Studies toward the discovery of the next generation of antidepressants. Part 6: Dual 5-HT1A receptor and serotonin transporter affinity within a class of arylpiperazinyl-cyclohexyl indole derivatives

Based on the previously reported discovery lead, 3-(cis-4-(4-(1H-indol-4-yl)piperazin-1-yl)cyclohexyl)-5-fluoro-1H-indole (2), a series of related arylpiperazin-4-yl-cyclohexyl indole analogs were synthesized then evaluated as 5-HT transporter inhibitors and 5-HT(1A) receptor antagonists. The invest...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2008-07, Vol.16 (14), p.6707-6723
Hauptverfasser: DAHUI ZHOU, PING ZHOU, SMITH, Deborah L, ANDREE, Terrance H, MEWSHAW, Richard E, EVRARD, Deborah A, MEAGHER, Kristin, WEBB, Michael, HARRISON, Boyd L, HURYN, Donna M, GOLEMBIESKI, Jeannette, HOMBY, Geoffrey A, SCHECHTER, Lee E
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Sprache:eng
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Zusammenfassung:Based on the previously reported discovery lead, 3-(cis-4-(4-(1H-indol-4-yl)piperazin-1-yl)cyclohexyl)-5-fluoro-1H-indole (2), a series of related arylpiperazin-4-yl-cyclohexyl indole analogs were synthesized then evaluated as 5-HT transporter inhibitors and 5-HT(1A) receptor antagonists. The investigation of the structure-activity relationships revealed the optimal pharmacophoric elements required for activities in this series. The best example from this study, 5-(piperazin-1-yl)quinoline analog (trans-20), exhibited equal binding affinities at 5-HT transporter (K(i)=4.9nM), 5-HT(1A) receptor (K(i)=6.2nM) and functioned as a 5-HT(1A) receptor antagonist.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2008.05.075