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单胺氧化酶抑制剂的设计。

Inhibitor design for monoamine oxidases.

机构信息

Biomedical Sciences Research Complex, University of St Andrews, Biomolecular Sciences Building, North Haugh, St Andrews, KY16 9ST, UK.

出版信息

Curr Pharm Des. 2013;19(14):2529-39. doi: 10.2174/1381612811319140004.

Abstract

Flavin-containing monoamine oxidases (MAO A and MAO B) located on the outer membrane of mitochondria oxidise amines and generate hydrogen peroxide. Inhibitors alleviate depression by increasing neurotransmitter levels in the brain. Elevation of neurotransmitters,although an established outcome, is a delicate balance because complete lack of MAO A is associated with aggression and combination of monoamine oxidase inhibitors with reuptake inhibitors can result in serotonin toxicity. MAO in the periphery is essential for protection against biogenic amines, so inhibition there is an undesirable side effect both of antidepressants and drugs for other targets.MAO also metabolizes many amine drugs, an important factor in pharmacokinetics. This review summarises the structure, assay and regulation of MAO. The importance of reliable inhibition data properly analysed for these flavoenzymes is emphasised. It describes some current drugs and how new compounds that inhibit MAO are emerging from structure-based drug design.

摘要

黄素单胺氧化酶(MAO A 和 MAO B)位于线粒体的外膜上,可氧化胺类物质并产生过氧化氢。抑制剂通过增加大脑中的神经递质水平来缓解抑郁。神经递质的升高虽然是一种既定的结果,但这是一种微妙的平衡,因为 MAO A 的完全缺乏与攻击性有关,而单胺氧化酶抑制剂与再摄取抑制剂的组合可能导致血清素毒性。外周的 MAO 对于保护生物胺至关重要,因此抑制外周 MAO 既是抗抑郁药的不良副作用,也是其他靶标药物的不良副作用。MAO 还代谢许多胺类药物,这是药代动力学中的一个重要因素。本文综述了 MAO 的结构、测定和调节。强调了为这些黄素酶提供可靠的抑制数据的重要性。它描述了一些当前的药物以及如何通过基于结构的药物设计出现新的抑制 MAO 的化合物。

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