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

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
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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.

Supporting Information

 
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