Synthesis and Biological Evaluation of Five‐Atom‐Linker‐Based Arylpiperazine Derivatives with an Atypical Antipsychotic Profile
作者:Chunhui Wu、Yu Wang、Feipu Yang、Wenqiang Shi、Zhen Wang、Ling He、Yang He、Jingshan Shen
DOI:10.1002/cmdc.201900439
日期:2019.12.17
Herein we describe a focused set of new arylpiperazine derivatives as potential broad-spectrum antipsychotics. The general structure contains a quinolinone-like moiety, an arylpiperazine moiety, and a five-atom linker. Among them, 7-(5-(4-(benzo[d]isothiazol-4-yl)piperazin-1-yl)pentyl)quinolin-2(1H)-one (S6) shows a promising preclinical profile. Compound S6, characterized by partial D2 R agonism,
在这里,我们描述了一组潜在的广谱抗精神病药新的芳基哌嗪衍生物。总体结构包含喹啉酮样部分,芳基哌嗪部分和五原子接头。其中,7-(5-(4-(苯并[d]异噻唑-4-基)哌嗪-1-基)戊基)喹啉-2(1H)-1(S6)显示出良好的临床前概况。发现化合物S6具有部分D2 R激动作用,5-HT1A R激动作用,5-HT2A R拮抗作用和对SERT活性的阻断作用,可减轻啮齿动物的精神病和抑郁样症状。S6的多药理学特征可为治疗其他各种中枢神经系统疾病(如焦虑症,抑郁症和痴呆症相关的精神病)提供机会。此外,S6表现出可接受的安全性,毒理学和药代动力学特征,