首页> 美国卫生研究院文献>ACS Medicinal Chemistry Letters >Discovery of GSK2193874: An Orally Active Potentand Selective Blocker of Transient Receptor Potential Vanilloid 4
【2h】

Discovery of GSK2193874: An Orally Active Potentand Selective Blocker of Transient Receptor Potential Vanilloid 4

机译:发现GSK2193874:口服活性有力受体潜在性香草醛的选择性阻滞剂4

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Transient Receptor Potential Vanilloid 4 (TRPV4) is a member of the Transient Receptor Potential (TRP) superfamily of cation channels. TRPV4 is expressed in the vascular endothelium in the lung and regulates the integrity of the alveolar septal barrier. Increased pulmonary vascular pressure evokes TRPV4-dependent pulmonary edema, and therefore, inhibition of TRPV4 represents a novel approach for the treatment of pulmonary edema associated with conditions such as congestive heart failure. Herein we report the discovery of an orally active, potent, and selective TRPV4 blocker, 3-(1,4′-bipiperidin-1′-ylmethyl)-7-bromo-N-(1-phenylcyclopropyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxamide (GSK2193874, >28) after addressing an unexpected off-target cardiovascular liability observed from in vivo studies. GSK2193874 is a selective tool for elucidating TRPV4 biology both in vitro and in vivo.
机译:瞬时受体电势Vanilloid 4(TRPV4)是阳离子通道瞬时电势(TRP)超家族的成员。 TRPV4在肺部的血管内皮中表达,并调节肺泡间隔屏障的完整性。升高的肺血管压力会引起TRPV4依赖性肺水肿,因此,抑制TRPV4代表了一种治疗与充血性心力衰竭等疾病相关的肺水肿的新方法。在这里,我们报告发现了口服活性,有效和选择性TRPV4阻滞剂3-(1,4'-bipiperidin-1'-ylmethyl)-7-bromo-N-(1-苯基环丙基)-2- [3- (三氟甲基)苯基] -4-喹啉甲酰胺(GSK2193874,> 28 )解决了体内研究中发现的意外脱靶心血管不良反应。 GSK2193874是用于在体内和体外阐明TRPV4生物学的选择性工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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