Synthesis and serotonin receptor activity of the arylpiperazine alkyl/propoxy derivatives of new azatricycloundecanes
A set of 36 arylpiperazine derivatives with two novel complex terminal imide fragments, 8,11-dimethyl-3,5-dioxo-4-azatricyclo[5.2.2.0 2,6]undec-8-en-1-yl acetate and 1,11-dimethyl-4-azatricyclo[5.2.2.0 2,6]undecane-3,5,8-trione, were synthesized and tested for their affinity for 5-HT 1A and 5-HT 2A...
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Published in | European journal of medicinal chemistry Vol. 44; no. 1; pp. 152 - 164 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
ISSY-LES-MOULINEAUX
Elsevier Masson SAS
2009
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | A set of 36 arylpiperazine derivatives with two novel complex terminal imide fragments, 8,11-dimethyl-3,5-dioxo-4-azatricyclo[5.2.2.0
2,6]undec-8-en-1-yl acetate and 1,11-dimethyl-4-azatricyclo[5.2.2.0
2,6]undecane-3,5,8-trione, were synthesized and tested for their affinity for 5-HT
1A and 5-HT
2A receptors. The Fujita–Ban analysis showed that the influence of structural modifications on the affinity for both receptor subtypes is additive and that the activity of similar compounds could be predicted with high accuracy. Compounds
46,
48 and
18 out of 14 screened in a functional model of anxiety and depression demonstrated antidepressant activity in the forced swimming tests in mice, and were devoid of neurotoxic effects (chimney test in mice).
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ISSN: | 0223-5234 1768-3254 |
DOI: | 10.1016/j.ejmech.2008.03.019 |