Dipartimento di Farmacia, Università di Napoli 'Federico II', Via D. Montesano 49, 80131 Napoli, Italy.
Bioorg Med Chem. 2013 Sep 1;21(17):5332-8. doi: 10.1016/j.bmc.2013.06.015. Epub 2013 Jun 15.
Chemical investigation of an Indonesian specimen of Theonella swinhoei afforded the new dimeric macrolides isoswinholide B (5) and swinholide K (6), along with the known swinholides A (1), B (2) and D (3) and isoswinholide A (4). Isoswinholide B showed an unprecedented 21/19' lactonization pattern, while swinholide K included an sp(2) methylene attached at C-4 and an additional oxymethine group at C-5, whose configuration has been determined through application of J-based configuration analysis. The isolated swinholides (1-6), with the exception of isoswinholide B, showed a cytotoxic activity on HepG2 (hepatocarcinoma cell line) in the nanomolar range.
对印度尼西亚标本 Theonella swinhoei 的化学研究得到了新的二聚大环内酯类化合物异swinholide B(5)和 swinholide K(6),以及已知的 swinholides A(1)、B(2)和 D(3)和异swinholide A(4)。异swinholide B 表现出前所未有的 21/19'内酯化模式,而 swinholide K 则在 C-4 处包含一个 sp(2)亚甲基和 C-5 处的额外氧亚甲基,其构型通过应用 J 基于构型分析确定。除了异swinholide B 之外,分离得到的 swinholides(1-6)在纳摩尔范围内对 HepG2(肝癌细胞系)表现出细胞毒性活性。