Adrenoceptor blocking agents. Compounds related to metoprolol
- 31 March 1981
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 24 (4) , 451-454
- https://doi.org/10.1021/jm00136a014
Abstract
A group of compounds, structurally related to metoprolol, in which the aromatic nucleus is formally moved stepwise away from the ethanolamine side chain, was studied as adrenergic agonists and antagonists in cats. All the compounds were active on the adrenergic receptors and showed similar affinity for the affinity for the receptor regardless of the distance between the aromatic nucleus and the ethanolamine moiety. An ethereal O2 may be important for the affinity to the receptor but this O2 may not necessarily have to be located as an OCH2 group between the aromatic ring and the ethanolamine chain of the .beta.-blocker molecule.This publication has 2 references indexed in Scilit:
- Synthesis and .beta.-adrenergic blocking activity of new aliphatic oxime ethersJournal of Medicinal Chemistry, 1980
- Adrenergic agents. 5. Conformational analysis of 1-alkylamino-3-aryloxy-2-propanols by proton magnetic resonance studies. Implications relating to the steric requirements of adrenoreceptorsJournal of Medicinal Chemistry, 1977