Suppr超能文献

新型螺环乙内酰脲衍生物作为一种有效的多受体活性抗精神病和抗抑郁药物。

Novel spirohydantoin derivative as a potent multireceptor-active antipsychotic and antidepressant agent.

作者信息

Czopek Anna, Kołaczkowski Marcin, Bucki Adam, Byrtus Hanna, Pawłowski Maciej, Kazek Grzegorz, Bojarski Andrzej J, Piaskowska Agata, Kalinowska-Tłuścik Justyna, Partyka Anna, Wesołowska Anna

机构信息

Department of Pharmaceutical Chemistry, Jagiellonian University Medical College, 9 Medyczna Street, 30-688 Kraków, Poland.

Department of Pharmaceutical Chemistry, Jagiellonian University Medical College, 9 Medyczna Street, 30-688 Kraków, Poland.

出版信息

Bioorg Med Chem. 2015 Jul 1;23(13):3436-47. doi: 10.1016/j.bmc.2015.04.026. Epub 2015 Apr 16.

Abstract

A series of novel spirohydantoin derivatives with arylpiperazinylbutyl moiety were synthesized and evaluated for serotonin 5-HT1A, 5-HT2A, 5-HT7 and dopamine D2 receptors. Based on these data, four compounds were selected for further binding affinity assays on dopamine D1, D3, D4, and 5-HT2C, 5-HT6 as well as adrenergic α1 and α2C receptors, which are involved in various CNS diseases such as schizophrenia, anxiety and/or depression. The compound 14, 1-{4-[4-(2-metoxyphe-nyl)piperazin-1-yl]butyl}-3',4'-dihydro-2H,2'H,5H-spiro[imidazolidine-4,1'-naphthalene]-2,5-dione, with the most promising functional profile, mixed 5-HT2A/D2 antagonist and 5-HT1A partial agonist, was selected. In the mouse d-amphetamine-induced locomotor hyperactivity model, compound 14 produced antipsychotic-like activity, which is devoid of cataleptogenic effects and in the forced swim test in mice, it showed a significant antidepressant-like effect unlike the reference drug aripiprazole.

摘要

合成了一系列带有芳基哌嗪基丁基部分的新型螺乙内酰脲衍生物,并对其进行了血清素5-HT1A、5-HT2A、5-HT7和多巴胺D2受体的评估。基于这些数据,选择了四种化合物对多巴胺D1、D3、D4以及5-HT2C、5-HT6以及肾上腺素能α1和α2C受体进行进一步的结合亲和力测定,这些受体与精神分裂症、焦虑症和/或抑郁症等各种中枢神经系统疾病有关。化合物14,1-{4-[4-(2-甲氧基苯基)哌嗪-1-基]丁基}-3',4'-二氢-2H,2'H,5H-螺[咪唑烷-4,1'-萘]-2,5-二酮,具有最有前景的功能特征,是5-HT2A/D2混合拮抗剂和5-HT1A部分激动剂,被选中。在小鼠d-苯丙胺诱导的运动性多动模型中,化合物14产生了抗精神病样活性,没有致僵作用,并且在小鼠强迫游泳试验中,与参比药物阿立哌唑不同,它显示出显著的抗抑郁样作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验