The present invention is directed to azetidine compounds that inhibit the glycine transporter GlyT1 and which are useful in the treatment of neurological and psychiatric disorders associated with glycinergic or glutamatergic neurotransmission dysfunction and diseases in which the glycine transporter GlyT1 is involved.
本发明涉及抑制甘
氨酸转运体GlyT1的氮杂四元化合物,这些化合物在治疗与甘
氨酸能或谷
氨酸能神经递质功能障碍有关的神经系统和精神障碍以及涉及甘
氨酸转运体GlyT1的疾病中具有用处。