Erythrina Alkaloid Analogues As Nachr Antagonists-A Flexible Platform For Leads In Drug Discovery

JOURNAL OF ORGANIC CHEMISTRY(2021)

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摘要
Erythrina alkaloids and their central nervous system effects have been studied for over a century, mainly due to their potent antagonistic actions at beta 2-containing nicotinic acetylcholine receptors (nAChRs). In the present work, we report a synthetic approach giving access to a diverse set of Erythrina natural product analogues and present the enantioselective total synthesis of (+)-Cocculine and (+)-Cocculidine, both found to be potent antagonists of the beta 2-containing nAChRs.
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