Design and synthesis of pregnenolone/2-cyanoacryloyl conjugates with dual NF-kappa B inhibitory and anti-proliferative activities
文献类型： 外文期刊
作者： Song, Jia-Li 1 ; Zhang, Juan 2 ; Liu, Chang-Liang 4 ; Liu, Chao; Zhu, Kong-Kai 1 ; Yang, Fei-Fei 1 ; Liu, Xi-Gong 1 ; Longo, Joao Paulo Figueiro 2 ; Muehlmann, Luis Alexandre 2 ; Azevedo, Ricardo Bentes 3 ; Zhang, Yu-Ying 1 ; Guo, Yue-Wei; Jiang, Cheng-Shi 1 ; Zhang, Hua 1 ;
作者机构： 1.Univ Jinan, Sch Biol Sci & Technol, Jinan 250022, Shandong, Peoples R China
2.Univ Brasilia, Fac Ceilandia, BR-72220275 Brasilia, DF, Brazil
3.Univ Brasilia, Inst Biol Sci, BR-70910900 Brasilia, DF, Brazil
4.Harvard Med Sch, Dept Neurobiol, Bost
关键词： Pregnenolone; NF-kappa B; 2-Cyanoacryloyl; Michael acceptor; Anti-proliferative activity
期刊名称：BIOORGANIC & MEDICINAL CHEMISTRY LETTERS （ 影响因子：2.823； 五年影响因子：2.677 ）
ISSN： 0960-894X
年卷期： 2017 年 27 卷 20 期
页码：
收录情况： SCI
摘要： Twenty-five novel pregnenolone/2-cyanoacryloyl conjugates (6-30) were designed and prepared, with the aim of developing novel anticancer drugs with dual NF-kappa B inhibitory and anti-proliferative activities. Compounds 22 and 27-30 showed inhibition against TNF-alpha-induced NF-kappa B activation in luciferase assay, which was confirmed by Western blotting. Among them, compound 30 showed potent NF-kappa B inhibitory activity (IC50 = 2.5 mu M) and anti-proliferative against MCF-7, A549, H157, and HL-60 cell lines (IC50 = 6.5-36.2 mu M). The present study indicated that pregnenolone/2-cyanoacryloyl conjugate I can server as a novel scaffold for developing NF-kappa B inhibitors and anti-proliferative agents in cancer chemotherapy. (C) 2017 Elsevier Ltd. All rights reserved.
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