Search Results - "Beaumont, K C"

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  1. 1

    Pharmacokinetics and metabolism of darifenacin in the mouse, rat, dog and man by BEAUMONT, K. C., CUSSANS, N. J., NICHOLS, D. J., SMITH, D. A.

    Published in Xenobiotica (1998)
    “…1. Followingintravenousadministrationto animals at 2 5 mg kg, darifenacinexhibited terminal plasma half-lifes < 2 h due to high plasma clearance (with respect…”
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    Journal Article
  2. 2

    Potential role for P-glycoprotein in the nonproportional pharmacokinetics of UK-343,664 in man by Abel, S., Beaumont, K. C., Crespi, C. L., Eva, M. D., Fox, L., Hyland, R., Jones, B. C., Muirhead, G. J., Smith, D. A., Venn, R. F., Walker, D. K.

    Published in Xenobiotica (01-01-2001)
    “…1. UK-343,664 is a potent and specific PDE5 inhibitor. Following single oral doses to human volunteers, it exhibited non-proportional pharmacokinetics over the…”
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    Journal Article
  3. 3

    Pharmacokinetics and metabolism of zamifenacin in mouse, rat, dog and man by Beaumont, K C, Causey, A G, Coates, P E, Smith, D A

    Published in Xenobiotica (01-04-1996)
    “…1. Zamifenacin was rapidly metabolized in vitro by liver microsomes from rat, dog, and man. 2. Zamifenacin exhibited extensive plasma protein binding with…”
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    Journal Article
  4. 4

    Pharmacokinetics and metabolism of a selective PDE5 inhibitor (UK-343,664) in rat and dog by Walker, D. K., Beaumont, K. C., Comby, P., Evans, K. M., Gedge, J. I., Halliday, R. C., Roffey, S. J., Wright, P. A.

    Published in Xenobiotica (01-08-2001)
    “…1. UK-343,664 is a novel potent and selective PDE5 inhibitor. Plasma clearances in the male and female rat were high (120 and 54 ml min-1 kg-1), giving rise to…”
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    Journal Article
  5. 5

    Pharmacokinetics of a series of bis(methanesulphonamido-arylalkyl)amines in the beagle dog by Walker, D K, Beaumont, K C, Stopher, D A, Smith, D A

    Published in Xenobiotica (01-10-1996)
    “…1. The pharmacokinetics of three closely related analogues of dofetilide have been investigated in the beagle dog. These have been compared with those of…”
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  6. 6

    Potential role for P-glycoprotein in the non-proportional pharmacokinetics of UK-343,664 in man by Abel, S, Beaumont, K C, Crespi, C L, Eve, M D, Fox, L, Hyland, R, Jones, B C, Muirhead, G J, Smith, D A, Venn, R F, Walker, D K

    Published in Xenobiotica (01-08-2001)
    “…1. UK-343,664 is a potent and specific PDE5 inhibitor. Following single oral doses to human volunteers, it exhibited non-proportional pharmacokinetics over the…”
    Get full text
    Journal Article
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