Search Results - "Dack, K."

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  1. 1

    COVID-19 associated with universities in England, October 2020–February 2022 by Dack, K., Wilson, A., Turner, C., Anderson, C., Hughes, G.J.

    Published in Public health (London) (01-11-2023)
    “…The aim of this study was to describe the epidemiology of COVID-19 cases at universities in England (October 2020–February 2022) and investigate factors…”
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    Journal Article
  2. 2

    In vitro and in vivo characterization of PF‐04418948, a novel, potent and selective prostaglandin EP 2 receptor antagonist by af Forselles, KJ, Root, J, Clarke, T, Davey, D, Aughton, K, Dack, K, Pullen, N

    Published in British journal of pharmacology (01-12-2011)
    “…BACKGROUND AND PURPOSE Studies of the role of the prostaglandin EP 2 receptor) have been limited by the availability of potent and selective antagonist tools…”
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    In vitro and in vivo characterization of PF‐04418948, a novel, potent and selective prostaglandin EP2 receptor antagonist by af Forselles, KJ, Root, J, Clarke, T, Davey, D, Aughton, K, Dack, K, Pullen, N

    Published in British journal of pharmacology (01-12-2011)
    “…BACKGROUND AND PURPOSE Studies of the role of the prostaglandin EP2 receptor) have been limited by the availability of potent and selective antagonist tools…”
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    Journal Article
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    Thromboxane Modulating Agents. 3. 1H-Imidazol-1-ylalkyl- and 3-Pyridinylalkyl-Substituted 3-[2-[(Arylsulfonyl)amino]ethyl]benzenepropanoic Acid Derivatives as Dual Thromboxane Synthase Inhibitor/Thromboxane Receptor Antagonists by Dickinson, Roger P, Dack, Kevin N, Long, Clive J, Steele, John

    Published in Journal of medicinal chemistry (10-10-1997)
    “…The design of a series of dual thromboxane synthase inhibitor/thromboxane receptor antagonists based on a 3-[2-[(arylsulfonyl)amino]ethyl]benzenepropanoic acid…”
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  8. 8

    Thromboxane modulating agents. 4. Design and synthesis of 3-(2-[{(4-chlorophenyl)sulfonyl}amino]ethyl)benzenepropanoic acid derivatives as potent thromboxane receptor antagonists by Dack, Kevin N., Dickinson, Roger P., Long, Clive J., Steele, John

    Published in Bioorganic & medicinal chemistry letters (18-08-1998)
    “…The design of a series of thromboxane receptor antagonists based on 3-(2-[{(4-chlorophenyl)sulfonyl}amino]ethyl)benzenepropanoic acid ( 1) is described…”
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    Journal Article
  9. 9

    Design of ester prodrugs to enhance oral absorption of poorly permeable compounds: challenges to the discovery scientist by Beaumont, Kevin, Webster, Robert, Gardner, Iain, Dack, Kevin

    Published in Current drug metabolism (01-12-2003)
    “…Many drugs are administered at sites that are remote from their site of action. The most common route of drug delivery is the oral route. The optimal…”
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    Journal Article
  10. 10

    Absorption, Distribution, Metabolism, and Excretion Considerations in Selection of Orally Active Indole-Containing Endothelin Antagonist by WALKER, Donald K, DACK, Kevin N, DICKINSON, Roger P, FENNER, Katherine S, JAMES, Kim, RAWSON, David J, SMITH, Dennis A

    Published in Drug metabolism and disposition (01-11-2001)
    “…A series of potent indole-containing endothelin antagonists were evaluated in rat pharmacokinetic studies as part of a rational drug design program. Early…”
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    Thromboxane modulating agents. 1. Design of 1-[(arylsulfonyl)amino] alkylindole derivatives as dual thromboxane synthase inhibitor/thromboxane receptor antagonists by Dickinson, Roger P., Dack, Kevin N., Steele, John

    Published in Bioorganic & medicinal chemistry letters (21-12-1995)
    “…The design of a series of dual thromboxane synthase inhibitor/thromboxane receptor antagonists based on an indole thromboxane synthase inhibitor template is…”
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  15. 15

    Thromboxane modulating agents. 2. Thromboxane receptor antagonists derived from the thromboxane synthase inhibitor dazmegrel by Dickinson, Roger P., Dack, Kevin N., Steele, John, Tute, Michael S.

    Published in Bioorganic & medicinal chemistry letters (23-07-1996)
    “…The design of dual thromboxane synthase inhibitor/thromboxane receptor antagonists (e.g. 15) based on the structure of the thromboxane synthase inhibitor…”
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    Journal Article