Abstract
In this study, 12 new 2,2,7,7-tetramethyl-9-aryl-2,3,4,5,6,7,9,10-octahydro-1,8-acridindione derivatives were synthesised and their effects on vascular potassium channels and mechanism of induced relaxations on phenylephrine-induced contractile responses in isolated rabbit thoracic arteries was investigated. Pinacidil was used as standard potassium channel openers in this study. Compounds 1-12 and pinacidil exerted concentration-dependent relaxation responses precontracted phenylephrine in the aortic rings with the efficacy order: 11>pinacidil>7>2>8>3>1>4>10>6>9>5>12.
| Original language | English |
|---|---|
| Pages (from-to) | 519-523 |
| Number of pages | 5 |
| Journal | European Journal of Medicinal Chemistry |
| Volume | 37 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - Jun 2002 |
Keywords
- Acridindione
- Potassium channel openers
- Synthesis
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