Planta Med 2016; 82(09/10): 882-887
DOI: 10.1055/s-0042-106168
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Unusual Cytotoxic Steroidal Saponins from the Gorgonian Astrogorgia dumbea

Autoren

  • Ya-Nan Lu

    1   Key Laboratory of East China Sea & Oceanic Fishery Resources Exploitation and Utilization, Ministry of Agriculture, East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shanghai, P. R. China
  • Ping Cui

    2   Changchun University of Chinese Medicine, Changchun, P. R. China
  • Xiao-Qing Tian

    1   Key Laboratory of East China Sea & Oceanic Fishery Resources Exploitation and Utilization, Ministry of Agriculture, East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shanghai, P. R. China
  • Li-Guang Lou

    3   Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, P. R. China
  • Cheng-Qi Fan

    1   Key Laboratory of East China Sea & Oceanic Fishery Resources Exploitation and Utilization, Ministry of Agriculture, East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shanghai, P. R. China
Weitere Informationen

Publikationsverlauf

received 09. September 2015
revised 11. März 2016

accepted 22. März 2016

Publikationsdatum:
28. Juni 2016 (online)

Abstract

Three steroidal saponins, including astrogorgiosides A (1) and B (2) bearing acetamido-glucose moieties, and astrogorgioside C (3) with a 19-nor and bearing an aromatized B ring steroid aglycone, together with a known major saponin dimorphoside A (4), were obtained from the gorgonian Astrogorgia dumbea collected near Dongshan Island in East China Sea. Structures of these compounds were elucidated by in-depth spectral and chemical methods, including 2D-NMR, HR-ESI-MS spectra, and acidic hydrolysis. For the first time, acetamido-glucose moiety is being reported from a gorgonian. The B-ring aromatized steroid aglycone of compound 3 is also rare in marine natural products. Compounds 13 exhibited moderate cytotoxic activity with IC50 values of 26.8–45.6 µM against human tumor cells Bel-7402 and K562.