Department of Drug Chemistry and Technologies, Sapienza University of Rome, Rome, Italy.
Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, Chieti, Italy.
Expert Opin Ther Pat. 2022 Aug;32(8):849-883. doi: 10.1080/13543776.2022.2083501. Epub 2022 Jun 9.
Monoamine oxidase (MAO) inhibitors are currently used as antidepressants (selective MAO-A inhibitors) or as co-adjuvants for neurodegenerative diseases (selective MAO-B inhibitors). The research within this field is attracting attention due to their crucial role in the modulation of brain functions, mood, and cognitive activity, and monoamine catabolism.
MAO inhibitors (2018-2021) are discussed according to their chemotypes. Structure-activity relationships are derived for each chemical scaffold (propargylamines, chalcones, indoles, benzimidazoles, (iso)coumarins, (iso)benzofurans, xanthones, and tetralones), while the chemical entities were divided into newly synthesized molecules and natural metabolites. The mechanism of action and type of inhibition are also considered. Lastly, new therapeutic applications are reported, which demonstrates the clinical potential of these inhibitors as well as the possibility of repurposing existing drugs for a variety of diseases.
MAO inhibitors here reported exhibit different potencies and isoform selectivity. These compounds are clinically licensed for multi-faceted neurodegenerative pathologies due to their ability to also act against other relevant targets (cholinesterases, inflammation, and oxidative stress). Moreover, the drug repurposing approach is an attractive strategy by which MAO inhibitors may be applied for the treatment of prostate cancer, inflammation, vertigo, and type 1 diabetes.
单胺氧化酶(MAO)抑制剂目前被用作抗抑郁药(选择性 MAO-A 抑制剂)或神经退行性疾病的辅助药物(选择性 MAO-B 抑制剂)。由于它们在调节大脑功能、情绪和认知活动以及单胺分解代谢方面的关键作用,该领域的研究引起了人们的关注。
根据化学类型讨论了 MAO 抑制剂(2018-2021 年)。为每个化学支架(炔丙胺、查耳酮、吲哚、苯并咪唑、(异)香豆素、(异)苯并呋喃、姜黄素和四氢萘酮)推导了结构-活性关系,同时将化学实体分为新合成的分子和天然代谢物。还考虑了作用机制和抑制类型。最后,报告了新的治疗应用,这表明这些抑制剂具有临床潜力,以及将现有药物重新用于多种疾病的可能性。
本文报道的 MAO 抑制剂表现出不同的效力和同工酶选择性。这些化合物因能够针对其他相关靶点(胆碱酯酶、炎症和氧化应激)而具有多方面的神经退行性病变的临床许可。此外,药物再利用方法是一种有吸引力的策略,通过该策略,MAO 抑制剂可用于治疗前列腺癌、炎症、眩晕和 1 型糖尿病。