and Chemotherapy, 1997-05, Vol.41 (5), p.1099-1107

1997

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Phosphorylation of acyclovir diphosphate by cellular enzymes

Biochemical pharmacology, 1982-12, Vol.31 (23), p.3879-3884

1982

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Inhibition of UDP-N-Acetylglucosamine Import into Golgi Membranes by Nucleoside Monophosphates

Journal of medicinal chemistry, 1996-07, Vol.39 (15), p.2894-2899

1996

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Human immunodeficiency virus reverse transcriptase. Substrate and inhibitor kinetics with thymidine 5'-triphosphate and 3'-azido-3'-deoxythymidine 5'-triphosphate

The Journal of biological chemistry, 1990-11, Vol.265 (33), p.20302-20307

1990

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Phosphorylation of carbovir enantiomers by cellular enzymes determines the stereoselectivity of antiviral activity

The Journal of biological chemistry, 1992-10, Vol.267 (29), p.21220-21224

1992

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Pseudoaneurysm as a Late Complication of Chronic Stanford Type A Intramural Hematoma Requiring Endovascular Repair

JACC. Case reports, 2020, Vol.2 (15), p.2470-2475

2020

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Late Presentation of Pulmonary Artery-Left Atrial Appendage Fistula Formation After Left Atrial Appendage Device Closure

JACC. Case reports, 2020, Vol.2 (5), p.814-818

2020

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DNA polymerase activity of hepatitis B virus particles: differential inhibition by l-enantiomers of nucleotide analogs

Antiviral research, 1996-05, Vol.30 (2), p.133-145

1996

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Preparation of some sulfonamide and diaminodiphenyl sulfone analogs of 1,4-naphthoquinone

Journal of medicinal chemistry, 1969-01, Vol.12 (1), p.187-189

1969

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Thiosemicarbazone and amidinohydrazone derivatives of some 1,4-naphthoquinones

Journal of the Chemical Society. C. Organic, 1970 (15), p.1993

1970

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What's an ERISA fiduciary to do?

Directors and Boards, 2005-10, Vol.30 (1), p.45

Miller, Wayne H

2005

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The use of oxadiazole and triazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 1: Establishing the pharmacophore

1,3,4-Oxadiazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 2: SAR of the C5 position

Potent and Selective Inhibition of Human Cytomegalovirus Replication by 1263W94, a Benzimidazole l-Riboside with a Unique Mode of Action

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

Synthesis and HIV-integrase strand transfer inhibition activity of 7-hydroxy[1,3]thiazolo[5,4- b]pyridin-5(4 H)-ones

Kinetic Analysis of Wild-Type and YMDD Mutant Hepatitis B Virus Polymerases and Effects of Deoxyribonucleotide Concentrations on Polymerase Activity

Acyclovir Is Phosphorylated by the Human Cytomegalovirus UL97 Protein

Late Presentation of Pulmonary Artery-Left Atrial Appendage Fistula Formation After Left Atrial Appendage Device Closure

Pseudoaneurysm as a Late Complication of Chronic Stanford Type A Intramural Hematoma Requiring Endovascular Repair

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

Combining symmetry elements results in potent naphthyridinone (NTD) HIV-1 integrase inhibitors

Acyclic Guanosine Analogs Inhibit DNA Polymerases .alpha., .delta., and .epsilon. with Very Different Potencies and Have Unique Mechanisms of Action

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

1592U89, a novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity

Unique intracellular activation of the potent anti-human immunodeficiency virus agent 1592U89

Phosphorylation of acyclovir diphosphate by cellular enzymes

Inhibition of UDP-N-Acetylglucosamine Import into Golgi Membranes by Nucleoside Monophosphates

Human immunodeficiency virus reverse transcriptase. Substrate and inhibitor kinetics with thymidine 5'-triphosphate and 3'-azido-3'-deoxythymidine 5'-triphosphate

Phosphorylation of carbovir enantiomers by cellular enzymes determines the stereoselectivity of antiviral activity

Pseudoaneurysm as a Late Complication of Chronic Stanford Type A Intramural Hematoma Requiring Endovascular Repair

Late Presentation of Pulmonary Artery-Left Atrial Appendage Fistula Formation After Left Atrial Appendage Device Closure

DNA polymerase activity of hepatitis B virus particles: differential inhibition by l-enantiomers of nucleotide analogs

Preparation of some sulfonamide and diaminodiphenyl sulfone analogs of 1,4-naphthoquinone

Thiosemicarbazone and amidinohydrazone derivatives of some 1,4-naphthoquinones

What's an ERISA fiduciary to do?

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