Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1368555 | Bioorganic & Medicinal Chemistry Letters | 2016 | 5 Pages |
Abstract
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 Aβ25–35-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.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jing Chen, Ling-Xue Tao, Wei Xiao, Sha-Sha Ji, Jian-Rong Wang, Xu-Wen Li, Hai-Yan Zhang, Yue-Wei Guo,