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Discovery of Fragment-Derived Small Molecules for in Vivo Inhibition of Ketohexokinase (KHK)

Journal of medicinal chemistry, 2017-09, Vol.60 (18), p.7835-7849

2017

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Discovery of PF-06835919: A Potent Inhibitor of Ketohexokinase (KHK) for the Treatment of Metabolic Disorders Driven by the Overconsumption of Fructose

Journal of medicinal chemistry, 2020-11, Vol.63 (22), p.13546-13560

2020

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Gestion durable des ressources en eau dans le secteur agricole

Publishing, OECD

1, 2010

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Crystal Structures of a Mutant (βK87T) Tryptophan Synthase α2β2 Complex with Ligands Bound to the Active Sites of the α- and β-Subunits Reveal Ligand-Induced Conformational Changes

Biochemistry (Easton), 1997-06, Vol.36 (25), p.7664-7680

1997

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Catalytically Active MAP KAP Kinase 2 Structures in Complex with Staurosporine and ADP Reveal Differences with the Autoinhibited Enzyme

Structure (London), 2003-06, Vol.11 (6), p.627-636

2003

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Exchange of K+ or Cs+ for Na+ Induces Local and Long-Range Changes in the Three-Dimensional Structure of the Tryptophan Synthase α2β2 Complex

Biochemistry (Easton), 1996-04, Vol.35 (13), p.4211-4221

1996

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Kinetics and Mechanism of Autoprocessing of Human Immunodeficiency Virus Type 1 Protease from an Analog of the Gag-Pol Polyprotein

Proceedings of the National Academy of Sciences - PNAS, 1994-08, Vol.91 (17), p.7970-7974

1994

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Ligand-mediated Changes in the Tryptophan Synthase Indole Tunnel Probed by Nile Red Fluorescence with Wild Type, Mutant, and Chemically Modified Enzymes (∗)

The Journal of biological chemistry, 1995-03, Vol.270 (11), p.6357-6369

1995

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Fibre-type X-ray diffraction patterns from single crystals of triple helical DNA

Nature structural & molecular biology, 1994-01, Vol.1 (1), p.11-12

1994

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Synthesis and crystallographic analysis of two rhizopuspepsin inhibitor complexes

Biochemistry (Easton), 1992-09, Vol.31 (35), p.8125-8141

1992

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A new Br+ reagent. Oxidation of alcohols to carbonyl compounds by bis(quinuclidine)bromine(I) tetrafluoroborate

Journal of organic chemistry, 1986-12, Vol.51 (26), p.5454-5456

1986

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A stable bromine(+) ion complex. A twisted bicyclo[2.2.2]octane derivative. Synthesis and structure of bis(quinuclidine)bromine(I) tetrafluoroborate

Journal of the American Chemical Society, 1983-06, Vol.105 (11), p.3649-3653

1983

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Structures of complexes of rhizopuspepsin with pepstatin and other statine-containing inhibitors

Proteins, structure, function, and bioinformatics, 1992-07, Vol.13 (3), p.195-205

1992

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Crystal Structures of a Mutant (βK87T) Tryptophan Synthase α 2 β 2 Complex with Ligands Bound to the Active Sites of the α- and β-Subunits Reveal Ligand-Induced Conformational Changes

Biochemistry (Easton), 1997-06, Vol.36 (25), p.7664-7680

1997

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Exchange of K + or Cs + for Na + Induces Local and Long-Range Changes in the Three-Dimensional Structure of the Tryptophan Synthase α 2 β 2 Complex

Biochemistry (Easton), 1996-01, Vol.35 (13), p.4211-4221

1996

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What gets resident physicians stressed and how would they prefer to be supported? A best-worst scaling study

Postgraduate medical journal, 2022-12, Vol.98 (1166), p.930-935

2022

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Discovery of a Series of Pyrimidine Carboxamides as Inhibitors of Vanin‑1

Journal of medicinal chemistry, 2022-01, Vol.65 (1), p.757-784

2022

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Skin sensitization in silico protocol

Regulatory toxicology and pharmacology, 2020-10, Vol.116, p.104688-104688, Article 104688

