Chemical constituents of the red alga Laurencia tristicha |
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Authors: | JIE Sun DA-YONG Shi SHUAI Li SU-JUAN Wang LI-JUN Han XIAO Fan |
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Affiliation: | 1. Institute of Oceanology, Chinese Academy of Sciences , Qingdao, 266071, China;2. College of Life Science, Ludong University , Yantai, 264025, China;3. College of Life Science, Ludong University , Yantai, 264025, China;4. Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College (Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education) , Beijing, 100050, China;5. Institute of Oceanology, Chinese Academy of Sciences , Qingdao, 266071, China |
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Abstract: | Six new sesquiterpenes, 10-hydroxy-epiaplysin (1), 10-hydroxy-aplysin (2), 10-hydroxy-debromoepiaplysin (3), aplysin-9-ene (4), epiaplysinol (5) and debromoepiaplysinol (6), together with 13 known compounds (7–19), have been isolated from the red alga Laurencia tristicha. The structures of 1–6 were determined by spectroscopic methods including IR, EI-MS, HREI-MS, and 1D and 2D NMR techniques. All compounds were obtained from this species for the first time and were tested for cytotoxic activities against several human cancer cell lines including lung adenocarcinoma (A549), stomach cancer (BGC-823), hepatoma (Bel 7402), colon cancer (HCT-8) and HeLa cell lines. Compound 6 showed selective cytotoxicity against HeLa cell line with IC50 15.5 μM, cholest-5-en-3β,7α-diol (14) was toxic to all tested cell lines with IC50 values of 16.8, 5.1, 0.5, 0.5, and 0.3 μM, respectively, and other compounds were inactive (IC50>10 μg/ml). |
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Keywords: | Red alga Laurencia tristicha Chemical constituents |
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