| Molecules | |
| Sesquiterpenes from Laurencia similis | |
| Hua Su1  Da-Yong Shi1  Jing Li1  Shu-Ju Guo1  Li-Li Li1  Zhao-Hui Yuan1  | |
| [1] 1Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China 2Graduate School of the Chinese Academy of Sciences, Beijing 100049, China | |
| 关键词: Laurencia similis; sesquiterpenes; cytotoxic assay; | |
| DOI : 10.3390/molecules14051889 | |
| 来源: mdpi | |
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【 摘 要 】
One new sesquiterpene, (4E)-1-bromo-5-[(1'S*,3'R*)-3'-bromo-2',2'-dimethyl-6'-methylenecyclohexyl]-3-methylpent-4-ene-2,3-diol (1), and fifteen known sesquiterpenes, isopalisol (2), luzonensol (3), palisadin B (4), aplysistatin (5), palisadin A (6), 4-hydroxyl-palisudin C (7), 5-acetoxypalisadin B (8), 10-hydroxyaristolan-9-one (9), aristol-8-en-1-one (10), aristolan-9-en-1-one (11), aristolan-1(10)-en-9-one (12), aristolan-1(10)-en-9-ol (13), aristolan-1(10),8-diene (14), aristolan-1,9-diene (15) and aristofone (16), were isolated from a sample of marine red alga Laurencia similis. Their structures were established by detailed NMR spectroscopic analysis and comparison with literature data. Compounds 2-9, and 16 were isolated for the first time from this species. All these metabolites were submitted for a cytotoxicity assay against the tumor cell line BEL7402 (human liver adenocarcinoma), but all of them were found inactive (IC50 > 10 μg/mL).
【 授权许可】
CC BY
This is an open access article distributed under the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202003190056649ZK.pdf | 193KB |
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