Colman-Saizarbitoria T, Zambrano J, Ferrigni N R, Gu Z M, Ng J H, Smith D L, McLaughlin J L
Facultad de Farmacia, Universidad Central de Venezuela, Caracas.
J Nat Prod. 1994 Apr;57(4):486-93. doi: 10.1021/np50106a007.
Bioactive Annonaceous acetogenins have been isolated from the EtOH extract of the bark of Xylopia aromatica by bioactivity-directed fractionation using lethality to brine shrimp. These acetogenins include xylopianin [1 , xylopiacin [2], and xylomaticin [3], which are three new mono-tetrahydrofuran ring type acetogenins, in addition to the known compounds, annomontacin, gigantetronenin, gigantetrocin A, and annonacin. Compounds 1 and 2 are unusual in having hydroxylation at C-8; 3 has the same functionalities as annonacin but with 37 carbons instead of 35 carbons. The structures were elucidated by spectral analysis of the parent compounds and/or simple chemical derivatives. These acetogenins showed cytotoxicities, comparable to adriamycin, against three human solid tumor cell lines.
通过以卤虫致死率为导向的生物活性分级分离法,从芳香肉豆蔻的树皮乙醇提取物中分离出了具有生物活性的番荔枝内酯。这些番荔枝内酯包括木番荔枝宁[1]、木番荔枝辛[2]和木番荔枝素[3],它们是三种新的单四氢呋喃环型番荔枝内酯,此外还有已知化合物annonmontacin、gigantetronenin、gigantetrocin A和annonacin。化合物1和2的不寻常之处在于C-8位有羟基化;化合物3与annonacin具有相同的官能团,但有37个碳而不是35个碳。通过对母体化合物和/或简单化学衍生物的光谱分析阐明了其结构。这些番荔枝内酯对三种人类实体瘤细胞系显示出与阿霉素相当的细胞毒性。