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首页> 外文期刊>Journal of Medicinal Chemistry >Selective Kv1.5 Blockers: Development of (R)-1-(Methylsulfonylamino)-3-[2-(4-methoxyphenyl)ethyl]-4-(4-methoxyphe nyl)-2-imidazolidinone (KVI-020/WYE-160020) as a Potential Treatment for Atrial Arrhythmia
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Selective Kv1.5 Blockers: Development of (R)-1-(Methylsulfonylamino)-3-[2-(4-methoxyphenyl)ethyl]-4-(4-methoxyphe nyl)-2-imidazolidinone (KVI-020/WYE-160020) as a Potential Treatment for Atrial Arrhythmia

机译:选择性Kv1.5阻滞剂:(R)-1-(甲基磺酰基氨基)-3- [2-(4-甲氧基苯基)乙基] -4-(4-甲氧基苯甲基)-2-咪唑啉酮(KVI-020 / WYE- 160020)作为房性心律不齐的潜在治疗方法

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摘要

Atrial fibrillation is the most prevalent form of cardiac arrhythmia. Current treatments extend the atrial effective refractory period by nonselective blockade of cardiac ion channels. Ani alternative approach selectively targeting the Kv1.5 ion channel offers the opportunity for therapeutic benefit with decreased risk of adverse cardiovascular events. KVI-020 (4g) successfully demonstrated antiarrhythmic efficacy in a canine arrhythmia model, and these findings support its utility as an antiarrhythmic agent.
机译:心房颤动是心律不齐的最普遍形式。当前的治疗是通过非选择性阻断心脏离子通道来延长心房有效不应期。选择性靶向Kv1.5离子通道的另一种方法为治疗带来了好处,同时降低了不良心血管事件的风险。 KVI-020(4g)在犬心律不齐模型中成功证明了抗心律不齐的功效,这些发现支持了其作为抗心律不齐药物的用途。

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