| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1378889 | Bioorganic & Medicinal Chemistry Letters | 2006 | 5 Pages |
Several series of dihydrostilbenamide, imidazo[2,1-a]isoindole, pyrimido[2,1-a]isoindole and phthalazinone derivatives were obtained and their vasorelaxant activity was measured on isolated rat aorta rings pre-contracted with phenylephrine (10−5 M). Some phthalazinones attained, practically, the total relaxation of the organ at micromolar concentrations. For the most potent compound 9h (EC50 = 0.43 μM) the affinities for α1A, α1B and α1D adrenergic sub-receptors were determined.
Graphical abstractThe vasorelaxant activity of some dihydrostilbenamides, imidazo[2,1-a]isoindoles, pyrimido[2,1-a]isoindoles and phthalazinones has been evaluated. Three phthalazinones reverted the 10 μM phenylephrine induced contraction with EC50 < 1μM. The affinities of compound 9h for α1A, α1B and α1D adrenergic sub-receptors have been determined.Figure optionsDownload full-size imageDownload as PowerPoint slide
