Synthesis, binding affinity and SAR of new benzolactam derivatives as dopamine D3 receptor ligands
作者:Raquel Ortega、Enrique Raviña、Christian F. Masaguer、Filipe Areias、José Brea、María I. Loza、Laura López、Jana Selent、Manuel Pastor、Ferran Sanz
DOI:10.1016/j.bmcl.2009.01.067
日期:2009.3
series of new benzolactam derivatives was synthesized and the derivatives were evaluated for their affinities at the dopamine D1, D2, and D3 receptors. Some of these compounds showed high D2 and/or D3 affinity and selectivity over the D1 receptor. The SAR study of these compounds revealed structural characteristics that decisively influenced their D2 and D3 affinities. Structural models of the complexes
合成了一系列新的苯并内酰胺衍生物,并评估了它们在多巴胺D 1,D 2和D 3受体上的亲和力。这些化合物中的一些显示出比D 1受体更高的D 2和/或D 3亲和力和选择性。这些化合物的SAR研究揭示了决定性地影响其D 2和D 3亲和力的结构特征。该系列一些最具代表性的化合物与D 2和D 3之间的配合物的结构模型获得受体的目的是使观察到的实验结果合理化。此外,选定的化合物对5-HT 2A表现出中等的结合亲和力,这可能有助于减少作为潜在抗精神病药的锥体束外副作用的发生。