Pharmacokinetics Parameters.

<p>For the two compounds whose pharmacokinetics is described by Eqs <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0133653#pone.0133653.e004" target="_blank">3</a> and <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0133653#pone.0133653.e005" target="_blank">4</a>, the table lists the respective PK parameters: partition coefficients <i>κ</i>, permeabilities <i>P</i>, metabolization parameters </p><p></p><p></p><p></p><p><mi>V</mi>maxcell</p><p></p><p></p><p></p> and <p></p><p></p><p></p><p><mi>K</mi><mi>m</mi>cell</p><p></p><p></p><p></p>; the lipophilicity log <i>P</i><p>