Litebamine N-homologues: Preparation and anti-acetylcholinesterase activity

Chi Ming Chiou, Jaw Jou Kang, Shoei Sheng Lee*

*此作品的通信作者

研究成果: Article同行評審

42 引文 斯高帕斯(Scopus)

摘要

Litebamine N-homologues were easily prepared from laurolitsine, generally via three reaction steps (N-alkylation, solvolysis with 1 M NH4OAc under reflux, and the Mannich reaction) in more than 80% overall yield. Among the prepared compounds, N-propyl-, N-isobutyl-, and N-isopropylnorlitebamines exhibited moderate antiacetylcholinesterase activity (IC50 ca. 7.0 μM), while the corresponding N-metho salt of N-propylnorlitebamine showed potent activity (IC50 2.70 μM).

原文English
頁(從 - 到)46-50
頁數5
期刊Journal of Natural Products
61
發行號1
DOIs
出版狀態Published - 1月 1998

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