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Inhibitors of HIV-1 Protease by Using In Situ Click Chemistry

Angewandte Chemie International Edition, 2006-02, Vol.45 (9), p.1435-1439

2006

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1,2,3-Triazole as a Peptide Surrogate in the Rapid Synthesis of HIV-1 Protease Inhibitors

Chembiochem : a European journal of chemical biology, 2005-07, Vol.6 (7), p.1167-1169

2005

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Crucial structural parameters affecting electrochemical properties of activated electrospun carbon fibers as solid-state supercapacitor electrodes

Journal of materials science, 2023-10, Vol.58 (38), p.15144-15161

2023

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Conformational flexibility in the flap domains of ligand-free HIV protease

Acta crystallographica. Section D, Biological crystallography., 2007-08, Vol.63 (8), p.866-875

2007

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Feline immunodeficiency virus (FIV) as a model for study of lentivirus infections: parallels with HIV

Current HIV research, 2010-01, Vol.8 (1), p.73-80

2010

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Selection of Drug-Resistant Feline Immunodeficiency Virus (FIV) Encoding FIV/HIV Chimeric Protease in the Presence of HIV-Specific Protease Inhibitors

Journal of Virology, 2013-08, Vol.87 (15), p.8524-8534

2013

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Rapid Diversity-Oriented Synthesis in Microtiter Plates for In Situ Screening of HIV Protease Inhibitors

Chembiochem : a European journal of chemical biology, 2003-11, Vol.4 (11), p.1246-1248

2003

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Small Molecule Regulation of Protein Conformation by Binding in the Flap of HIV Protease

ACS chemical biology, 2013-06, Vol.8 (6), p.1223-1231

2013

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A Copper(I)-Catalyzed 1,2,3-Triazole Azide−Alkyne Click Compound Is a Potent Inhibitor of a Multidrug-Resistant HIV-1 Protease Variant

Journal of medicinal chemistry, 2008-10, Vol.51 (20), p.6263-6270

2008

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Generation of Infectious Feline Immunodeficiency Virus (FIV) Encoding FIV/Human Immunodeficiency Virus Chimeric Protease

Journal of Virology, 2010-07, Vol.84 (13), p.6799-6809

2010

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Rapid Discovery and Structure−Activity Profiling of Novel Inhibitors of Human Immunodeficiency Virus Type 1 Protease Enabled by the Copper(I)-Catalyzed Synthesis of 1,2,3-Triazoles and Their Further Functionalization

Journal of medicinal chemistry, 2006-12, Vol.49 (26), p.7697-7710

2006

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Altered Gag Polyprotein Cleavage Specificity of Feline Immunodeficiency Virus/Human Immunodeficiency Virus Mutant Proteases as Demonstrated in a Cell-Based Expression System

Journal of Virology, 2006-08, Vol.80 (16), p.7832-7843

2006

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Epoxide opening in water and screening in situ for rapid discovery of enzyme inhibitors in microtiter plates

Bioorganic & medicinal chemistry, 2006-02, Vol.14 (4), p.1058-1062

2006

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Structural basis for drug and substrate specificity exhibited by FIV encoding a chimeric FIV/HIV protease

Acta crystallographica. Section D, Biological crystallography., 2011-06, Vol.67 (6), p.540-548

2011

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Structural Basis for Distinctions between Substrate and Inhibitor Specificities for Feline Immunodeficiency Virus and Human Immunodeficiency Virus Proteases

Journal of Virology, 2003-06, Vol.77 (12), p.6589-6600

2003

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Crystal structure of an FIV/HIV chimeric protease complexed with the broad-based inhibitor, TL-3

Retrovirology, 2007-01, Vol.4 (1), p.1-1, Article 1

2007

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Resolution and Prevention of Feline Immunodeficiency Virus-Induced Neurological Deficits by Treatment with the Protease Inhibitor TL-3

Journal of Virology, 2004-05, Vol.78 (9), p.4525-4532

2004

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Assessment of FIV-C infection of cats as a function of treatment with the protease inhibitor, TL-3

Retrovirology, 2004-11, Vol.1 (1), p.38-38, Article 38

2004

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Molecular mechanisms of FIV infection

Veterinary immunology and immunopathology, 2008-05, Vol.123 (1), p.3-13

2008

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Development of a New Type of Protease Inhibitors, Efficacious against FIV and HIV Variants

