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Structure-activity relationship studies of CNS agents. Part 14: Structural requirements for the 5-HT1A and 5-HT2A receptor selectivity of simple 1-(2-pyrimidinyl)piperazine derivatives.
- Source :
-
Die Pharmazie [Pharmazie] 1994 Nov; Vol. 49 (11), pp. 801-6. - Publication Year :
- 1994
-
Abstract
- The 5-HT1A and 5-HT2A receptor affinity of model 1-(2-pyrimidinyl)-piperazine derivatives 15-21 and 23-32 has been determined. 2-(N-Methylpiperazino)-4,6-di(2-thienyl)pyrimidine 26 is a new, highly active and selective 5-HT2A receptor ligand. The topography of a molecule and the stereoelectronic effects of the thiophene rings are the major factors responsible for the high affinity and selectivity of 26 towards 5-HT2A sites.
- Subjects :
- Alkylation
Animals
Central Nervous System Agents pharmacology
Models, Molecular
Piperazines pharmacology
Radioligand Assay
Rats
Serotonin Antagonists pharmacology
Structure-Activity Relationship
Central Nervous System Agents chemical synthesis
Piperazines chemical synthesis
Receptors, Serotonin drug effects
Serotonin Antagonists chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 0031-7144
- Volume :
- 49
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Die Pharmazie
- Publication Type :
- Academic Journal
- Accession number :
- 7838864