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设计、合成及新型氯胺酮衍生物作为 NMDA 受体拮抗剂的生物评价。

Design, Synthesis and Biological Evaluation of Novel Ketamine Derivatives as NMDAR Antagonists.

机构信息

Qingyuan Innovation Laboratory, Quanzhou 362801, China.

Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 201203, China.

出版信息

Molecules. 2024 May 23;29(11):2459. doi: 10.3390/molecules29112459.

Abstract

Depression is a chronic, severe, and often life-threatening neurological disorder. It not only causes depression in patients and affects daily life but, in severe cases, may lead to suicidal behavior and have adverse effects on families and society. In recent years, it has been found that sub-anesthetic doses of ketamine have a rapid antidepressant effect on patients with treatment-resistant depression and can significantly reduce the suicidal tendencies of patients with major depressive disorder. Current studies suggest that ketamine may exert antidepressant effects by blocking NMDAR ion channels, but its anesthetic and psychotomimetic side effects limit its application. Here, we report efforts to design and synthesize a novel series of ketamine derivatives of NMDAR antagonists, among which compounds and have improved activity compared with ketamine, introducing a new direction for the development of rapid-acting antidepressant drugs.

摘要

抑郁症是一种慢性、严重且常常危及生命的神经障碍。它不仅会使患者感到沮丧,影响日常生活,在严重的情况下,还可能导致自杀行为,对家庭和社会产生不良影响。近年来,研究发现亚麻醉剂量的氯胺酮对治疗抵抗性抑郁症患者具有快速抗抑郁作用,并能显著降低重度抑郁症患者的自杀倾向。目前的研究表明,氯胺酮可能通过阻断 NMDA 受体离子通道发挥抗抑郁作用,但它的麻醉和致幻副作用限制了它的应用。在这里,我们报告了设计和合成一系列新型 NMDA 受体拮抗剂氯胺酮衍生物的努力,其中化合物 和 与氯胺酮相比活性提高,为开发快速作用抗抑郁药物提供了新的方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2e3/11173549/addf12b7c037/molecules-29-02459-g001.jpg

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