Li Chun-Yuan, Ding Wei-Jia, She Zhi-Gang, Lin Yong-Cheng
Department of Applied Chemistry, College of Sciences, South China Agricultural University, Guangzhou 510642, China.
Zhong Yao Cai. 2008 May;31(5):645-7.
The metabolites of a marine streptomyces sp. actinomycete (No. 195-02) were studied and eight compounds were isolated from the fermentation liquid, structures were elucidated by spectroscopy methods as p-hydroxy-benzonitrile (1), 2-methyl-furan-3-carboxylic acid(2), furan-2-carboxylic acid (3), cyclo(Phe-Phe) (4), cyclo(Leu-Ileu) (5), nicotinic acid (6), 2-(1H-indol-3-yl) acetic acid (7) and bis(2-ethylhexyl) phthalate (8). The compounds 1, 3 and 8 were firstly isolated from Streptomyces sp., compounds 4 -7 were firstly found from marine actinomycetes. Coumpouds 4 and 5 evidently inhibited the growth of cancer cell lines hepG2 and hep2 at the concentration of 50 microg/ml.
对一株海洋链霉菌属放线菌(编号195 - 02)的代谢产物进行了研究,从发酵液中分离出8种化合物,通过光谱法鉴定其结构分别为对羟基苯甲腈(1)、2 - 甲基呋喃 - 3 - 羧酸(2)、呋喃 - 2 - 羧酸(3)、环(苯丙 - 苯丙)(4)、环(亮 - 异亮)(5)、烟酸(6)、2 -(1H - 吲哚 - 3 - 基)乙酸(7)和邻苯二甲酸二(2 - 乙基己基)酯(8)。化合物1、3和8首次从链霉菌属中分离得到,化合物4 - 7首次从海洋放线菌中发现。化合物4和5在浓度为50微克/毫升时明显抑制癌细胞系hepG2和hep2的生长。