Li Jiao, Li Cui, Riccio Raffaele, Lauro Gianluigi, Bifulco Giuseppe, Li Tie-Jun, Tang Hua, Zhuang Chun-Lin, Ma Hao, Sun Peng, Zhang Wen
Research Center for Marine Drugs, School of Pharmacy, Second Military Medical University, 325 Guo-He Road, Shanghai 200433, China.
Science and Research Laboratory, Longhua Hosptial, Shanghai University of Traditional Chinese Medicine, 725 South Wanping Road, Shanghai 200032, China.
Mar Drugs. 2017 May 3;15(5):129. doi: 10.3390/md15050129.
Simplextone E (), a new metabolite of polyketide origin, was isolated with eight known analogues (-) from the South China Sea sponge sp. The relative configuration of the new compound was elucidated by a detailed analysis of the spectroscopic data and quantum mechanical calculation of NMR chemical shifts, aided by the newly reported DP4+ approach. Its absolute configuration was determined by the TDDFT/ECD calculation. Simplextone E () is proven to be one of the isomers of simplextone D. The absolute configuration at C-8 in alkyl chain of plakortone Q () was also assigned based on the NMR calculation. In the preliminary in vitro bioassay, compounds and showed a selective growth inhibitory activity against HCT-116 human colon cancer cells with IC values of 8.3 ± 2.4 and 8.4 ± 2.3 μM, corresponding to that of the positive control, adriamycin (IC 4.1 μM). The two compounds also showed selective activities towards MCF-7 human breast cancer and K562 human erythroleukemia cells while compound only displayed weak activity against K562 cells.
Simplextone E()是一种新的聚酮类代谢产物,与8种已知类似物(-)一起从中国南海海绵 sp.中分离得到。通过对光谱数据的详细分析以及借助新报道的DP4 +方法对NMR化学位移进行量子力学计算,阐明了新化合物的相对构型。通过TDDFT / ECD计算确定了其绝对构型。已证明Simplextone E()是Simplextone D的异构体之一。基于NMR计算,还确定了Plakortone Q()烷基链中C-8处的绝对构型。在初步的体外生物测定中,化合物 和 对HCT-116人结肠癌细胞表现出选择性生长抑制活性,IC值分别为8.3±2.4和8.4±2.3μM,与阳性对照阿霉素(IC 4.1μM)相当。这两种化合物对MCF-7人乳腺癌和K562人红白血病细胞也表现出选择性活性,而化合物 仅对K562细胞表现出微弱活性。