Gu Z M, Zeng L, Schwedler J T, Wood K V, McLaughlin J L
Department of Medicinal Chemistry and Pharmacognosy, School of Pharmacy and Pharmacal Sciences, Purdue University, West Lafayette, IN 47907, USA.
Phytochemistry. 1995 Sep;40(2):467-77. doi: 10.1016/0031-9422(95)00308-t.
Five new adjacent bis-THF annonaceous acetogenins, 32-hydroxybullatacin, 31-hydroxybullatacin, 30-hydroxybullatacin, and (2,4-cis and trans)-28-hydroxybullatacinones, were isolated from the ethanolic extract of the bark of Annona bullata Rich. (Annonaceae). The absolute configurations of the above five compounds, as well as those of (2,4-cis and trans)-32-, 31-, and 30-hydroxybullatacinones and (2,4-cis and trans)-bulladecinones, previously isolated from the same extract, were defined by the application of the advanced Mosher ester [methoxy(trifluoromethyl)phenyl acetate or MTPA] methodology. The determination of the absolute configuration of C-20 of (2,4-cis and trans)-bulladecinones to be S supports our hypothesis that the cyclization of the THF rings of (2,4-cis and trans)-bulladecinones starts from C-12 (the right side). The first five compounds listed above showed potent bioactivities in the brine shrimp lethality test (BST) and among six human solid tumour cell lines.
从番荔枝科植物钝叶番荔枝(Annona bullata Rich.)树皮的乙醇提取物中分离出5种新的相邻双四氢呋喃番荔枝内酯,分别为32-羟基bullatacin、31-羟基bullatacin、30-羟基bullatacin以及(2,4-顺式和反式)-28-羟基bullatacinone。通过采用先进的莫舍尔酯[甲氧基(三氟甲基)苯基乙酸酯或MTPA]方法,确定了上述5种化合物以及之前从同一提取物中分离出的(2,4-顺式和反式)-32-、31-和30-羟基bullatacinone以及(2,4-顺式和反式)-bulladecinone的绝对构型。(2,4-顺式和反式)-bulladecinone的C-20绝对构型确定为S,这支持了我们的假设,即(2,4-顺式和反式)-bulladecinone的四氢呋喃环的环化从C-12(右侧)开始。上述前5种化合物在卤虫致死试验(BST)和6种人类实体瘤细胞系中显示出强大的生物活性。