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Telavancin Disrupts the Functional Integrity of the Bacterial Membrane through Targeted Interaction with the Cell Wall Precursor Lipid II

Antimicrobial Agents and Chemotherapy, 2009-08, Vol.53 (8), p.3375-3383

2009

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Specificity of Induction of the vanA and vanB Operons in Vancomycin-Resistant Enterococci by Telavancin

Antimicrobial Agents and Chemotherapy, 2010-07, Vol.54 (7), p.2814-2818

2010

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Efficacy of telavancin, a lipoglycopeptide antibiotic, in experimental models of Gram-positive infection

Expert review of anti-infective therapy, 2014-12, Vol.12 (12), p.1463-1475

2014

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3,4-Disubstituted azetidinones as selective inhibitors of the cysteine protease cathepsin K. Exploring P3 elements for potency and selectivity

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1529-1534

2005

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Factor VIIa inhibitors: Chemical optimization, preclinical pharmacokinetics, pharmacodynamics, and efficacy in an arterial baboon thrombosis model

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (7), p.2037-2041

2006

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Quinolones as HCV NS5B polymerase inhibitors

Bioorganic & medicinal chemistry letters, 2011-01, Vol.21 (1), p.82-87

2011

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Keto-1,3,4-oxadiazoles as cathepsin K inhibitors

Bioorganic & medicinal chemistry letters, 2006-06, Vol.16 (11), p.2909-2914

2006

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Optimization of Subsite Binding to the β5 Subunit of the Human 20S Proteasome Using Vinyl Sulfones and 2-Keto-1,3,4-oxadiazoles: Syntheses and Cellular Properties of Potent, Selective Proteasome Inhibitors

Journal of medicinal chemistry, 2006-05, Vol.49 (10), p.2953-2968

2006

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3-Heterocyclyl quinolone inhibitors of the HCV NS5B polymerase

Bioorganic & medicinal chemistry letters, 2012-01, Vol.22 (1), p.300-304

2012

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Synthesis of a statistically exhaustive fluorescent peptide substrate library for profiling protease specificity

Bioorganic & medicinal chemistry letters, 2000-12, Vol.10 (23), p.2639-2642

2000

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Impact of telavancin on prothrombin time and activated partial thromboplastin time as determined using point-of-care coagulometers

Journal of thrombosis and thrombolysis, 2014, Vol.38 (2), p.235-240

2014

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Peptide Ketobenzoxazole Inhibitors Bound to Cathepsin K

Biochemistry (Easton), 2003-12, Vol.42 (51), p.15018-15028

2003

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Dissecting and Designing Inhibitor Selectivity Determinants at the S1 Site Using an Artificial Ala190 Protease (Ala190 uPA)

Journal of molecular biology, 2004-11, Vol.344 (2), p.527-547

2004

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Structure-Guided Design of Peptide-Based Tryptase Inhibitors

Biochemistry (Easton), 2006-05, Vol.45 (19), p.5964-5973

2006

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The ITK Inhibitor Cpi-818 Blocks Activation of T Cells from Autoimmune Lymphoproliferative Syndrome (ALPS) Patients and Is Active in a Murine Model of ALPS

Blood, 2020-11, Vol.136 (Supplement 1), p.36-37

2020

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Expression and characterization of recombinant γ-tryptase

Protein expression and purification, 2006-09, Vol.49 (1), p.47-54

2006

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Structure-activity relationship studies of a bisbenzimidazole-based, Zn2+-dependent inhibitor of HCV NS3 serine protease

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (17), p.2355-2359

2001

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Practical Robust Fit of Enzyme Inhibition Data

Methods in Enzymology, 2004, Vol.383, p.366-381

2004

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High-Throughput Screening of Enzyme Inhibitors: Simultaneous Determination of Tight-Binding Inhibition Constants and Enzyme Concentration

Analytical biochemistry, 2000-11, Vol.286 (1), p.45-50

2000

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Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-directed Serine Protease Inhibitors

