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A novel series of N-(hexahydro-1,4-diazepin-6-yl) and N-(hexahydroazepin- 3-yl)benzamides with high affinity for 5-HT3 and dopamine D2 receptors.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 1998 Mar 17; Vol. 8 (6), pp. 619-24. - Publication Year :
- 1998
-
Abstract
- A novel series of benzamides with a hexahydro-1,4-diazepine or hexahydroazepine ring in the amine moiety were prepared, and their binding affinities for 5-HT3 and dopamine D2 receptors were evaluated. The R isomer of the 1-ethyl-4-methylhexahydro-1,4-diazepinylbenzamide (R)-22 had potent affinity for both receptors. The R-enantiomer of the corresponding 1-ethylhexahydroazepinylbenzamide 28 showed potent affinity for dopamine D2 receptors with reduced affinity for 5-HT3 receptors, while the S isomer was found to be a potent and selective 5-HT3 receptor antagonist.
- Subjects :
- Animals
Binding Sites
Cerebral Cortex metabolism
Corpus Striatum metabolism
Domperidone metabolism
Dopamine Antagonists metabolism
Imidazoles metabolism
Indoles metabolism
Ligands
Metoclopramide metabolism
Models, Chemical
Ondansetron metabolism
Rats
Receptors, Serotonin, 5-HT3
Serotonin Antagonists metabolism
Spiperone metabolism
Stereoisomerism
Benzamides metabolism
Receptors, Dopamine D2 metabolism
Receptors, Serotonin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0960-894X
- Volume :
- 8
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 9871571
- Full Text :
- https://doi.org/10.1016/s0960-894x(98)00078-x