The displacement of [3H]SCH-23390 and of [3H]spiperone from striatal, dopamine D1- and D2-type receptors by several quinolizidinyl-derivatives of bi- and tricyclic systems was investigated. All tested compounds did not affect SCH-23390 binding and exhibited only weak activity on spiperone binding to D2 binding sites (Ki = 1.9 microM). Therefore the good deconditioning activity (CAR blockade in rats) of 6-chloro-1-lupinyl-3-methyl-quinoxalinone (18) must rely on interactions with other kinds of receptors.

Poor interaction of some quinolizidine derivatives with dopamine D1- and D2- type receptors / A. Sparatore, A. Vaccari, V. Boido, F. Spartore. - In: IL FARMACO. - ISSN 0014-827X. - 50:3(1995 Mar), pp. 217-219.

Poor interaction of some quinolizidine derivatives with dopamine D1- and D2- type receptors

A. Sparatore
Primo
;
1995

Abstract

The displacement of [3H]SCH-23390 and of [3H]spiperone from striatal, dopamine D1- and D2-type receptors by several quinolizidinyl-derivatives of bi- and tricyclic systems was investigated. All tested compounds did not affect SCH-23390 binding and exhibited only weak activity on spiperone binding to D2 binding sites (Ki = 1.9 microM). Therefore the good deconditioning activity (CAR blockade in rats) of 6-chloro-1-lupinyl-3-methyl-quinoxalinone (18) must rely on interactions with other kinds of receptors.
Rats; Animals; Receptors, Dopamine D2; Receptors, Dopamine D1; Benzazepines; Neostriatum; Binding, Competitive; Quinolizines; Spiperone
Settore CHIM/08 - Chimica Farmaceutica
mar-1995
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/183950
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