Chao, Chih-HuaChih-HuaChaoHuang, Ho-ChengHo-ChengHuangWu, Yang-ChangYang-ChangWuLu, Chung-KuangChung-KuangLuCHANG-FENG DAISheu, Jyh-HorngJyh-HorngSheu2009-12-172018-06-282009-12-172018-06-282007http://www.scopus.com/inward/record.url?eid=2-s2.0-36849003859&partnerID=MN8TOARShttp://scholars.lib.ntu.edu.tw/handle/123456789/330546http://ntur.lib.ntu.edu.tw/bitstream/246246/174454/1/70.pdfThree glycolipids (1-3), possessing a sugar moiety at C-2 of glycerol ether, have been isolated from the Formosan soft coral Lobophytum crassum. Their structures were elucidated by spectroscopic methods, particularly in 1D- and 2D-NMR experiments. The absolute configurations on the sugar portion and lipid aglycon of 1-3 were determined by methanolysis, chemical transformation and the application of Mosher's method on 1 and 3. Compounds 1-3 exhibited weak cytotoxic activities. ? 2007 Pharmaceutical Society of Japan.application/pdf133384 bytesapplication/pdfen-USArabinopyranoside; Coral; Glycolipid; Lobophytum crassum; R-batyl alcohol; R-chimyl alcohol[SDGs]SDG3[SDGs]SDG141 acetoxy 3 hexadecyloxypropyl beta dextro arabinopyranoside; 1 hydroxy 3 hexadecyloxypropyl beta dextro arabinopyranoside; 1 hydroxy 3 octadecyloxypropyl beta dextro arabinopyranoside; glycolipid; unclassified drug; article; cancer cell; controlled study; coral; cytotoxicity; drug isolation; drug structure; drug transformation; human; human cell; Lobophytum crassum; methanolysis; nuclear magnetic resonance spectroscopy; proton nuclear magnetic resonance; Animals; Anthozoa; Antineoplastic Agents; Cell Line, Tumor; Chromatography, Thin Layer; Drug Screening Assays, Antitumor; Glycolipids; Humans; Hydrolysis; Indicators and Reagents; Mass Spectrometry; Taiwanjournal article10.1248/cpb.55.17202-s2.0-36849003859WOS:000258681600011http://ntur.lib.ntu.edu.tw/bitstream/246246/174454/1/70.pdf