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Effects of structure on inhibitory activity in a series of mechanism-based inhibitors of human neutrophil elastase

Bioorganic & medicinal chemistry, 2010-09, Vol.18 (18), p.6646-6650

2010

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Characterization of a Novel 8-Oxoguanine-DNA Glycosylase Activity in Escherichia coli and Identification of the Enzyme as Endonuclease VIII

The Journal of biological chemistry, 2000-09, Vol.275 (36), p.27762-27767

2000

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Structure-Based Design of a General Class of Mechanism-Based Inhibitors of the Serine Proteinases Employing a Novel Amino Acid-Derived Heterocyclic Scaffold

Biochemistry (Easton), 1997-04, Vol.36 (16), p.4739-4750

1997

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Substituted 3-oxo-1,2,5-Thiadiazolidine 1,1-Dioxides: A New Class of Potential Mechanism-Based Inhibitors of Human Leukocyte Elastase and Cathepsin G

Biochemical and biophysical research communications, 1994-01, Vol.198 (1), p.341-349

1994

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Isoxazoline derivatives as potential inhibitors of the proteolytic enzymes human leukocyte elastase, cathepsin G and proteinase 3: a structure-activity relationship study

Bioorganic & medicinal chemistry, 1995-02, Vol.3 (2), p.125-128

1995

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Novel Potential Mechanism-Based Inhibitors of Human Leukocyte Elastase and Cathepsin G: Derivatives of Isothiazolidin-3-one

Biochemical and biophysical research communications, 1993-12, Vol.197 (2), p.730-739

1993

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A general approach toward the design of mechanism-based inactivators of serine proteinases: inactivation of human leukocyte elastase by a phthalimide derivative

Bioorganic & medicinal chemistry letters, 1993-12, Vol.3 (12), p.2745-2750

1993

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Mechanism-Based Inhibitors of Serine Proteinases Based on the Gabriel-Colman Rearrangement

Biochemical and biophysical research communications, 1993-08, Vol.194 (3), p.1491-1499

1993

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Potent and Specific Inhibition of Human Leukocyte Elastase, Cathepsin G and Proteinase 3 by Sulfone Derivatives Employing the 1,2,5-Thiadiazolidin-3-one 1,1 Dioxide Scaffold

Bioorganic & medicinal chemistry, 1998-06, Vol.6 (6), p.661-671

1998

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Potent inhibition of serine proteases by heterocyclic sulfide derivatives of 1,2,5-thiadiazolidin-3-one 1,1 dioxide

Bioorganic & medicinal chemistry, 2000-07, Vol.8 (7), p.1713-1717

2000

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Utilization of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold in the design of potent inhibitors of serine proteases: SAR studies using carboxylates

Bioorganic & medicinal chemistry, 2000-05, Vol.8 (5), p.1005-1016

2000

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Use of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide and isothiazolidin-3-one 1,1 dioxide scaffolds in the design of potent inhibitors of serine proteinases

Bioorganic & medicinal chemistry letters, 1998-03, Vol.8 (5), p.539-544

1998

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1,2,5-Thiadiazolidin-3-one 1,1 Dioxide: A Powerful Scaffold for Probing the S′ Subsites of (Chymo)trypsin-Like Serine Proteases

Archives of biochemistry and biophysics, 2001-01, Vol.385 (1), p.162-169

2001

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Mechanism of action of Escherichia coli formamidopyrimidine N-glycosylase: Role of K155 in substrate binding and product release

Progress in Nucleic Acid Research and Molecular Biology, 2001, Vol.68, p.223-234

2001

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Design, synthesis, and in vitro inhibitory activity toward human leukocyte elastase, cathepsin G, and proteinase 3 of saccharin-derived sulfones and congeners

Bioorganic & medicinal chemistry, 1996-09, Vol.4 (9), p.1393-1400

1996

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3-(alkylthio)-N-hydroxysuccinimide derivatives : potent inhibitors of human leukocyte elastase

Biochimica et biophysica acta, 1993-08, Vol.1164 (3), p.283-288

1993

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Efficient inhibition of human leukocyte elastase and cathepsin G by saccharin derivatives

Journal of medicinal chemistry, 1993-10, Vol.36 (21), p.3178-3181

1993

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Amino Acid-Derived Phthalimide and Saccharin Derivatives as Inhibitors of Human Leukocyte Elastase, Cathepsin G, and Proteinase 3

Archives of biochemistry and biophysics, 1996-08, Vol.332 (2), p.335-340

1996

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Low molecular weight inhibitors of human neutrophil elastase and human neutrophil myeloperoxidase

Venkataraman, Radhika

1992

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Mechanism-based inhibition of human leukocyte elastase and cathepsin G by susbtituted dihydrouracils

