Na V 1.7离子通道是潜在的止痛药开发的一个有吸引力的目标,它基于通道蛋白编码基因的突变与可遗传的疼痛状况之间的牢固遗传联系。的(小号) - ñ -苯并二氢吡喃-3-基羧系列,通过举例说明1,被用作新的通道阻滞剂发展的起始点,导致苯乙烟酰胺系列。建立了该系列的结构和活性之间的关系,并通过适当的替代解决了早期类似物的代谢问题。化合物33显示出可接受的总体体外特性和体内大鼠PK谱。
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.
N-(8-heteroaryltetrahydronaphtalene-2yl) or N-(5-heteroarylchromane-3-yl) carboxamide derivatives for the treatment of pain
申请人:AstraZeneca AB
公开号:US08143408B2
公开(公告)日:2012-03-27
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.