Department of Pharmacognosy and Phytochemistry, Meiji Pharmaceutical University, Noshio 2-522-1, Kiyose-shi, Tokyo 204-8588, Japan.
J Nat Prod. 2011 Jul 22;74(7):1645-9. doi: 10.1021/np200108h. Epub 2011 Jun 30.
Three new diterpenes, myrocin D (1), libertellenone E (2), and libertellenone F (3), and a new isocoumarin, decarboxyhydroxycitrinone (4), were isolated from the marine fungus Arthrinium sacchari, together with three known compounds (5-7). The structures of 1-4 were elucidated from spectroscopic data (NMR, MS, IR), and the absolute configurations of 1-3 were determined by X-ray diffraction analysis. The antiangiogenic activity of these compounds was evaluated by measuring their antiproliferation effects on human umbilical vein endothelial cells (HUVECs) and human umbilical artery endothelial cells (HUAECs). Compounds 4-7 showed inhibitory activity.
三种新的二萜类化合物,即 myrocin D(1)、libertellenone E(2)和 libertellenone F(3),以及一种新的异香豆素化合物 decarboxyhydroxycitrinone(4),从海洋真菌 Arthrinium sacchari 中分离得到,同时还分离得到了三种已知化合物(5-7)。通过光谱数据(NMR、MS、IR)解析了 1-4 的结构,并通过 X 射线衍射分析确定了 1-3 的绝对构型。通过测量对人脐静脉内皮细胞(HUVEC)和人脐动脉内皮细胞(HUAEC)的增殖抑制作用来评估这些化合物的抗血管生成活性。化合物 4-7 显示出抑制活性。