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来自牛心番荔枝的新型生物活性邻位双四氢呋喃类番荔枝内酯

New bioactive adjacent bis-THF annonaceous acetogenins from Annona bullata.

作者信息

Gu Z M, Zeng L, Schwedler J T, Wood K V, McLaughlin J L

机构信息

Department of Medicinal Chemistry and Pharmacognosy, School of Pharmacy and Pharmacal Sciences, Purdue University, West Lafayette, IN 47907, USA.

出版信息

Phytochemistry. 1995 Sep;40(2):467-77. doi: 10.1016/0031-9422(95)00308-t.

Abstract

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.

摘要

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。

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