Journal of molecular biology, 2003-05, Vol.329 (1), p.93-120

2003

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Highly Selective Irreversible ITK Inhibitor Cpi-818 Reduces Acute Graft-Versus Host Disease

Blood, 2021-11, Vol.138 (Supplement 1), p.3814-3814

2021

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Factor VIIa inhibitors: Gaining selectivity within the trypsin family

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (6), p.1596-1600

2006

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Interleukin-2-Inducible T-Cell Kinase (ITK) Inhibitors for the Treatment of T-Cell Lymphoproliferative Disorders

Blood, 2018-11, Vol.132 (Supplement 1), p.4172-4172

2018

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Highly potent non-peptidic inhibitors of the HCV NS3/NS4A serine protease

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (21), p.3129-3133

2002

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Design of novel, potent, and selective human β-tryptase inhibitors based on α-keto-[1,2,4]-oxadiazoles

Bioorganic & medicinal chemistry letters, 2006-08, Vol.16 (15), p.4036-4040

2006

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Telavancin Disrupts the Functional Integrity of the Bacterial Membrane through Targeted Interaction with the Cell Wall Precursor Lipid II

Specificity of Induction of the vanA and vanB Operons in Vancomycin-Resistant Enterococci by Telavancin

Efficacy of telavancin, a lipoglycopeptide antibiotic, in experimental models of Gram-positive infection

3,4-Disubstituted azetidinones as selective inhibitors of the cysteine protease cathepsin K. Exploring P3 elements for potency and selectivity

Factor VIIa inhibitors: Chemical optimization, preclinical pharmacokinetics, pharmacodynamics, and efficacy in an arterial baboon thrombosis model

Quinolones as HCV NS5B polymerase inhibitors

Keto-1,3,4-oxadiazoles as cathepsin K inhibitors

Optimization of Subsite Binding to the β5 Subunit of the Human 20S Proteasome Using Vinyl Sulfones and 2-Keto-1,3,4-oxadiazoles: Syntheses and Cellular Properties of Potent, Selective Proteasome Inhibitors

3-Heterocyclyl quinolone inhibitors of the HCV NS5B polymerase

Synthesis of a statistically exhaustive fluorescent peptide substrate library for profiling protease specificity

Impact of telavancin on prothrombin time and activated partial thromboplastin time as determined using point-of-care coagulometers

Peptide Ketobenzoxazole Inhibitors Bound to Cathepsin K

Dissecting and Designing Inhibitor Selectivity Determinants at the S1 Site Using an Artificial Ala190 Protease (Ala190 uPA)

Structure-Guided Design of Peptide-Based Tryptase Inhibitors

The ITK Inhibitor Cpi-818 Blocks Activation of T Cells from Autoimmune Lymphoproliferative Syndrome (ALPS) Patients and Is Active in a Murine Model of ALPS

Expression and characterization of recombinant γ-tryptase

Structure-activity relationship studies of a bisbenzimidazole-based, Zn2+-dependent inhibitor of HCV NS3 serine protease

Practical Robust Fit of Enzyme Inhibition Data

High-Throughput Screening of Enzyme Inhibitors: Simultaneous Determination of Tight-Binding Inhibition Constants and Enzyme Concentration

Elaborate Manifold of Short Hydrogen Bond Arrays Mediating Binding of Active Site-directed Serine Protease Inhibitors

Highly Selective Irreversible ITK Inhibitor Cpi-818 Reduces Acute Graft-Versus Host Disease

Factor VIIa inhibitors: Gaining selectivity within the trypsin family

Interleukin-2-Inducible T-Cell Kinase (ITK) Inhibitors for the Treatment of T-Cell Lymphoproliferative Disorders

Highly potent non-peptidic inhibitors of the HCV NS3/NS4A serine protease

Design of novel, potent, and selective human β-tryptase inhibitors based on α-keto-[1,2,4]-oxadiazoles

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