摘要
Abiestetranes A (1) and B (2), two unique tetraterpenes formed by Diels-Alder cycloaddition between a lanostane triterpenoid and a monoterpenoid, were isolated from Abies fabri. Their structures were elucidated by extensive analysis of NMR data. The electronic circular dichroism was utilized to assign the absolute configuration of 1. Compounds 1 and 2 showed significant cytotoxic activities against ZR-75-30 tumor cell with IC 50 values of 6.26 and 1.63 μg/mL, respectively.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 7763-7767 |
| 页数 | 5 |
| 期刊 | Tetrahedron |
| 卷 | 68 |
| 期 | 38 |
| DOI | |
| 出版状态 | 已出版 - 23 9月 2012 |
| 已对外发布 | 是 |
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