摘要
Chemical investigation of the red alga Laurencia tristicha led to the discovery of eight new halogenated chamigrane-type sesquiterpenoids (1-8) and one new bromocuparane-type sesquiterpene (9), along with nine known related metabolites (10-18). Their structures were elucidated on the basis of extensive spectroscopic analyses, and the absolute configurations of 1-8 were proposed by comparison to the biosynthetically related known compound 12. Cytotoxicity, antibacterial, and anti-inflammatory activities of these isolates were also investigated. The results showed that compound 11 exhibited good antibacterial activity against Serratia marcescens compared to the positive control ampicillin at a dosage of 100 μg/disk. Compound 17 showed strong inhibition toward elastase release generation at 10 μM.
原文 | 英語 |
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頁(從 - 到) | 2315-2323 |
頁數 | 9 |
期刊 | Journal of Natural Products |
卷 | 79 |
發行號 | 9 |
DOIs | |
出版狀態 | 已出版 - 23 09 2016 |
文獻附註
Publisher Copyright:© 2016 The American Chemical Society and American Society of Pharmacognosy.