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PMID: 6796690 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

3-Phenylpiperidines. Central dopamine-autoreceptor stimulating activity.

Journal of medicinal chemistry ·Vol. 24 ·No. 12 ·1981-12-00 ·Pages 1475-82

Hacksell U, Arvidsson LE, Svensson U, Nilsson JL, Sanchez D, Wikström H, Lindberg P, Hjorth S, Carlsson A

Abstract

Thirty compounds related to the selective dopamine-autoreceptor agonist 3-(3-hydroxyphenyl)-N-n-propylpiperidine have been synthesized and tested for central dopamine-autoreceptor stimulating activity. The 3-(3-hydroxyphenyl)piperidine moiety seems indispensable for high potency and selectivity. Introduction of an additional hydroxyl group into the 4 position of the aromatic ring gives a compound with dopaminergic activity but lacking selectivity for autoreceptors. 3-(3-Hydroxyphenyl)-N-n-propylpyrrolidine, 3-(3-hydroxy)-N-n-propylperhydroazepine, and 3-(3-hydroxyphenyl)quinuclidine were all inactive. The most potent compounds were the N-isopropyl-, N-n-butyl-, N-n-pentyl-, and N-phenethyl-substituted 3-(3-hydroxyphenyl)piperidine derivatives. None of the compounds investigated seemed to have central noradrenaline- or serotonin-receptor stimulating activity.

MeSH Terms
5-Hydroxytryptophan/metabolism Animals Apomorphine/pharmacology Central Nervous System/drug effects Chemical Phenomena Chemistry Dihydroxyphenylalanine/metabolism Drug Interactions Male Motor Activity/drug effects Neurons/drug effects Piperidines/chemical synthesis,pharmacology Rats Rats, Inbred Strains Receptors, Dopamine/drug effects Stimulation, Chemical
Chemicals
Piperidines Receptors, Dopamine Dihydroxyphenylalanine 5-Hydroxytryptophan Apomorphine
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Hacksell U
Arvidsson L E
Svensson U
Nilsson J L
Sanchez D
Wikström H
Lindberg P
Hjorth S
Carlsson A
Article Info
Journal
Journal of medicinal chemistry
Abbr.
J Med Chem
ISSN
0022-2623
Published
1981-12-00
Pages
1475-82
Language
English
Region
United States
NLM ID
9716531
Subset
IM
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