State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, People's Republic of China.
J Nat Prod. 2013 Apr 26;76(4):564-70. doi: 10.1021/np300742d. Epub 2013 Mar 1.
Five new sesquiterpene lactones, racemosalactones A-E (1-5), along with 19 known sesquiterpene latones (6-24), were isolated from the roots of Inula racemosa. Their structures were elucidated by extensive spectroscopic analysis, and the absolute configuration of 2 was deduced from X-ray diffraction analysis. Compounds 1, 6, 8, 10, 12, 14, and 17 exhibited antiproliferative activities with IC50 values ranging from 0.38 to 4.19 μg/mL against human non-small-cell lung cancer A549, hepatocellular carcinoma HepG2, and human fibrosarcoma HT1080 cells. Compounds 6 and 8 exhibited antiproliferative activities against endothelial cells with IC50 values of 2.4 and 2.5 μg/mL, respectively. Furthermore, compounds 6 and 8 both inhibited endothelial cell tube formation at 1.0 μg/mL. A method for the rapid and straightforward preparative-scale isolation of compound 6 from alantolides is described.
从旋覆花根部分离得到五个新的倍半萜内酯化合物,分别命名为 racemosalactones A-E(1-5),以及 19 个已知的倍半萜内酯化合物(6-24)。通过广泛的光谱分析阐明了它们的结构,并通过 X 射线衍射分析推导出了 2 的绝对构型。化合物 1、6、8、10、12、14 和 17 对人非小细胞肺癌 A549、肝癌 HepG2 和人纤维肉瘤 HT1080 细胞表现出抗增殖活性,IC50 值范围为 0.38-4.19μg/mL。化合物 6 和 8 对内皮细胞表现出抗增殖活性,IC50 值分别为 2.4 和 2.5μg/mL。此外,化合物 6 和 8 均能在 1.0μg/mL 浓度下抑制内皮细胞管形成。描述了一种从土木香内酯中快速简便地制备化合物 6 的方法。