首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Design, synthesis and biological evaluation of novel chiral oxazino-indoles as potential and selective neuroprotective agents against A beta(25-35)-induced neuronal damage
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Design, synthesis and biological evaluation of novel chiral oxazino-indoles as potential and selective neuroprotective agents against A beta(25-35)-induced neuronal damage

机译:设计,合成和生物学评价新型手性恶嗪吲哚作为潜在和选择性的神经保护剂,针对A beta(25-35)诱导的神经元损伤。

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摘要

A series of chiral oxazino-indoles have been synthesized via a key intermolecular oxa-Pictet-Spengler reaction. These compounds exhibited significant and selective neuroprotective effects against A beta(25-35)-induced neuronal damage. This is the first report of evaluating the influence of chiral diversity of oxazino-indoles on their neuroprotective activities, with the structure-activity relationship been analyzed. The highly active compounds 3f, 3g, 4g, 4h, and 6b all performed over 90% cell protection, providing a new direction for the development of neuroprotective agents against Alzheimer's disease. (C) 2016 Elsevier Ltd. All rights reserved.
机译:通过关键的分子间氧杂-Pictet-Spengler反应合成了一系列手性恶嗪-吲哚。这些化合物显示出针对A beta(25-35)诱导的神经元损害的重大和选择性的神经保护作用。这是评价恶嗪-吲哚的手性多样性对其神经保护活性影响的第一份报告,并分析了其结构-活性关系。高活性化合物3f,3g,4g,4h和6b均具有超过90%的细胞保护作用,为开发抗阿尔茨海默氏病的神经保护剂提供了新的方向。 (C)2016 Elsevier Ltd.保留所有权利。

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