Department of Chemistry, National Cheng Kung University , Tainan 70101, Taiwan.
J Nat Prod. 2014 May 23;77(5):1215-23. doi: 10.1021/np500088u. Epub 2014 May 5.
Eight new carbazole alkaloids, claulamines C (1), D (2), and E (5) and clausenalines B-F (3, 4, 6-8), four new coumarins, clausemarins A-D (9-12), and 43 known compounds were isolated from the roots of Clausena lansium. The structures of the new compounds were established on the basis of 2D-NMR spectroscopic analysis, and their absolute configurations were established from their ECD spectra. The configuration of wampetin was revised as E using a NOESY experiment. Most of the isolated compounds were evaluated for their potential anti-inflammatory activity. The results showed that compounds 9, 13-18, and 20-22 exhibited strong inhibition of superoxide anion generation with IC50 values ranging from 1.9 to 8.4 μM, while compounds 18, 19, and 21 inhibited elastase release with IC50 values in the range from 2.0 to 6.9 μM.
从枳椇根部分离得到了 8 个新的咔唑生物碱,克劳胺 C(1)、D(2)和 E(5)以及克劳森胺 B-F(3、4、6-8),4 个新的香豆素,克劳森玛琳 A-D(9-12)和 43 种已知化合物。新化合物的结构是基于 2D-NMR 光谱分析确定的,其绝对构型是根据它们的 ECD 光谱确定的。通过 NOESY 实验将 wampetin 的构型修订为 E。对分离得到的大部分化合物进行了潜在抗炎活性评价。结果表明,化合物 9、13-18 和 20-22 对超氧阴离子生成具有很强的抑制作用,IC50 值范围为 1.9-8.4 μM,而化合物 18、19 和 21 对弹性蛋白酶释放的抑制作用,IC50 值范围为 2.0-6.9 μM。