...
首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Second generation N-(1,2-diphenylethyl)piperazines as dual serotonin and noradrenaline reuptake inhibitors: improving metabolic stability and reducing ion channel activity.
【24h】

Second generation N-(1,2-diphenylethyl)piperazines as dual serotonin and noradrenaline reuptake inhibitors: improving metabolic stability and reducing ion channel activity.

机译:第二代N-(1,2-二苯乙基)哌嗪作为5-羟色胺和去甲肾上腺素的重摄取抑制剂:改善代谢稳定性并降低离子通道活性。

获取原文
获取原文并翻译 | 示例
           

摘要

New N-(1,2-diphenylethyl)piperazines 6 are disclosed as dual serotonin and noradrenaline reuptake inhibitors (SNRI) which may have potential in treating stress urinary incontinence (SUI). In this Letter, we present new data for SNRI PF-526014 (4) including performance in a canine in vivo model of SUI, cardiovascular assessment, pharmacokinetics in dog and determination of the primary routes of metabolism in vitro. Starting from 4, detailed structure activity relationships established that potent dual SNRIs could be achieved by appropriate substitution of the phenyl rings (6: R; R(1)) combined with a preferred stereochemistry. From this set of compounds, piperazine (-)-6a was identified as a potent and selective dual SNRI with improved metabolic stability and reduced ion channel activity when compared to 4. Based on this profile, (-)-6a was selected for further evaluation in a preclinical model of SUI.
机译:公开了新的N-(1,2-二苯乙基)哌嗪6作为5-羟色胺和去甲肾上腺素再摄取抑制剂(SNRI)的双重用途,它们可能具有治疗压力性尿失禁的潜力。在这封信中,我们介绍了SNRI PF-526014(4)的新数据,包括在SUI犬体内模型中的性能,心血管评估,狗的药代动力学以及体外代谢的主要途径的确定。从4开始,详细的结构活性关系建立了有效的双重SNRIs,可以通过结合苯环(6:R; R(1))与优选的立体化学方法进行适当取代来实现。从这组化合物中,哌嗪(-)-6a被鉴定为有效的和选择性的双重SNRI,与4相比具有改善的代谢稳定性和降低的离子通道活性。基于此特征,选择(-)-6a进行进一步评估在SUI的临床前模型中

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号