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  2. Lisinopril - Wikipedia

    en.wikipedia.org/wiki/Lisinopril

    Lisinopril leaves the body completely unchanged in the urine. [1] [16] The half-life of lisinopril is 12 hours, and is increased in people with kidney problems. [1] [16] While the plasma half-life of lisinopril has been estimated between 12 and 13 hours, the elimination half-life is much longer, at around 30 hours. [18]

  3. Lipinski's rule of five - Wikipedia

    en.wikipedia.org/wiki/Lipinski's_Rule_of_Five

    Lipinski's rule of five, also known as Pfizer's rule of five or simply the rule of five (RO5), is a rule of thumb to evaluate druglikeness or determine if a chemical compound with a certain pharmacological or biological activity has chemical properties and physical properties that would likely make it an orally active drug in humans.

  4. File:Lisinopril Structural Formulae V.2.svg - Wikipedia

    en.wikipedia.org/wiki/File:Lisinopril_Structural...

    The following other wikis use this file: Usage on ar.wikipedia.org ليزينوبريل; Usage on de.wikipedia.org Lisinopril; Usage on es.wikipedia.org

  5. Physiologically based pharmacokinetic modelling - Wikipedia

    en.wikipedia.org/wiki/Physiologically_based...

    The absorption of a chemical deposited on skin can also be modeled using first order terms. It is best in that case to separate the skin from the other tissues, to further differentiate exposed skin and non-exposed skin, and differentiate viable skin (dermis and epidermis) from the stratum corneum (the actual skin upper layer exposed).

  6. File:Lisinopril.svg - Wikipedia

    en.wikipedia.org/wiki/File:Lisinopril.svg

    The following other wikis use this file: Usage on de.wikibooks.org Pharmakologie und Toxikologie: Herz-Kreislauf; Usage on fi.wikipedia.org Käyttäjä:Nitraus/A

  7. File:Lisinopril structure.svg - Wikipedia

    en.wikipedia.org/wiki/File:Lisinopril_structure.svg

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  8. Distribution (pharmacology) - Wikipedia

    en.wikipedia.org/wiki/Distribution_(pharmacology)

    Distribution in pharmacology is a branch of pharmacokinetics which describes the reversible transfer of a drug from one location to another within the body.. Once a drug enters into systemic circulation by absorption or direct administration, it must be distributed into interstitial and intracellular fluids.

  9. Pharmacokinetics - Wikipedia

    en.wikipedia.org/wiki/Pharmacokinetics

    That is, the closer time points are, the closer the trapezoids reflect the actual shape of the concentration-time curve. The number of time points available in order to perform a successful NCA analysis should be enough to cover the absorption, distribution and elimination phase to accurately characterize the drug.