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 |
卷 | 61 |
發行號 | 1 |
DOIs | |
出版狀態 | Published - 1月 1998 |