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Reversible Cysteine Protease Inhibitors Show Promise for a Chagas Disease Cure

Antimicrobial Agents and Chemotherapy, 2014-02, Vol.58 (2), p.1167-1178

2014

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The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (3), p.923-928

2008

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A Role for the Malonyl-CoA/Long-Chain Acyl-CoA Pathway of Lipid Signaling in the Regulation of Insulin Secretion in Response to Both Fuel and Nonfuel Stimuli

Diabetes (New York, N.Y.), 2004-04, Vol.53 (4), p.1007-1019

2004

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Pharmacological inhibitors to identify roles of cathepsin K in cell-based studies: a comparison of available tools

Biological chemistry, 2009-09, Vol.390 (9), p.941-948

2009

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Discovery of disubstituted phenanthrene imidazoles as potent, selective and orally active mPGES-1 inhibitors

Bioorganic & medicinal chemistry letters, 2009-10, Vol.19 (20), p.5837-5841

2009

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The Discovery of Setileuton, a Potent and Selective 5-Lipoxygenase Inhibitor

ACS medicinal chemistry letters, 2010-07, Vol.1 (4), p.170-174

2010

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Application of the Protein Maker as a platform purification system for therapeutic antibody research and development

Computational and structural biotechnology journal, 2016-01, Vol.14 (C), p.238-244

2016

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Substituted phenanthrene imidazoles as potent, selective, and orally active mPGES-1 inhibitors

Bioorganic & medicinal chemistry letters, 2007-12, Vol.17 (24), p.6816-6820

2007

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Gold mining in Colombia, post-war crime and the peace agreement with the FARC

Third world thematics : a TWQ journal, 2018-01, Vol.3 (1), p.116-134

2018

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The identification of potent, selective, and bioavailable cathepsin S inhibitors

Bioorganic & medicinal chemistry letters, 2007-09, Vol.17 (17), p.4929-4933

2007

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Trifluoroethylamines as amide isosteres in inhibitors of cathepsin K

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (21), p.4741-4744

2005

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Difluoroethylamines as an amide isostere in inhibitors of cathepsin K

Bioorganic & medicinal chemistry letters, 2011-02, Vol.21 (3), p.920-923

2011

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War Economies and Post-war Crime

1, 2020

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Identification of potent and reversible cruzipain inhibitors for the treatment of Chagas disease

Bioorganic & medicinal chemistry letters, 2010-12, Vol.20 (24), p.7444-7449

2010

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Synthesis and biological activity of a potent and orally bioavailable SCD inhibitor (MF-438)

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (2), p.499-502

2010

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Identification of a Nonbasic, Nitrile-Containing Cathepsin K Inhibitor (MK-1256) that is Efficacious in a Monkey Model of Osteoporosis

Journal of medicinal chemistry, 2008-10, Vol.51 (20), p.6410-6420

2008

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La guerre est finie

Politique internationale, 2017-01 (154)

Massé, Frédéric

2017

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Colombie : le repos des guerriers

Politique internationale, 2017-01 (154)

Massé, Frédéric

2017

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Glucose Down-regulates the Expression of the Peroxisome Proliferator-activated Receptor-α Gene in the Pancreatic β-Cell

The Journal of biological chemistry, 2000-11, Vol.275 (46), p.35799-35806

2000

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Activation of Malonyl-CoA Decarboxylase in Rat Skeletal Muscle by Contraction and the AMP-activated Protein Kinase Activator 5-Aminoimidazole-4-carboxamide-1-β-d-ribofuranoside

The Journal of biological chemistry, 2000-08, Vol.275 (32), p.24279-24283

2000

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POPKIN (Margareth) – Peace without Justice, Obstacles to Building the Rule of Law in El Salvador . – University Park, Pennsylvania State University Press, 2000. 287 p

Revue française de science politique, 2003-12, Vol.53 (6), p.V-V

Massé, Frédéric

2003

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Identification of a potent and selective non-basic cathepsin K inhibitor

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (7), p.1985-1989

2006

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Lysosomotropism of Basic Cathepsin K Inhibitors Contributes to Increased Cellular Potencies against Off-Target Cathepsins and Reduced Functional Selectivity

Journal of medicinal chemistry, 2005-12, Vol.48 (24), p.7535-7543

2005

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Investigation of ketone warheads as alternatives to the nitrile for preparation of potent and selective cathepsin K inhibitors

Bioorganic & medicinal chemistry letters, 2009-02, Vol.19 (3), p.675-679

2009

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Primary amides as selective inhibitors of cathepsin K

Bioorganic & medicinal chemistry letters, 2007-08, Vol.17 (15), p.4328-4332

2007

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Reversible Cysteine Protease Inhibitors Show Promise for a Chagas Disease Cure

The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K

A Role for the Malonyl-CoA/Long-Chain Acyl-CoA Pathway of Lipid Signaling in the Regulation of Insulin Secretion in Response to Both Fuel and Nonfuel Stimuli

Pharmacological inhibitors to identify roles of cathepsin K in cell-based studies: a comparison of available tools

Discovery of disubstituted phenanthrene imidazoles as potent, selective and orally active mPGES-1 inhibitors

The Discovery of Setileuton, a Potent and Selective 5-Lipoxygenase Inhibitor

Application of the Protein Maker as a platform purification system for therapeutic antibody research and development

Substituted phenanthrene imidazoles as potent, selective, and orally active mPGES-1 inhibitors

Gold mining in Colombia, post-war crime and the peace agreement with the FARC

The identification of potent, selective, and bioavailable cathepsin S inhibitors

Trifluoroethylamines as amide isosteres in inhibitors of cathepsin K

Difluoroethylamines as an amide isostere in inhibitors of cathepsin K

War Economies and Post-war Crime

Identification of potent and reversible cruzipain inhibitors for the treatment of Chagas disease

Synthesis and biological activity of a potent and orally bioavailable SCD inhibitor (MF-438)

Identification of a Nonbasic, Nitrile-Containing Cathepsin K Inhibitor (MK-1256) that is Efficacious in a Monkey Model of Osteoporosis

La guerre est finie

Colombie : le repos des guerriers

Glucose Down-regulates the Expression of the Peroxisome Proliferator-activated Receptor-α Gene in the Pancreatic β-Cell

Activation of Malonyl-CoA Decarboxylase in Rat Skeletal Muscle by Contraction and the AMP-activated Protein Kinase Activator 5-Aminoimidazole-4-carboxamide-1-β-d-ribofuranoside

POPKIN (Margareth) – Peace without Justice, Obstacles to Building the Rule of Law in El Salvador . – University Park, Pennsylvania State University Press, 2000. 287 p

Identification of a potent and selective non-basic cathepsin K inhibitor

Lysosomotropism of Basic Cathepsin K Inhibitors Contributes to Increased Cellular Potencies against Off-Target Cathepsins and Reduced Functional Selectivity

Investigation of ketone warheads as alternatives to the nitrile for preparation of potent and selective cathepsin K inhibitors

Primary amides as selective inhibitors of cathepsin K

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