Biochimica et biophysica acta. Molecular basis of disease, 1994-11, Vol.1227 (3), p.130-136

1994

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Design, synthesis and biological evaluation of succinimide derivatives as potential mechanism-based inhibitors of human leukocyte elastase, cathepsin G and proteinase 3

Bioorganic & medicinal chemistry, 1995-04, Vol.3 (4), p.375-381

1995

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Dual-action inhibitors of proteolytic enzymes: potential therapeutic agents for cystic fibrosis and related ailments

Bioorganic & medicinal chemistry, 1993-10, Vol.1 (4), p.273-277

1993

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Catalysis in Drug Design and Medicinal Chemistry

Transactions of the Kansas Academy of Science, 1995-05, Vol.98 (1/2), p.17

1995

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The Gabriel-Colman rearrangement in biological systems: design, synthesis and biological evaluation of phthalimide and saccharin derivatives as potential mechanism-based inhibitors of human leukocyte elastase, cathepsin G and proteinase 3

Bioorganic & medicinal chemistry, 1995-02, Vol.3 (2), p.187-193

1995

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Enantioselective inhibition of human leukocyte elastase

Archives of biochemistry and biophysics, 1992-08, Vol.297 (1), p.144-146

1992

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Effects of structure on inhibitory activity in a series of mechanism-based inhibitors of human neutrophil elastase

Characterization of a Novel 8-Oxoguanine-DNA Glycosylase Activity in Escherichia coli and Identification of the Enzyme as Endonuclease VIII

Structure-Based Design of a General Class of Mechanism-Based Inhibitors of the Serine Proteinases Employing a Novel Amino Acid-Derived Heterocyclic Scaffold

Substituted 3-oxo-1,2,5-Thiadiazolidine 1,1-Dioxides: A New Class of Potential Mechanism-Based Inhibitors of Human Leukocyte Elastase and Cathepsin G

Isoxazoline derivatives as potential inhibitors of the proteolytic enzymes human leukocyte elastase, cathepsin G and proteinase 3: a structure-activity relationship study

Novel Potential Mechanism-Based Inhibitors of Human Leukocyte Elastase and Cathepsin G: Derivatives of Isothiazolidin-3-one

A general approach toward the design of mechanism-based inactivators of serine proteinases: inactivation of human leukocyte elastase by a phthalimide derivative

Mechanism-Based Inhibitors of Serine Proteinases Based on the Gabriel-Colman Rearrangement

Potent and Specific Inhibition of Human Leukocyte Elastase, Cathepsin G and Proteinase 3 by Sulfone Derivatives Employing the 1,2,5-Thiadiazolidin-3-one 1,1 Dioxide Scaffold

Potent inhibition of serine proteases by heterocyclic sulfide derivatives of 1,2,5-thiadiazolidin-3-one 1,1 dioxide

Utilization of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold in the design of potent inhibitors of serine proteases: SAR studies using carboxylates

Use of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide and isothiazolidin-3-one 1,1 dioxide scaffolds in the design of potent inhibitors of serine proteinases

1,2,5-Thiadiazolidin-3-one 1,1 Dioxide: A Powerful Scaffold for Probing the S′ Subsites of (Chymo)trypsin-Like Serine Proteases

Mechanism of action of Escherichia coli formamidopyrimidine N-glycosylase: Role of K155 in substrate binding and product release

Design, synthesis, and in vitro inhibitory activity toward human leukocyte elastase, cathepsin G, and proteinase 3 of saccharin-derived sulfones and congeners

3-(alkylthio)-N-hydroxysuccinimide derivatives : potent inhibitors of human leukocyte elastase

Efficient inhibition of human leukocyte elastase and cathepsin G by saccharin derivatives

Amino Acid-Derived Phthalimide and Saccharin Derivatives as Inhibitors of Human Leukocyte Elastase, Cathepsin G, and Proteinase 3

Low molecular weight inhibitors of human neutrophil elastase and human neutrophil myeloperoxidase

Mechanism-based inhibition of human leukocyte elastase and cathepsin G by susbtituted dihydrouracils

Design, synthesis and biological evaluation of succinimide derivatives as potential mechanism-based inhibitors of human leukocyte elastase, cathepsin G and proteinase 3

Dual-action inhibitors of proteolytic enzymes: potential therapeutic agents for cystic fibrosis and related ailments

Catalysis in Drug Design and Medicinal Chemistry

The Gabriel-Colman rearrangement in biological systems: design, synthesis and biological evaluation of phthalimide and saccharin derivatives as potential mechanism-based inhibitors of human leukocyte elastase, cathepsin G and proteinase 3

Enantioselective inhibition of human leukocyte elastase

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