Chen, Shin-PinShin-PinChenChao, Chih-HuaChih-HuaChaoHuang, Ho-ChengHo-ChengHuangWu, Yang-ChangYang-ChangWuLu, Chung-KuangChung-KuangLuCHANG-FENG DAISheu, Jyh-HorngJyh-HorngSheu2009-12-172018-06-282009-12-172018-06-282006http://www.scopus.com/inward/record.url?eid=2-s2.0-33750583963&partnerID=MN8TOARShttp://scholars.lib.ntu.edu.tw/handle/123456789/322445http://ntur.lib.ntu.edu.tw/bitstream/246246/174444/1/60.pdfSeven new β-caryophyllene-derived terpenoids (1-7) were isolated from EtOAc extracts of the Formosan soft coral Sinularia gibberosa. The structures of compounds 1-7 were elucidated on the basis of extensive spectroscopic analyses and by comparison with the spectral data of related metabolites. Cytotoxicity evaluation of the above metabolites towards a limited panel of cancer cell lines also will be described. ? 2006 The Chemical Society of Japan.application/pdf113428 bytesapplication/pdfen-US[SDGs]SDG3Cells; Metabolites; Reaction kinetics; Spectroscopic analysis; Tumors; Caryophyllene; Sinularia gibberosa; Soft coral; Aromatic compounds; plant extract; Sinularia gibberosa extract; unclassified drug; article; cancer cell; coral; cytotoxicity; drug isolation; nuclear magnetic resonance; spectroscopyjournal article10.1246/bcsj.79.15472-s2.0-33750583963http://ntur.lib.ntu.edu.tw/bitstream/246246/174444/1/60.pdf