Literature DB >> 6694167

Conformationally restricted congeners of dopamine derived from octahydrobenzo[g]quinoline and octahydrobenzo[f]quinoline.

J G Cannon, R L Hamer, M Ilhan, R K Bhatnagar, J P Long.   

Abstract

Series of N-alkylated derivatives of trans-octahydrobenzo[g]quinoline and of cis- and trans-octahydrobenzo[f]quinoline were prepared for pharmacological testing as congeners of 2-amino-5,7-dihydroxytetralin, which elicits dopaminergic effects in a variety of assays. Trans-fused compounds bearing N-ethyl or N-n-propyl displayed high potency/activity in inhibition of effect of stimulation of the cat cardioaccelerator nerve. Certain N-alkyl homologues in the octahydrobenzo[f]quinoline series showed high potency in binding studies in rat caudate homogenate.

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Year:  1984        PMID: 6694167     DOI: 10.1021/jm00368a015

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

1.  Structurally constrained hybrid derivatives containing octahydrobenzo[g or f]quinoline moieties for dopamine D2 and D3 receptors: binding characterization at D2/D3 receptors and elucidation of a pharmacophore model.

Authors:  Dennis A Brown; Prashant S Kharkar; Ingrid Parrington; Maarten E A Reith; Aloke K Dutta
Journal:  J Med Chem       Date:  2008-12-25       Impact factor: 7.446

2.  Synthesis, Structure Activity Relationship Studies and Pharmacological Evaluation of 2-Phenyl-3-(Substituted Phenyl)-3H-Quinazolin-4-ones as Serotonin 5-HT(2) Antagonists.

Authors:  N Sati; S Kumar; M S M Rawat
Journal:  Indian J Pharm Sci       Date:  2009-09       Impact factor: 0.975

  2 in total

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