Research Center for Marine Drugs, School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai 200433, China.
Mar Drugs. 2013 Mar 11;11(3):775-87. doi: 10.3390/md11030775.
Seven new polyoxygenated steroids (1-7) were isolated together with seven known analogues (8-14) from the South China Sea soft coral, Sarcophyton sp. The structures of the new compounds were identified on the basis of extensive spectroscopic analysis and comparison with reported data. All the steroids are characterized with 3β,5α,6β-hydroxy moiety, displaying carbon skeletons of cholestane, ergostane, gorgostane and 23,24-dimethyl cholestane. In the in vitro bioassay, metabolites exhibited different levels of antimicrobial activity against bacterial species Escherichia coli and Bacillus megaterium, and fungal species Microbotryum violaceum and Septoria tritici. No inhibition was detected towards microalga Chlorella fusca. Preliminary structure-activity analysis suggests that the 11α-acetoxy group may increase both antibacterial and antifungal activities. The terminal-double bond and the cyclopropane moiety at the side chain may also contribute to the bioactivity.
从南海软珊瑚 Sarcophyton sp. 中分离得到了 7 种新的多氧化甾体(1-7)和 7 种已知类似物(8-14)。根据广泛的光谱分析和与报道数据的比较,确定了新化合物的结构。所有甾体都具有 3β,5α,6β-羟基部分,呈现胆甾烷、麦角甾烷、高利甾烷和 23,24-二甲基胆甾烷的碳骨架。在体外生物测定中,代谢产物对细菌物种大肠杆菌和巨大芽孢杆菌以及真菌物种紫色小球藻和小麦叶斑病菌显示出不同水平的抗菌活性。对微藻 Chlorella fusca 没有抑制作用。初步的结构-活性分析表明,11α-乙酰氧基可能增加抗菌和抗真菌活性。侧链末端双键和环丙烷部分也可能对生物活性有贡献。