| Literature DB >> 27536968 |
Jia-Yu Chen, Chiung-Yao Huang, Yun-Sheng Lin1, Tsong-Long Hwang2, Wei-Lung Wang3, Shu-Fen Chiou, Jyh-Horng Sheu4,5.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27536968 DOI: 10.1021/acs.jnatprod.6b00452
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050