4.0 Article

Tecadenoson -: Antiarrhythmic adenosine A1 agonist

期刊

DRUGS OF THE FUTURE
卷 27, 期 9, 页码 846-849

出版社

PROUS SCIENCE, SAU-THOMSON REUTERS
DOI: 10.1358/dof.2002.027.09.695422

关键词

N-6-[3(R)-tetrahydrofuranyl]adenosine

向作者/读者索取更多资源

Adenosine has been shown to be a clinically effective antiarrhythmic agent. However, because it acts on all 4 adenosine cell surface receptors (AdoRs), in addition to the cardiovascular effects beneficial for treating arrhythmias (i ' e., A, egative chronotropic, negative dromotropic, negative inotropic, anti-beta-adrenergic effects) occurring via activation of the A(1) AdoR, adenosine also exerts positive coronary vasodilatory effects via A(2A) AdoR. Thus, clinical use of the agent is associated with unwanted side effects including hypotension. Selective activation of At AdoR would eliminate induction of h tension from the possible cardioprotectant effects adenosine and/or adenosine agonists. Tecadenoson is an agent that has been shown to be highly selective for A(1) AdoR over A(2A) AdoR. It was-selected for further development in controlling heart rate during acute atrial arrhythmias, including conditions of atrial fibrillation, atrial flutter and paroxysmal supraventricular tachycardias (PSVT), without lowering blood pressure.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.0
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据