Molecular Neuropharmacology Section, NINDS, National Institutes of Health, Bethesda, MD, United States.
Specialized Chemistry Center, University of Kansas, Lawrence, KS, United States.
Bioorg Med Chem Lett. 2021 Jan 1;31:127696. doi: 10.1016/j.bmcl.2020.127696. Epub 2020 Nov 19.
MLS1082 is a structurally novel pyrimidone-based D1-like dopamine receptor positive allosteric modulator. Potentiation of D1 dopamine receptor (D1R) signaling is a therapeutic strategy for treating neurocognitive disorders. Here, we investigate the relationship between D1R potentiation and two prominent structural features of MLS1082, namely the pendant N-aryl and C-alkyl groups on the pyrimidone ring. To this end, we synthesized 24 new analogues and characterized their ability to potentiate dopamine signaling at the D1R and the closely related D5R. We identified structure-activity relationship trends for both aryl and alkyl modifications and our efforts afforded several analogues with improvements in activity. The most effective analogues demonstrated an approximately 8-fold amplification of dopamine-mediated D1R signaling. These findings advance the understanding of structural moieties underlying the activity of pyrimidone-based D1R positive allosteric modulators.
MLS1082 是一种结构新颖的嘧啶酮类 D1 样多巴胺受体正变构调节剂。增强 D1 多巴胺受体 (D1R) 信号转导是治疗神经认知障碍的一种治疗策略。在这里,我们研究了 D1R 增强作用与 MLS1082 两个突出结构特征之间的关系,即嘧啶酮环上的悬垂 N-芳基和 C-烷基。为此,我们合成了 24 种新的类似物,并研究了它们在 D1R 和密切相关的 D5R 上增强多巴胺信号的能力。我们确定了芳基和烷基修饰的构效关系趋势,我们的努力提供了一些具有活性改善的类似物。最有效的类似物表现出多巴胺介导的 D1R 信号的约 8 倍放大。这些发现加深了对基于嘧啶酮的 D1R 正变构调节剂活性的结构部分的理解。