Takemoto Kenji, Kamisuki Shinji, Chia Pei Thing, Kuriyama Isoko, Mizushina Yoshiyuki, Sugawara Fumio
Department of Applied Biological Science, Tokyo University of Science , Noda, Chiba 278-8510, Japan.
J Nat Prod. 2014 Sep 26;77(9):1992-6. doi: 10.1021/np500175j. Epub 2014 Aug 28.
New dihydronaphthoquinone derivatives, karuquinone A (1), karuquinone B (2), and karuquinone C (3), were isolated from a fungal culture broth of Fusarium solani. The structures were determined by interpretation of spectroscopic data (1D/2D NMR, MS, and IR). Three known compounds, javanicin (4), 2,3-dihydro-5-hydroxy-8-methoxy-2,4-dimethylnaphtho[1,2-b]furan-6,9-dione (5), and 5-hydroxydihydrofusarubin C (6), were also isolated. The six isolated compounds were tested for cytotoxicity against three human cancer cell lines and a human umbilical vein endothelial cell (HUVEC) line. Of these, karuquinone A exhibited the strongest cytotoxic activity. Karuquinone B did not affect the proliferation of the cancer cell lines but did inhibit the proliferation of HUVEC. Additionally, we demonstrated that karuquinone A induces apoptosis in cancer cells through the generation of reactive oxygen species (ROS).
从茄病镰刀菌的真菌培养液中分离出了新的二氢萘醌衍生物,即卡鲁醌A(1)、卡鲁醌B(2)和卡鲁醌C(3)。通过对光谱数据(一维/二维核磁共振、质谱和红外光谱)的解析确定了其结构。还分离出了三种已知化合物,即爪哇尼辛(4)、2,3 - 二氢 - 5 - 羟基 - 8 - 甲氧基 - 2,4 - 二甲基萘并[1,2 - b]呋喃 - 6,9 - 二酮(5)和5 - 羟基二氢镰孢菌素C(6)。对分离得到的这六种化合物针对三种人类癌细胞系和一种人脐静脉内皮细胞(HUVEC)系进行了细胞毒性测试。其中,卡鲁醌A表现出最强的细胞毒性活性。卡鲁醌B不影响癌细胞系的增殖,但确实抑制了HUVEC的增殖。此外,我们证明卡鲁醌A通过产生活性氧(ROS)诱导癌细胞凋亡。