Abstract
A recent uroselective α1-adrenoceptor antagonist, REC15/2739, has been joined with nitrooxy and furoxan NO-donor moieties to give new NO-donor α1-antagonists. All the compounds studied proved to be potent and selective ligands of human cloned α 1a-receptor subtype. Derivatives 6 and 7 were able to relax the prostatic portion of rat vas deferens contracted by (-)-noradrenaline because of both their α1A-antagonist and their NO-donor properties.
Lingua originale | Inglese |
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pagine (da-a) | 3762-3765 |
Numero di pagine | 4 |
Rivista | Journal of Medicinal Chemistry |
Volume | 46 |
Numero di pubblicazione | 17 |
DOI | |
Stato di pubblicazione | Pubblicato - 14 ago 2003 |