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Multitarget-Directed Ligands Combining Cholinesterase and Monoamine Oxidase Inhibition with Histamine H3R Antagonism for Neurodegenerative Diseases

机译:多靶点配体结合胆碱酯酶和单胺氧化酶抑制与组胺H3R拮抗神经退行性疾病

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摘要

The therapy of complex neurodegenerative diseases requires the development of multitarget-directed drugs (MTDs). Novel indole derivatives with inhibitory activity towards acetyl/butyrylcholinesterases and monoamine oxidases A/B as well as the histamine H receptor (H3R) were obtained by optimization of the neuroprotectant ASS234 by incorporating generally accepted H3R pharmacophore motifs. These small-molecule hits demonstrated balanced activities at the targets, mostly in the nanomolar concentration range. Additional in vitro studies showed antioxidative neuroprotective effects as well as the ability to penetrate the blood–brain barrier. With this promising in vitro profile, contilisant (at 1 mg kg i.p.) also significantly improved lipopolysaccharide-induced cognitive deficits.
机译:复杂的神经退行性疾病的治疗需要开发多靶标定向药物(MTD)。通过掺入普遍认可的H3R药效基团来优化神经保护剂ASS234,可获得对乙酰基/丁酰胆碱酯酶和单胺氧化酶A / B具有抑制活性的新型吲哚衍生物以及组胺H受体(H3R)。这些小分子命中物显示了在靶标上的平衡活性,主要是在纳摩尔浓度范围内。其他体外研究显示抗氧化神经保护作用以及穿透血脑屏障的能力。有了这种有前途的体外特性,助剂(以1 mg kg i.p.)可以显着改善脂多糖诱导的认知功能障碍。

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