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具有显著情绪调节活性和良好安全性的多功能芳基砜和芳基磺酰胺类配体,靶向痴呆症的神经精神症状。

Multifunctional Arylsulfone and Arylsulfonamide-Based Ligands with Prominent Mood-Modulating Activity and Benign Safety Profile, Targeting Neuropsychiatric Symptoms of Dementia.

作者信息

Marcinkowska Monika, Bucki Adam, Sniecikowska Joanna, Zagórska Agnieszka, Fajkis-Zajączkowska Nikola, Siwek Agata, Gluch-Lutwin Monika, Żmudzki Paweł, Jastrzebska-Wiesek Magdalena, Partyka Anna, Wesołowska Anna, Abram Michał, Przejczowska-Pomierny Katarzyna, Cios Agnieszka, Wyska Elżbieta, Mika Kamil, Kotańska Magdalena, Mierzejewski Paweł, Kolaczkowski Marcin

机构信息

Faculty of Pharmacy, Jagiellonian University Medical College, 9 Medyczna St., 30-688 Krakow, Poland.

Institute of Psychiatry and Neurology, 9 Sobieskiego Street, 02-957 Warsaw, Poland.

出版信息

J Med Chem. 2021 Sep 9;64(17):12603-12629. doi: 10.1021/acs.jmedchem.1c00497. Epub 2021 Aug 26.

DOI:10.1021/acs.jmedchem.1c00497
PMID:34436892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8436213/
Abstract

The current pharmaceutical market lacks therapeutic agents designed to modulate behavioral disturbances associated with dementia. To address this unmet medical need, we designed multifunctional ligands characterized by a nanomolar affinity for clinically relevant targets that are associated with the disease pathology, namely, the 5-HT and D receptors. Compounds that exhibited favorable functional efficacy, water solubility, and metabolic stability were selected for more detailed study. Pharmacological profiling revealed that compound exerted pronounced antidepressant activity (MED 0.1 mg/kg), outperforming commonly available antidepressant drugs, while compound elicited a robust anxiolytic activity (MED 1 mg/kg), exceeding comparator anxiolytics. In contrast to the existing psychotropic agents tested, the novel chemotypes did not negatively impact cognition. At a chronic dose regimen (25 days), did not induce significant metabolic or adverse blood pressure disturbances. These promising therapeutic-like activities and benign safety profiles make the novel chemotypes potential treatment options for dementia patients.

摘要

目前的制药市场缺乏旨在调节与痴呆症相关的行为障碍的治疗药物。为满足这一未得到满足的医疗需求,我们设计了多功能配体,其对与疾病病理相关的临床相关靶点(即5-羟色胺和D受体)具有纳摩尔亲和力。选择表现出良好功能疗效、水溶性和代谢稳定性的化合物进行更详细的研究。药理学分析表明,化合物具有显著的抗抑郁活性(半数有效量为0.1毫克/千克),优于常用的抗抑郁药物,而化合物具有强大的抗焦虑活性(半数有效量为1毫克/千克),超过对照抗焦虑药。与所测试的现有精神药物不同,新型化学类型对认知没有负面影响。在慢性给药方案(25天)下,不会引起明显的代谢或不良血压紊乱。这些有前景的类治疗活性和良好的安全性使新型化学类型成为痴呆症患者潜在的治疗选择。

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