.alpha.-Adrenoceptor reagents. 2. Effects of modification of the 1,4-benzodioxan ring system on .alpha.-adrenoreceptor activity

Journal of Medicinal Chemistry
1984.0

Abstract

Modification of the 1,4-benzodioxan ring present in RX 781094 has not previously been considered. This paper describes a number of analogues of this ring system, including compounds in which one of the oxygen atoms has been replaced by a methylene group and also those in which the ring size has been changed to give, for example, furan and thiophene derivatives. The dihydrobenzofuranylimidazoline compound 7 is the only analogue possessing presynaptic antagonist potency potency and selectivity comparable to that of 1. In view of this result, a number of derivatives was prepared to determine the structure-activity relationships within this series. Many derivatives, as well as the parent compound 7, were found to possess presynaptic alpha 2-adrenoreceptor antagonist and postsynaptic alpha 1-adrenoreceptor partial agonist properties. Two of the selective presynaptic antagonists, 13 and 14 possess greater potency and selectivity than that possessed by 1. The 5-chloro derivative 25 is twice as potent as after oral administration but only about half as potent when given intravenously.

Knowledge Graph

Similar Paper

.alpha.-Adrenoceptor reagents. 2. Effects of modification of the 1,4-benzodioxan ring system on .alpha.-adrenoreceptor activity
Journal of Medicinal Chemistry 1984.0
.alpha.-Adrenoreceptor reagents. 1. Synthesis of some 1,4-benzodioxans as selective presynaptic .alpha.2-adrenoreceptor antagonists and potential antidepressants
Journal of Medicinal Chemistry 1983.0
Indoline analogs of idazoxan: potent .alpha.2-antagonists and .alpha.1-agonists
Journal of Medicinal Chemistry 1988.0
Effect of methoxy substitution on the adrenergic activity of three structurally related .alpha.2-adrenoreceptor antagonists
Journal of Medicinal Chemistry 1986.0
Structure−Activity Relationships in 1,4-Benzodioxan-Related Compounds. 6. Role of the Dioxane Unit on Selectivity for α<sub>1</sub>-Adrenoreceptor Subtypes
Journal of Medicinal Chemistry 1999.0
2,4-Diamino-6,7-dimethoxyquinazolines. 1. 2-[4-(1,4-Benzodioxan-2-ylcarbonyl)piperazin-1-yl] derivatives as .alpha.1-adrenoceptor antagonists and antihypertensive agents
Journal of Medicinal Chemistry 1987.0
2-[[[2-(2,6-Dimethoxyphenoxy)ethyl]amino]methyl]-1,4-benzoxathian: a new antagonist with high potency and selectivity towards .alpha.1-adrenoreceptors
Journal of Medicinal Chemistry 1984.0
Structure−Activity Relationships in 1,4-Benzodioxan-Related Compounds. 9. From 1,4-Benzodioxane to 1,4-Dioxane Ring as a Promising Template of Novel α<sub>1D</sub>-Adrenoreceptor Antagonists, 5-HT<sub>1A</sub>Full Agonists, and Cytotoxic Agents
Journal of Medicinal Chemistry 2008.0
Structure-activity relationships for 2-substituted imidazoles as .alpha.2-adrenoceptor antagonists
Journal of Medicinal Chemistry 1982.0
New Substituted 1-(2,3-Dihydrobenzo[1,4]dioxin-2-ylmethyl)piperidin-4-yl Derivatives with α<sub>2</sub>-Adrenoceptor Antagonist Activity
Journal of Medicinal Chemistry 2000.0