The invention relates to a method for modulating Ca
2+
-release-activated Ca
2+
channels (CRAC) in a cell by administering to the cell a compound of formula (I):
or a pharmaceutically acceptable salt, solvate, clathrate, or prodrug thereof wherein X, Y, A, Z, L and n are defined herein.
本发明涉及一种通过向细胞中给予以下公式(I)的化合物或其药学可接受的盐、溶剂合物、包合物或前药来调节细胞中的Ca2+释放激活的Ca2+通道(C
RAC)的方法,其中X、Y、A、Z、L和n在此定义。