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<p>and <a href="page.php?w=area-under-the-curve_%28pharmacokinetics%29">total exposure</a> of zolmitriptan and its <a href="page.php?w=active_metabolite">active metabolite</a> were approximately doubled. The major <a href="page.php?w=metabolite">metabolite</a> of zolmitriptan, N-desmethylzolmitriptan (183C91), which is active and has several-fold greater <a href="page.php?w=affinity_%28pharmacology%29">affinity</a> for the <a href="page.php?w=serotonin">serotonin</a> <a href="page.php?w=5-HT1B_receptor">5-HT<sub>1B</sub></a> and <a href="page.php?w=5-HT1D_receptor">5-HT<sub>1D</sub> receptor</a>s</p><p>
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