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<p>and <a href="page.php?w=vasopressin">vasopressin</a>.</p>

<p><big>Pharmacokinetics</big></p>
<p>When administered orally, CBN demonstrates a similar metabolism to ?<sup>9</sup>-THC, with the primary intoxicating metabolite being produced through a <a href="page.php?w=hydroxylation">hydroxylation</a> reaction that occurs in the liver. The active metabolite generated via this process is called <a href="page.php?w=11-Hydroxycannabinol">11-OH-CBN</a>, which is around two times as potent as CBN, and has demonstrated activity as a weak CB2 <a href="page.php?w=Receptor_antagonist">antagonist</a>.</p><p>
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