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作 者:朱峰[1] 林永成[2] 王军[3] 周世宁[3] Vrijmoed L LP
机构地区:[1]佛山科学技术学院化学与化工系,广东佛山528000 [2]中山大学化学与化学工程学院,广东广州510275 [3]中山大学生命科学学院,广东广州510275 [4]香港城市大学生物学与化学系
出 处:《化学研究与应用》2005年第6期790-792,共3页Chemical Research and Application
基 金:国家863计划资助项目(2001AA624010);广东自然科学基金资助项目(04300674);广东省科技计划资助项目(2004B30101017)
摘 要:Two metabolites(A and B) were isolated from a mangrove endophytic fungus Stysanus like sp.(#2492) from the South China Sea.Their structures were elucidated by spectral data as N-(2’-hydroxytetracosyl)-2-amino1,3,4-trihydroxyoctadecane(A) and γ-stearolactone(B).In the primary bioassay,compound B did not exhibit significant inhibitory activity to DNA topoisomerase hTOP Ⅰ,and also had no significant inhibitory activity to tumor cell lines Bel-7402 and NCIH-460.It was the first report that γ-stearolactone(B) isolated from marine fungus as natural product.Two metabolites( A and B) were isolated from a mangrove endophytic fungus Stysanus like sp. (#2492) from the South China Sea. Their structures were elucidated by spectral data as N - (2' - hydroxytetracosyl) -2 - amino - 1,3,4 - trihydroxyoctadecane (A) and γ-stearolactone (B). In the primary bioassay, compound B did not exhibit significant inhibitory activity to DNA topoisomerase hTOP Ⅰ , and also had no significant inhibitory activity to tumor cell lines Bel - 7402 and NCIH - 460. It was the first report that γ - stearolactone (B) isolated from marine fungus as natural product.
关 键 词:海洋真菌 代谢产物 N-(1’-羟甲基-2’ 3’-二羟基)十七烷基-2-羟基二十四碳酰胺 γ-硬脂酸内酯 生理活性
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