經取代２－（－６－基氧基）－噻唑類及其作為醫藥品之用途农业专利-农业专业知识服务系统

发明人:: CZECHTIZKY, WERNGARD,赛奇兹基　温卡德,賽奇茲基　溫卡德,WESTON, JOHN,韦斯顿　约翰,韋斯頓　約翰,RACKELMANN, NILS,瑞克曼　尼尔,瑞克曼　尼爾,PODESCHWA, MICHAEL,波德舒瓦　麦克,波德舒瓦　麥克,ARNDT, PETRA,阿恩特　佩特拉,WIRTH, KLAUS,维尔特　克劳斯,維爾特　克勞斯,GOEGELEIN,,赛奇兹基温卡德,賽奇茲基溫卡德,韦斯顿约翰,韋斯頓約翰,瑞克曼尼尔,瑞克曼尼爾,波德舒瓦麦克,波德舒瓦麥克,阿恩特佩特拉,维尔特克劳斯,維爾特克勞斯

摘要：: The present invention relates to substituted 2-(chroman-6-yloxy)-thiazoles of the formula I, in which Ar, R2, R3 and R4 are as defined in the claims. the compounds of the formula I are inhibitors of the sodium-calcium exchanger (NCX), especially of the sodium-calcium exchanger of subtype 1 (NCX1), and are suitable for the treatment of diverse disorders in which intracellular calcium homeostasis is disturbed, such as arrhythmias, heart failure and stroke. The invention furthermore relates to processes for the preparation of the compounds of the formula I, their use as pharmaceuticals, and pharmaceutical compositions comprising them.本發明係關於式I之經取代2-(-6-基氧基)-噻唑類，其中Ar、R2、R3及R4具有在申請專利範圍中所指出之意義。式I化合物是鈉-鈣交換體(NCX)之抑制劑，尤其是亞型1之鈉-鈣交換體(NCX1)，且合適用於治療多種疾病其中細胞內鈣恆定平衡受到干擾，例如心律不整、心臟衰竭及中風。本發明還關於式I化合物之製備方法、其作為藥劑之用途及含彼之醫藥組成物。