Yu Hao-Bing, Yang Fan, Sun Fan, Ma Guo-Yi, Gan Jian-Hong, Hu Wen-Zhen, Han Bing-Nan, Jiao Wei-Hua, Lin Hou-Wen
Laboratory of Marine Drugs, Department of Pharmacy, Changzheng Hospital, Second Military Medical University , 415 Fengyang Road, Shanghai 200003, People's Republic of China.
J Nat Prod. 2014 Sep 26;77(9):2124-9. doi: 10.1021/np500583z. Epub 2014 Sep 11.
Nine new aaptamine derivatives (1-9), together with three known related compounds (10-12), have been isolated from the South China Sea sponge Aaptos aaptos. The structures of all compounds were unambiguously elucidated on the basis of spectroscopic analyses. Structurally, compound 1 possesses a piperidinyl group fused to a demethyl(oxy)aaptamine moiety, whereas compounds 3-6 share an imidazole-fused 1H-benzo[de][1,6]naphthyridin-2(4H)-one skeleton. The cytotoxic activities of the compounds were evaluated against various human cancer cell lines, and compounds 2, 8, 11, and 12 showed potent cytotoxicities against HL60, K562, MCF-7, KB, HepG2, and HT-29 cells, with IC50 values in the range of 0.03 to 8.5 μM.
从中国南海海绵Aaptos aaptos中分离出了9个新的aaptamine衍生物(1-9)以及3个已知的相关化合物(10-12)。所有化合物的结构均通过光谱分析得以明确阐明。在结构上,化合物1具有一个与去甲基(氧基)aaptamine部分稠合的哌啶基,而化合物3-6具有一个咪唑稠合的1H-苯并[de][1,6]萘啶-2(4H)-酮骨架。评估了这些化合物对多种人类癌细胞系的细胞毒性,化合物2、8、11和12对HL60、K562、MCF-7、KB、HepG2和HT-29细胞显示出较强的细胞毒性,IC50值在0.03至8.5μM范围内。