Liu Yang, Kurtán Tibor, Yun Wang Chang, Han Lin Wen, Orfali Raha, Müller Werner Eg, Daletos Georgios, Proksch Peter
Institute of Pharmaceutical Biology and Biotechnology, Heinrich Heine University, Duesseldorf, Germany.
Key Laboratory of Marine Drugs, The Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, People's Republic of China.
J Antibiot (Tokyo). 2016 Sep;69(9):702-6. doi: 10.1038/ja.2016.11. Epub 2016 Feb 24.
A new cytotoxic viriditoxin derivative, cladosporinone (1), along with the known viriditoxin (2) and two viriditoxin derivatives (3 and 4) were obtained from the fungus Cladosporium cladosporioides isolated from the sediment of a hypersaline lake in Egypt. The structure of the new compound (1) was determined by 1D and 2D NMR measurements as well as by high-resolution ESIMS and electronic circular dichroism spectroscopy. All isolated compounds were studied for their cytotoxicity against the murine lymphoma cell line L5187Y and for their antibiotic activity against several pathogenic bacteria. Viriditoxin (2) was the most active compound in both bioassays. Compound 1 also exhibited strong cytotoxicity against the murine lymphoma cell line L5187Y with an IC50 value of 0.88 μm, whereas its antibiotic activity was weak.
从埃及一个高盐湖沉积物中分离出的枝孢菌中获得了一种新的细胞毒性绿胶霉素衍生物枝孢菌素(1),以及已知的绿胶霉素(2)和两种绿胶霉素衍生物(3和4)。通过一维和二维核磁共振测量以及高分辨率电喷雾电离质谱和电子圆二色光谱确定了新化合物(1)的结构。研究了所有分离出的化合物对小鼠淋巴瘤细胞系L5187Y的细胞毒性以及对几种病原菌的抗菌活性。在这两种生物测定中,绿胶霉素(2)是活性最强的化合物。化合物1对小鼠淋巴瘤细胞系L5187Y也表现出很强的细胞毒性,IC50值为0.88μm,但其抗菌活性较弱。