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There is no page with the exact title "Pharmacokinetic". The search results for "Pharmacokinetic" are displayed below. You can create a page titled Pharmacokinetic (by clicking on the red link).

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Article title matches

  1. Category:Pharmacokinetic (46 bytes)
    1: List of pages with the keyword Pharmacokinetic
  2. Category:Pharmacokinetic property (55 bytes)
    1: List of pages with the keyword Pharmacokinetic property
  3. Category:Pharmacokinetic sensor (53 bytes)
    1: List of pages with the keyword Pharmacokinetic sensor

Page text matches

  1. 2j94 (5,654 bytes)
    26: ...rved within this series of potent fXa inhibitors. Pharmacokinetic profiles in rat and dog, together with selectivit...
  2. 2j95 (5,600 bytes)
    26: ...rved within this series of potent fXa inhibitors. Pharmacokinetic profiles in rat and dog, together with selectivit...
  3. 1h1b (6,554 bytes)
    26: ...ibitors, with a prolonged pharmacodynamic action. Pharmacokinetically, these compounds are comparable with 1 while ...
  4. 2jc1 (9,028 bytes)
    24: ...ubmicromolar potency in the HCV replicon and good pharmacokinetic properties.
  5. 2jc0 (9,030 bytes)
    24: ...ubmicromolar potency in the HCV replicon and good pharmacokinetic properties.
  6. 2uzw (7,305 bytes)
    24: ...improved cardiovascular safety profile. The SARs, pharmacokinetic profile, and CV safety of selected Akt inhibitors...
  7. 2uzt (7,322 bytes)
    24: ...improved cardiovascular safety profile. The SARs, pharmacokinetic profile, and CV safety of selected Akt inhibitors...
  8. 2uzu (7,340 bytes)
    24: ...improved cardiovascular safety profile. The SARs, pharmacokinetic profile, and CV safety of selected Akt inhibitors...
  9. 2uzv (5,295 bytes)
    24: ...improved cardiovascular safety profile. The SARs, pharmacokinetic profile, and CV safety of selected Akt inhibitors...
  10. 2j14 (4,553 bytes)
    24: ...nvestigated and optimized for a favorable in vivo pharmacokinetic profile. Isoxazole LCI765 (17d) was found to be a...
  11. 2j50 (5,903 bytes)
    24: ...cancer cell lines, favorable chemico-physical and pharmacokinetic properties, and high efficacy in in vivo tumor mo...
  12. 1w5w (11,987 bytes)
    24: ...e development of potent inhibitors with different pharmacokinetic profiles towards resistant protease mutants.
  13. 1w5y (11,987 bytes)
    24: ...e development of potent inhibitors with different pharmacokinetic profiles towards resistant protease mutants.
  14. 1w5x (11,987 bytes)
    24: ...e development of potent inhibitors with different pharmacokinetic profiles towards resistant protease mutants.
  15. 1w5v (11,924 bytes)
    24: ...e development of potent inhibitors with different pharmacokinetic profiles towards resistant protease mutants.
  16. 1uom (6,986 bytes)
    24: ...fect of N-phenyl substituents on the activity and pharmacokinetic properties of tetrahydroisoquinoline analogues wa...
  17. 2bm2 (5,402 bytes)
    24: ...change of the benzamidine to optimize potency and pharmacokinetic properties gave selective, potent and orally bioa...
  18. 2bhj (4,257 bytes)
    24: ...wo compounds (16 and 30) demonstrate a reasonable pharmacokinetic profile in rodents. The synthesis, SAR, and biolo...
  19. 4j3j (5,239 bytes)
    14: ...e performed on this series, revealing undesirable pharmacokinetic profiles for the triazole compounds. To overcome ...
  20. 2j4z (5,883 bytes)
    24: ...cancer cell lines, favorable chemico-physical and pharmacokinetic properties, and high efficacy in in vivo tumor mo...

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