Suppr超能文献

南海海绵Plakortis sp.中聚酮化合物的化学结构及其对肿瘤细胞的选择性生长抑制活性

Chemistry and Selective Tumor Cell Growth Inhibitory Activity of Polyketides from the South China Sea Sponge Plakortis sp.

作者信息

Li Jiao, Li Cui, Riccio Raffaele, Lauro Gianluigi, Bifulco Giuseppe, Li Tie-Jun, Tang Hua, Zhuang Chun-Lin, Ma Hao, Sun Peng, Zhang Wen

机构信息

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.

出版信息

Mar Drugs. 2017 May 3;15(5):129. doi: 10.3390/md15050129.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b680/5450535/d8a9956e5cbc/marinedrugs-15-00129-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验