The problem of the present invention is to provide a compound having a GR selective binding activity, which shows less action on other nuclear receptors such as progesterone receptor (PR), mineralocorticoid receptor (MR) and the like. The present invention provides a condensed tetrahydroquinoline compound represented by the following formula (I)
wherein each symbol is as defined in the present specification, or a pharmaceutically acceptable salt thereof or a hydrate thereof.
本发明的问题是提供一种具有GR选择性结合活性的化合物,该化合物对于其他核受体,如孕激素受体(PR)、
醛固酮受体(MR)等的作用较少。本发明提供了一种由以下公式(I)表示的紧凑型
四氢喹啉化合物,其中每个符号如本说明书所定义,或其药学上可接受的盐或
水合物。