H. Lundbeck A/S, Department of Medicinal Chemistry, DK-2500 Valby, Denmark.
Bioorg Med Chem. 2013 Oct 1;21(19):6053-62. doi: 10.1016/j.bmc.2013.07.030. Epub 2013 Jul 23.
PDE10A is a recently identified phosphodiesterase with a quite remarkable localization since the protein is abundant only in brain tissue. Based on this unique localization, research has focused extensively on using PDE10A modulators as a novel therapeutic approach for dysfunction in the basal ganglia circuit including Parkinson's disease, Huntington's disease, schizophrenia, addiction and obsessive compulsive disorder. Medicinal chemistry efforts identified the N-methyl-N-[4-(quinolin-2-ylmethoxy)-phenyl]-isonicotinamide (8) as a nanomolar PDE10A inhibitor. A subsequent Lead-optimization program identified analogous N-methylanilides and their corresponding N-methylbenzamides (29) as potent PDE10A inhibitors, concurrently some interesting and unexpected binding modes were identified.
PDE10A 是一种最近被发现的磷酸二酯酶,其具有非常显著的定位,因为该蛋白仅在脑组织中大量存在。基于这种独特的定位,研究广泛集中在使用 PDE10A 调节剂作为一种新的治疗方法,用于治疗基底神经节回路的功能障碍,包括帕金森病、亨廷顿病、精神分裂症、成瘾和强迫症。药物化学研究确定 N-甲基-N-[4-(喹啉-2-基甲氧基)-苯基]-异烟酰胺(8)为纳摩尔 PDE10A 抑制剂。随后的先导优化计划确定了类似的 N-甲基苯胺和相应的 N-甲基苯甲酰胺(29)作为有效的 PDE10A 抑制剂,同时也确定了一些有趣和意外的结合模式。