Data di Pubblicazione:
2006
Abstract:
Abstract
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 (EC(50)=0.43microM) the affinities for alpha(1A), alpha(1B) and alpha(1D) adrenergic sub-receptors were determined.
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 (EC(50)=0.43microM) the affinities for alpha(1A), alpha(1B) and alpha(1D) adrenergic sub-receptors were determined.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
alpha receptors; phtalazinone; vasorelaxant activity; rat; vas deferens; aorta
Elenco autori:
DEL OLMO, E.; Barboza, B.; Ybarra, M. I.; LOPEZ PREZ, J. L.; Carrn, R.; Sevilla, M. A.; Boselli, Cinzia; SAN FELICIANO, A.
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