Design and Optimization of Sulfone Pyrrolidine Sulfonamide Antagonists of Transient Receptor Potential Vanilloid-4 with in Vivo Activity in a Pulmonary Edema Model
作者:Joseph E. Pero、Jay M. Matthews、David J. Behm、Edward J. Brnardic、Carl Brooks、Brian W. Budzik、Melissa H. Costell、Carla A. Donatelli、Stephen H. Eisennagel、Karl Erhard、Michael C. Fischer、Dennis A. Holt、Larry J. Jolivette、Huijie Li、Peng Li、John J. McAtee、Brent W. McCleland、Israil Pendrak、Lorraine M. Posobiec、Katrina L.K. Rivera、Ralph A. Rivero、Theresa J. Roethke、Matthew R. Sender、Arthur Shu、Lamont R. Terrell、Kalindi Vaidya、Xiaoping Xu、Brian G. Lawhorn
DOI:10.1021/acs.jmedchem.8b01344
日期:2018.12.27
ailment of heart failure patients and has remained an unmet medical need due to dose-limiting side effects associated with current treatments. Preclinical studies in rodents have suggested that inhibition of transient receptor potential vanilloid-4 (TRPV4) cation channels may offer an alternative—and potentially superior—therapy. Efforts directed toward small-molecule antagonists of the TRPV4 receptor
肺水肿是心力衰竭患者的常见疾病,由于与当前治疗方法相关的剂量限制副作用,其仍未满足医疗需求。啮齿动物的临床前研究表明,抑制瞬时受体电位香草酸4(TRPV4)阳离子通道可能提供替代方法,并且可能具有更好的治疗效果。针对TRPV4受体的小分子拮抗剂的努力已经导致发现了新型的以吡咯烷6为代表的砜吡咯烷磺酰胺化学型。描述了优化TRPV4活性,选择性和药代动力学特性的设计要素。领先榜样19和27的活动 在本文中强调了体内模型中暗示治疗潜力的模型。