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Selective Inhibitors of Monoamine Oxidase. 3. Structure−Activity Relationship of Tricyclics Bearing Imidazoline, Oxadiazole, or Tetrazole Groups
- Source :
- Journal of Medicinal Chemistry. 39:1857-1863
- Publication Year :
- 1996
- Publisher :
- American Chemical Society (ACS), 1996.
-
Abstract
- Inhibition of monoamine oxidase A (MAO A) is believed to cause antidepressant and possibly antianxiety effects. The previous paper had developed structure-activity relationships (SAR) for in vitro MAO A inhibition by tricyclic N-arylamides. It is shown in this paper that the same in vitro SAR can be carried over to tricyclics whose potentially toxic amide function is replaced by an appropriately substituted imidazoline, a 1,2,4- or 1,3,4-oxadiazole, or an alkylated tetrazole moiety. Dialysis of the inhibitor from the enzyme was used as a measure of reversibility which correlates with a low ability to cause a blood pressure rise with ingested tyramine ("cheese effect").
- Subjects :
- Oxadiazoles
Monoamine Oxidase Inhibitors
biology
Monoamine oxidase
Stereochemistry
fungi
Imidazoles
Tetrazoles
Oxadiazole
Imidazoline receptor
body regions
Structure-Activity Relationship
chemistry.chemical_compound
chemistry
Drug Discovery
biology.protein
Molecular Medicine
Antidepressant
Structure–activity relationship
Tetrazole
Monoamine oxidase A
skin and connective tissue diseases
Subjects
Details
- ISSN :
- 15204804 and 00222623
- Volume :
- 39
- Database :
- OpenAIRE
- Journal :
- Journal of Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....925bc5b5016fbf3f18f847d272c34fc5