Li Guoqiang, Deng Zhiwei, Guan Huashi, van Ofwegen Leen, Proksch Peter, Lin Wenhan
State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100083, China.
Steroids. 2005 Jan;70(1):13-8. doi: 10.1016/j.steroids.2004.09.003. Epub 2004 Dec 8.
Fifteen steroids were isolated from the soft coral Dendronephthya sp., of which five are determined as new compounds, namely (22E)-3-O-beta-formylcholest-5,22-diene (1), (22E)-3-O-beta-formyl-24-methyl-cholest-5,22-diene (2), 2-ethoxycarbonyl-2-beta-hydroxy-A-nor-cholest-5-ene-4-one (3), (22E)-2-ethoxycarbonyl-2-beta-hydroxy-A-nor-cholest-5,22-diene-4-one (4), and (22E)-2-ethoxycarbonyl-2-beta-hydroxy-24-mthyl-A-nor-cholest-5,22-diene-4- one (5). 1 and 2 belonged to 3-O-formylated cholesterol analogues, and 3 to 5 are unique ring A-contracted steroids. Their structures were elucidated by extensive 2D NMR in association with IR, MS analysis.
从软珊瑚Dendronephthya sp.中分离出15种甾体化合物,其中5种被确定为新化合物,即(22E)-3-O-β-甲酰基胆甾-5,22-二烯(1)、(22E)-3-O-β-甲酰基-24-甲基胆甾-5,22-二烯(2)、2-乙氧羰基-2-β-羟基-A-降胆甾-5-烯-4-酮(3)、(22E)-2-乙氧羰基-2-β-羟基-A-降胆甾-5,22-二烯-4-酮(4)和(22E)-2-乙氧羰基-2-β-羟基-24-甲基-A-降胆甾-5,22-二烯-4-酮(5)。1和2属于3-O-甲酰化胆固醇类似物,3至5是独特的A环缩合甾体。通过广泛的二维核磁共振结合红外光谱、质谱分析确定了它们的结构。