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- W1987112069 abstract "Abstract Several 1-aryl-4-(2-arylethyl)piperazine derivatives were synthesized and tested in-vitro for their binding affinity for 5-HT7 and 5-HT1A receptors. These compounds displayed 5-HT7 receptor affinity ranging between Ki = 474 nm and Ki = 8.2 nm, besides high affinity for the 5-HT1A receptor. Intrinsic activity of the most potent compounds was assessed. 4-[2-(3-Methoxyphenyl)ethyl]-1-(2-methoxyphenyl)piperazine (16) and 1-(1,2-benzisoxazol-3-yl)-4-[2-(3-methoxyphenyl)ethyl]piperazine (20) (Ki = 24.5 and 8.2 nm, respectively) behaved as partial agonist and full agonist, respectively, when tested for 5-HT7 receptor-mediated relaxation of substance P-induced guinea-pig ileum contraction." @default.
- W1987112069 created "2016-06-24" @default.
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- W1987112069 date "2004-02-01" @default.
- W1987112069 modified "2023-10-16" @default.
- W1987112069 title "Studies on 1-arylpiperazine derivatives with affinity for rat 5-HT7 and 5-HT1A receptors" @default.
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- W1987112069 doi "https://doi.org/10.1211/0022357022575" @default.
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