F. Hoffmann-La Roche Ltd., Pharmaceutical Division, CH-4070 Basel, Switzerland.
J Med Chem. 2010 Jun 24;53(12):4603-14. doi: 10.1021/jm100210p.
The GlyT1 transporter has emerged as a key novel target for the treatment of schizophrenia. Herein, we report on the optimization of the 2-alkoxy-5-methylsulfonebenzoylpiperazine class of GlyT1 inhibitors to improve hERG channel selectivity and brain penetration. This effort culminated in the discovery of compound 10a (RG1678), the first potent and selective GlyT1 inhibitor to have a beneficial effect in schizophrenic patients in a phase II clinical trial.
甘氨酸转运体 1(GlyT1)已成为治疗精神分裂症的一个新的重要靶点。本文报道了对 2-烷氧基-5-甲磺酰基苯甲酰基哌嗪类 GlyT1 抑制剂进行优化,以提高 hERG 通道选择性和脑穿透性。这项工作的最终成果是发现了化合物 10a(RG1678),这是第一个在精神分裂症患者的 II 期临床试验中具有良好疗效的有效且选择性的 GlyT1 抑制剂。