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Overview

Anthony W. Ford-Hutchinson is an independent scientist and consultant based in the United States. Their professional affiliation is categorized as an independent expert rather than being tied to a specific institution or organization.

There is no publicly available information regarding recent publications, coauthors, or a record of frequent venues in which they have published. Likewise, no specific book publications or awards have been recorded for this scientist.

Details about their main fields and subfields of study, as well as specific topics of research, have not been documented or provided in accessible records.

Given the available data, Anthony W. Ford-Hutchinson's profile reflects an individual engaged in scientific research and consulting independently within the United States. Without further detailed records, additional insights into the scope or impact of their work cannot be determined.

Best Publications

  • Identification and isolation of a membrane protein necessary for leukotriene production

    Douglas K. Miller;John W. Gillard;Philip J. Vickers;Sharon Sadowski

  • Etoricoxib (MK-0663): Preclinical Profile and Comparison with Other Agents That Selectively Inhibit Cyclooxygenase-2

    D Riendeau;M D Percival;C Brideau;S Charleson

  • The Role of Arachidonic Acid Oxygenation Products in Pain and Inflammation

    Philip Davies;Philip J. Bailey;Marvin M. Goldenberg;Anthony W. Ford-Hutchinson

  • The discovery of rofecoxib, [MK 966, VIOXX®, 4-(4′-methylsulfonylphenyl)-3-phenyl-2(5H)-furanone], an orally active cyclooxygenase-2 inhibitor

    P Prasit;Z Wang;C Brideau;C.-C Chan

  • Rofecoxib [Vioxx, MK-0966; 4-(4′-Methylsulfonylphenyl)-3-phenyl-2-(5H)-furanone]: A Potent and Orally Active Cyclooxygenase-2 Inhibitor. Pharmacological and Biochemical Profiles

    Chan Cc;Boyce S;Brideau C;Charleson S

  • Common structural features of MAPEG -- a widespread superfamily of membrane associated proteins with highly divergent functions in eicosanoid and glutathione metabolism.

    Per-Johan Jakobsson;Ralf Morgenstern;Joseph Mancini;Anthony Ford-Hutchinson

  • Biochemical and pharmacological profile of a tetrasubstituted furanone as a highly selective COX-2 inhibitor.

    D Riendeau;M D Percival;S Boyce;C Brideau

  • L-663,536 (MK-886) (3-[1-(4-chlorobenzyl)-3-t-butyl-thio-5-isopropylindol-2-yl]-2,2-dimethylpropanoic acid), a novel, orally active leukotriene biosynthesis inhibitor

    J Gillard;A W Ford-Hutchinson;C Chan;S Charleson

  • Pharmacology of a selective cyclooxygenase-2 inhibitor, L-745,337: a novel nonsteroidal anti-inflammatory agent with an ulcerogenic sparing effect in rat and nonhuman primate stomach.

    C C Chan;S Boyce;C Brideau;A W Ford-Hutchinson

  • MK886, a potent and specific leukotriene biosynthesis inhibitor blocks and reverses the membrane association of 5-lipoxygenase in ionophore-challenged leukocytes.

    C A Rouzer;A W Ford-Hutchinson;H E Morton;J W Gillard

  • Pharmacology of L-660,711 (MK-571): a novel potent and selective leukotriene D4 receptor antagonist.

    T. R. Jones;R. Zamboni;M. Belley;E. Champion

  • Pharmacology of montelukast sodium (Singulair™), a potent and selective leukotriene D4 receptor antagonist

    T R Jones;M Labelle;M Belley;E Champion

  • Identification and Characterization of a Novel Human Microsomal Glutathione S-Transferase with Leukotriene C4 Synthase Activity and Significant Sequence Identity to 5-Lipoxygenase-activating Protein and Leukotriene C4 Synthase

    Per-Johan Jakobsson;Joseph A. Mancini;Anthony W. Ford-Hutchinson

  • Membrane-associated proteins in eicosanoid and glutathione metabolism (MAPEG). A widespread protein superfamily.

    Per-Johan Jakobsson;Ralf Morgenstern;Joseph Mancini;Anthony Ford-Hutchinson

  • Identification and characterization of a novel microsomal enzyme with glutathione-dependent transferase and peroxidase activities.

    Per-Johan Jakobsson;Joseph A. Mancini;Denis Riendeau;Anthony W. Ford-Hutchinson

  • Leukotriene A3. A poor substrate but a potent inhibitor of rat and human neutrophil leukotriene A4 hydrolase.

    J F Evans;D J Nathaniel;R J Zamboni;A W Ford-Hutchinson

  • Purification to homogeneity and the N-terminal sequence of human leukotriene C4 synthase: a homodimeric glutathione S-transferase composed of 18-kDa subunits.

    Donald W. Nicholson;Ambereen Ali;John P. Vaillancourt;Jimmy R. Calaycay

  • Pharmacology of MK-0591 (3-[1-(4-chlorobenzyl)-3-(t-butylthio)-5-(quinolin-2-yl-methoxy)- indol-2-yl]-2,2-dimethyl propanoic acid), a potent, orally active leukotriene biosynthesis inhibitor.

    Christine Brideau;Chi-Chung Chan;S. Charleson;Deschenes Denis

  • Discovery of MK-0476, a potent and orally active leukotriene D4 receptor antagonist devoid of peroxisomal enxyme induction

    M. Labelle;M. Belley;Y. Gareau;J.Y. Gauthier

  • FLAP : A NOVEL DRUG TARGET FOR INHIBITING THE SYNTHESIS OF LEUKOTRIENES

    Anthony W. Ford-Hutchinson

Frequent Co-Authors

Robert Zamboni
Robert Zamboni MSD (United States)
Robert N. Young
Robert N. Young Simon Fraser University
Joseph A. Mancini
Joseph A. Mancini MSD (United States)
Donald W. Nicholson
Donald W. Nicholson MSD (United States)
Joshua Rokach
Joshua Rokach Florida Institute of Technology
Denis Riendeau
Denis Riendeau MSD (United States)
Brian P. Kennedy
Brian P. Kennedy MSD (United States)
Ralf Morgenstern
Ralf Morgenstern Karolinska Institute
Bengt Samuelsson
Bengt Samuelsson Karolinska Institute
Hans Bisgaard
Hans Bisgaard University of Copenhagen

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