Journal of the American Chemical Society, 1999-02, Vol.121 (6), p.1145-1155

1999

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Alteration of Substrate and Inhibitor Specificity of Feline Immunodeficiency Virus Protease

Journal of Virology, 2000-05, Vol.74 (10), p.4710-4720

2000

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The Effect of Tetrandrine and Extracts of Centella asiatica on Acute Radiation Dermatitis in Rats

Biological and Pharmaceutical Bulletin, 1999/07/15, Vol.22(7), pp.703-706

1999

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Structural Insights into the Mechanisms of Drug Resistance in HIV-1 Protease NL4-3

Journal of molecular biology, 2006-03, Vol.356 (4), p.967-981

2006

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Molecular Basis for the Relative Substrate Specificity of Human Immunodeficiency Virus Type 1 and Feline Immunodeficiency Virus Proteases

Journal of Virology, 2001-10, Vol.75 (19), p.9458-9469

2001

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Cover Picture: 1,2,3-Triazole as a Peptide Surrogate in the Rapid Synthesis of HIV-1 Protease Inhibitors (ChemBioChem 7/2005)

Chembiochem : a European journal of chemical biology, 2005-07, Vol.6 (7), p.1137-1137

2005

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Inhibitors of HIV-1 Protease by Using In Situ Click Chemistry

1,2,3-Triazole as a Peptide Surrogate in the Rapid Synthesis of HIV-1 Protease Inhibitors

Crucial structural parameters affecting electrochemical properties of activated electrospun carbon fibers as solid-state supercapacitor electrodes

Conformational flexibility in the flap domains of ligand-free HIV protease

Feline immunodeficiency virus (FIV) as a model for study of lentivirus infections: parallels with HIV

Selection of Drug-Resistant Feline Immunodeficiency Virus (FIV) Encoding FIV/HIV Chimeric Protease in the Presence of HIV-Specific Protease Inhibitors

Rapid Diversity-Oriented Synthesis in Microtiter Plates for In Situ Screening of HIV Protease Inhibitors

Small Molecule Regulation of Protein Conformation by Binding in the Flap of HIV Protease

A Copper(I)-Catalyzed 1,2,3-Triazole Azide−Alkyne Click Compound Is a Potent Inhibitor of a Multidrug-Resistant HIV-1 Protease Variant

Generation of Infectious Feline Immunodeficiency Virus (FIV) Encoding FIV/Human Immunodeficiency Virus Chimeric Protease

Rapid Discovery and Structure−Activity Profiling of Novel Inhibitors of Human Immunodeficiency Virus Type 1 Protease Enabled by the Copper(I)-Catalyzed Synthesis of 1,2,3-Triazoles and Their Further Functionalization

Altered Gag Polyprotein Cleavage Specificity of Feline Immunodeficiency Virus/Human Immunodeficiency Virus Mutant Proteases as Demonstrated in a Cell-Based Expression System

Epoxide opening in water and screening in situ for rapid discovery of enzyme inhibitors in microtiter plates

Structural basis for drug and substrate specificity exhibited by FIV encoding a chimeric FIV/HIV protease

Structural Basis for Distinctions between Substrate and Inhibitor Specificities for Feline Immunodeficiency Virus and Human Immunodeficiency Virus Proteases

Crystal structure of an FIV/HIV chimeric protease complexed with the broad-based inhibitor, TL-3

Resolution and Prevention of Feline Immunodeficiency Virus-Induced Neurological Deficits by Treatment with the Protease Inhibitor TL-3

Assessment of FIV-C infection of cats as a function of treatment with the protease inhibitor, TL-3

Molecular mechanisms of FIV infection

Development of a New Type of Protease Inhibitors, Efficacious against FIV and HIV Variants

Alteration of Substrate and Inhibitor Specificity of Feline Immunodeficiency Virus Protease

The Effect of Tetrandrine and Extracts of Centella asiatica on Acute Radiation Dermatitis in Rats

Structural Insights into the Mechanisms of Drug Resistance in HIV-1 Protease NL4-3

Molecular Basis for the Relative Substrate Specificity of Human Immunodeficiency Virus Type 1 and Feline Immunodeficiency Virus Proteases

Cover Picture: 1,2,3-Triazole as a Peptide Surrogate in the Rapid Synthesis of HIV-1 Protease Inhibitors (ChemBioChem 7/2005)

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