| Literature DB >> 15120319 |
Giuliana Biagi1, Vincenzo Calderone, Irene Giorgi, Oreste Livi, Enrica Martinotti, Alma Martelli, Antonio Nardi.
Abstract
As part of our program toward designing potassium channel openers, synthesis of a novel series of 1,5-diphenylsubstituted 1,2,3-triazoles, as potential activators of the large-conductance calcium-activated potassium channels (BK), as well as their vasorelaxant activity are presented. The functional effect of these potential structurally novel BK-openers on vascular contractile function were studied in vitro, using isolated rat aortic rings pre-contracted with KCl 20 mM. Among the target compounds, only 16 showed appreciable effectiveness, exhibiting an efficacy parameter (57%) lower than that of NS1619 and a comparable potency index (pIC50: 5.58). Copyright 2004 Elsevier SASEntities:
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Year: 2004 PMID: 15120319 DOI: 10.1016/j.farmac.2004.01.012
Source DB: PubMed Journal: Farmaco ISSN: 0014-827X