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Selective Inhibitors of Monoamine Oxidase. 3. Structure−Activity Relationship of Tricyclics Bearing Imidazoline, Oxadiazole, or Tetrazole Groups

Authors :
Darryl J. Heuser
Charles T. Joyner
Batchelor John F
Morton Harfenist
Helen L. White
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").

Details

ISSN :
15204804 and 00222623
Volume :
39
Database :
OpenAIRE
Journal :
Journal of Medicinal Chemistry
Accession number :
edsair.doi.dedup.....925bc5b5016fbf3f18f847d272c34fc5