Design, synthesis and vasorelaxant activity of R, S-1-(substituted phenyl)-4-3-(naphtha-1-yl-oxy)-2-hydroxypropyl-piperazine derivatives.
- Author:
Xiao-zhong FU
1
;
Lei TANG
;
Mu YUAN
;
Jing-shan SHI
Author Information
1. School of Pharmacy, Guiyang Medical College, Guiyang 550004, China.
- Publication Type:Journal Article
- MeSH:
Adrenergic alpha-1 Receptor Antagonists;
Animals;
Antihypertensive Agents;
chemical synthesis;
chemistry;
pharmacology;
In Vitro Techniques;
Molecular Structure;
Piperazines;
chemical synthesis;
chemistry;
pharmacology;
Rabbits;
Structure-Activity Relationship;
Vasoconstriction;
drug effects
- From:
Acta Pharmaceutica Sinica
2007;42(7):735-740
- CountryChina
- Language:Chinese
-
Abstract:
According to the results of activity-structure relationship (SAR) studies of alpha1-adrenoceptor antagonists hydantoin-phenylpiperazine and benzimidazo-arypiperazine derivatves, to design and synthesize a series of novel phenylpiperazine alpha1-adrenoceptor antagonists with more potent vasorelaxant activity, active metabolites of naftopidil were used as lead compounds. Ten novel R,S-1-substituted phenyl-4-[3-(naphthal-yl-oxy)-2-hydroxy propyl]-piperazine were designed and synthesized, their vasorelaxant activity was evaluated by calculating inhibition rate of phenylephrine-induced vasocontration of rabbit artery trips. Five compounds exhibited vasorelaxant activity, and compound 16 showed significant vasorelaxant activity in vitro. At 0.01 and 1 micromol x L(-1), its inhibition rates were 7.03% and 22.72%, respectively. This compound possessed ideal vasorelaxant activity in vitro, and would be selected for further anti-hypertension evaluation in vivo. Moreover, by analyzing the primary activity and structure relationship of these compounds, it could be concluded that the SAR results of the reported phenylpiperazine alpha1-adrenoceptor antagonists could be used for reference in designing novel derivatives of naftopidil with optimal pharmacological properties.
