最近的发现表明,人类Na V 1.7通道的突变与疼痛感改变之间的关系有助于增加该离子通道作为潜在镇痛药开发目标的吸引力。酰氨基苯并二氢吡喃1和2被确定为Na V 1.7通道的阻滞剂,并制备了具有5个取代基和羧酰胺部分修饰的类似物,以建立结构与活性的关系。鉴定出具有良好的体外和体内大鼠PK概况的化合物13和29。此外,有29种药物在伤害性疼痛模型中显示出体内功效。
NOVEL N-(8-HETEROARYLTETRAHYDRONAPHTALENE-2YL) OR N-(5-HETEROARYLCHROMANE-3-YL) CARBOXAMIDE DERIVATIVES FOR THE TREATMENT OF PAIN
申请人:Besidski Yevgeni
公开号:US20100137322A1
公开(公告)日:2010-06-03
The present invention relates to new compounds of formula (I) and to pharmaceutical composition containing said compounds and to the use of said compounds in therapy. The present invention further relates to processes for the preparation of said compounds and to new intermediates useful in the preparation thereof.
The present invention relates to new compounds of formula (I) and to pharmaceutical composition containing said compounds and to the use of said compounds in therapy. The present invention further relates to processes for the preparation of said compounds and to new intermediates useful in the preparation thereof.