Ahmed Atallah F, Dai Chang-Feng, Kuo Yao-Haur, Sheu Jyh-Horng
Department of Marine Resources, National Sun Yat-Sen University, Kaohsiung 804, Taiwan, ROC.
Steroids. 2003 Apr;68(4):377-81. doi: 10.1016/s0039-128x(03)00036-9.
A novel steroid, 1alpha,3beta,5beta-trihydroxy-24-methylenecholestan-6-one (gibberoketosterol) (1), along with four known steroids, was isolated from the lipophilic extracts of a Taiwanese soft coral Sinularia gibberosa. The structure of the new metabolite was determined on the basis of extensive spectral analyses and chemical reaction. The relative stereochemistry of gibberoketosterol was established by the NOESY experiments and analysis of the pyridine-induced deshielding effect of the axial hydroxy groups. Gibberoketosterol is the first example of 1alpha,3beta,5beta-trihydroxy-6-oxosteroids isolated from natural sources and was found to exhibit a moderate cytotoxicity against the growth of Hepa59T/VGH cancer cells.
从台湾软珊瑚中华软珊瑚(Sinularia gibberosa)的亲脂性提取物中分离出一种新型甾体化合物1α,3β,5β-三羟基-24-亚甲基胆甾烷-6-酮(gibberoketosterol)(1)以及四种已知甾体化合物。通过广泛的光谱分析和化学反应确定了新代谢产物的结构。通过NOESY实验以及对轴向羟基吡啶诱导的去屏蔽效应的分析确定了gibberoketosterol的相对立体化学结构。Gibberoketosterol是从天然来源分离出的1α,3β,5β-三羟基-6-氧代甾体的首个实例,并且发现其对Hepa59T/VGH癌细胞的生长表现出中等细胞毒性。