Department of Natural Drugs, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences, Brno, Czech Republic.
Planta Med. 2010 Oct;76(15):1672-7. doi: 10.1055/s-0030-1249861. Epub 2010 May 10.
Using exhaustive chromatographic separation we have isolated (-)-tigloyl-deangeloyl-gomisin F as a novel dibenzocyclooctadiene lignan from schisandra chinensis. With the help of HPLC, we further isolated (+)-schisandrin, (+)-deoxyschisandrin, (+)-γ-schisandrin, (-)-gomisin J, (+)-gomisin A, (-)-gomisin N, (-)-tigloyl-gomisin P, (-)-wuweizisu C, (-)-gomisin D, rubrisandrin A, (-)-gomisin G, (+)-gomisin K (3) and (-)-schisantherin C. A full NMR description of (-)-schisantherin C was carried out with the aim to confirm previous reports of its structure. Compounds isolated were identified on the basis of UV, IR, (1)H- and (13)C-NMR and MS. The cytotoxicity of lignans was tested for the BY-2 cell line alone and as a synergistic effect with the cytotoxic agent camptothecin. Lignans showed various toxicity and synergistic and antagonistic effects on camptothecin-induced cytotoxicity. Cytotoxicity against colon cancer cell line LoVo was also tested.
采用彻底的色谱分离方法,我们从五味子中分离出(-)-tigloyl-deangeloyl-gomisin F,这是一种新型的二苯并环辛二烯木脂素。借助 HPLC,我们进一步分离出(+)-五味子素、(+)-去氧五味子素、(+)-γ-五味子素、(-)-gomisin J、(+)-gomisin A、(-)-gomisin N、(-)-tigloyl-gomisin P、(-)-wuweizisu C、(-)-gomisin D、rubrisandrin A、(-)-gomisin G、(+)-gomisin K(3)和(-)-schisantherin C。(-)-schisantherin C 的完整 NMR 描述是为了证实其结构的先前报道。根据 UV、IR、(1)H 和(13)C-NMR 和 MS 对分离出的化合物进行了鉴定。木脂素的细胞毒性仅针对 BY-2 细胞系进行了测试,并与细胞毒性剂喜树碱进行了协同作用测试。木脂素对喜树碱诱导的细胞毒性表现出不同的毒性以及协同和拮抗作用。还测试了对结肠癌 LoVo 细胞系的细胞毒性。