10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Cytotoxic dolabellane diterpenes from the Formosan soft coral Clavularia inflata.

      Journal of Natural Products
      Animals, Antineoplastic Agents, chemistry, isolation & purification, pharmacology, Carcinoma, Squamous Cell, Cnidaria, Diterpenes, Humans, Leukemia P388, Lung Neoplasms, Magnetic Resonance Spectroscopy, Mass Spectrometry, Mice, Molecular Structure, Spectrophotometry, Infrared, Spectrophotometry, Ultraviolet, Stereoisomerism, Taiwan, Tumor Cells, Cultured, drug effects

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Six new cytotoxic dolabellane diterpenes, (1R,12R)-dolabella-4(16),7,10-triene-3,13-dione (1), (1R*,7R*,8S*,12R*)-dolabella-4(16),10-diene-7,8-epoxy- 3,13-dione (2), (1R*,10R*,11S*,12R*)-dolabella-4(16),7-diene-10,11-epoxy-3,13-dione (3), (1R)-dolabella-4(16),7,11(12)-triene-3,13-dione (4), (1R*,3R*)-3-hydroxydolabella-4(16),7,11(12)-triene-3,13-dione (5), and (1R*,7R*)-7-hydroperoxydolabella-4(16),8(17),11(12)-triene-3,13-dione (6), have been isolated from the Formosan soft coral Clavularia inflata. The structures of compounds 1-6 were determined by 1D and 2D spectral analysis, and their cytotoxicity against selected cancer cells was measured in vitro.

          Related collections

          Author and article information

          Comments

          Comment on this article