Synthesis and structure-activity relationships of new arylpiperazines: para substitution with electron-withdrawing groups decrease binding to 5-HT(1A) and D(2A) receptors.

Santana, Lourdes

Synthesis and structure-activity relationships of new arylpiperazines: para substitution with electron-withdrawing groups decrease binding to 5-HT(1A) and D(2A) receptors. [electronic resource] - European journal of medicinal chemistry Jun 2002 - 503-10 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0223-5234

10.1016/s0223-5234(02)01357-0 doi


8-Hydroxy-2-(di-n-propylamino)tetralin--pharmacology
Animals
Coumarins--chemical synthesis
Drug Design
Electrons
Fibroblasts
Hippocampus--drug effects
Humans
In Vitro Techniques
Indicators and Reagents
Mice
Piperazines--chemical synthesis
Raclopride--pharmacology
Radioligand Assay
Rats
Rats, Sprague-Dawley
Receptors, Dopamine D2--drug effects
Receptors, Serotonin--drug effects
Receptors, Serotonin, 5-HT1
Structure-Activity Relationship