Porter Matthew R, Xiao Haiyan, Maity Sanjay, Vail Nora, Smith Sylvia B, Topczewski Joseph J
Department of Chemistry, University of Minnesota Twin Cities, Minneapolis, Minnesota 55455, United States.
Department of Cellular Biology and Anatomy, Medical College of Georgia at Augusta University, Augusta, Georgia 30912, United States.
ACS Omega. 2020 Dec 11;5(50):32724-32737. doi: 10.1021/acsomega.0c05117. eCollection 2020 Dec 22.
The σ receptor is implicated in regulating a diverse range of physiology and is a target for developing therapies for cancer, pain management, neural degradation, and COVID-19. This report describes 36 phenethylamine-containing 3-amino-chromane ligands, which bind to σ with low nM affinities. The family consists of 18 distinct compounds and each enantiomer was independently assayed. Three compounds with the greatest affinity bind in the 2 nM range (∼8.7 p ). Furthermore, ligands with the (3,4) absolute stereochemistry on the 3-amino-chromane core have a higher affinity and greater σ versus TMEM97 selectivity. The most promising ligands were assayed in 661W cells, which did not show significant protective effects.
σ受体参与调节多种生理功能,是开发癌症、疼痛管理、神经退行性变和COVID-19治疗方法的靶点。本报告描述了36种含苯乙胺的3-氨基色满配体,它们以低纳摩尔亲和力与σ结合。该家族由18种不同的化合物组成,每种对映体都进行了独立检测。三种亲和力最高的化合物在2 nM范围内结合(约8.7 p)。此外,3-氨基色满核心上具有(3,4)绝对立体化学的配体具有更高的亲和力和更大的σ与TMEM97选择性。在661W细胞中对最有前景的配体进行了检测,结果未显示出显著的保护作用。