Studies on a series of potent, orally bioavailable, 5-HT1 receptor ligands-Part II

2007 
A series of 5-( piperidinylethyloxy) quinoline 5-HT1 receptor ligands have been studied by elaboration of the series of dual 5-HT1-SSRIs reported previously. These new compounds display a different in vitro pharmacological pro. le with potent affinity across the 5-HT1A, 5-HT1B and 5-HT1D receptors and selectivity against the serotonin transporter. Furthermore, they have improved pharmacokinetic profiles and CNS penetration.
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