2020

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Discovery of a Series of Efficient, Centrally Efficacious BACE1 Inhibitors through Structure-Based Drug Design

Journal of medicinal chemistry, 2015-03, Vol.58 (6), p.2678-2702

2015

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What gets resident physicians stressed and how would they prefer to be supported? A best-worst scaling study

Postgraduate medical journal, 2022-12, Vol.98 (1166), p.930

2022

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Use of Structure-Based Drug Design Approaches to Obtain Novel Anthranilic Acid Acyl Carrier Protein Synthase Inhibitors

Journal of medicinal chemistry, 2005-12, Vol.48 (25), p.7960-7969

2005

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Modeling and rendering viscous liquids

Computer animation and virtual worlds, 2004-07, Vol.15 (3-4), p.183-192

2004

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Agriculture, Trade and the Environment The Pig Sector

2003

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Convergent functional groups: synthetic and structural studies

Journal of the American Chemical Society, 1985-12, Vol.107 (25), p.7476-7481

1985

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Discovery of Fragment-Derived Small Molecules for in Vivo Inhibition of Ketohexokinase (KHK)

Discovery of PF-06835919: A Potent Inhibitor of Ketohexokinase (KHK) for the Treatment of Metabolic Disorders Driven by the Overconsumption of Fructose

Gestion durable des ressources en eau dans le secteur agricole

Crystal Structures of a Mutant (βK87T) Tryptophan Synthase α2β2 Complex with Ligands Bound to the Active Sites of the α- and β-Subunits Reveal Ligand-Induced Conformational Changes

Catalytically Active MAP KAP Kinase 2 Structures in Complex with Staurosporine and ADP Reveal Differences with the Autoinhibited Enzyme

Exchange of K+ or Cs+ for Na+ Induces Local and Long-Range Changes in the Three-Dimensional Structure of the Tryptophan Synthase α2β2 Complex

Kinetics and Mechanism of Autoprocessing of Human Immunodeficiency Virus Type 1 Protease from an Analog of the Gag-Pol Polyprotein

Ligand-mediated Changes in the Tryptophan Synthase Indole Tunnel Probed by Nile Red Fluorescence with Wild Type, Mutant, and Chemically Modified Enzymes (∗)

Fibre-type X-ray diffraction patterns from single crystals of triple helical DNA

Synthesis and crystallographic analysis of two rhizopuspepsin inhibitor complexes

A new Br+ reagent. Oxidation of alcohols to carbonyl compounds by bis(quinuclidine)bromine(I) tetrafluoroborate

A stable bromine(+) ion complex. A twisted bicyclo[2.2.2]octane derivative. Synthesis and structure of bis(quinuclidine)bromine(I) tetrafluoroborate

Structures of complexes of rhizopuspepsin with pepstatin and other statine-containing inhibitors

Crystal Structures of a Mutant (βK87T) Tryptophan Synthase α 2 β 2 Complex with Ligands Bound to the Active Sites of the α- and β-Subunits Reveal Ligand-Induced Conformational Changes

Exchange of K + or Cs + for Na + Induces Local and Long-Range Changes in the Three-Dimensional Structure of the Tryptophan Synthase α 2 β 2 Complex

What gets resident physicians stressed and how would they prefer to be supported? A best-worst scaling study

Discovery of a Series of Pyrimidine Carboxamides as Inhibitors of Vanin‑1

Utilizing Structures of CYP2D6 and BACE1 Complexes To Reduce Risk of Drug–Drug Interactions with a Novel Series of Centrally Efficacious BACE1 Inhibitors

Skin sensitization in silico protocol

Discovery of a Series of Efficient, Centrally Efficacious BACE1 Inhibitors through Structure-Based Drug Design

What gets resident physicians stressed and how would they prefer to be supported? A best-worst scaling study

Use of Structure-Based Drug Design Approaches to Obtain Novel Anthranilic Acid Acyl Carrier Protein Synthase Inhibitors

Modeling and rendering viscous liquids

Agriculture, Trade and the Environment The Pig Sector

Convergent functional groups: synthetic and structural studies

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