The present invention provides substituted pyrrolidines that affect certain excitatory amino acid receptors, and are useful in the treatment of neurological disorders and psychiatric disorders. Specifically, the compounds of the present invention are active as agonists of the metabotropic glutamate receptor subtype mGluR2.
The compounds have the formula
where R¹ and R are independently carboxylic acid or 5-tetrazolyl, or a pharmaceutically acceptable salt or solvate thereof.
本发明提供了影响某些兴奋性
氨基酸受体的取代
吡咯烷类化合物,可用于治疗神经系统疾病和精神疾病。具体来说,本发明的化合物作为代谢型谷
氨酸受体亚型 mGluR2 的激动剂具有活性。
这些化合物具有如下式子
其中 R¹ 和 R 独立地为
羧酸或 5-
四唑基,或其药学上可接受的盐或溶液。