具有抗肿瘤活性的姜黄素衍生物研究进展

被引:13
作者
张欢 [1 ]
房雷 [2 ]
苟少华 [2 ]
陈莉 [1 ]
机构
[1] 中国药科大学天然药物化学教研室
[2] 东南大学药物化学研究中心
关键词
姜黄素; 结构修饰; 构效关系; 生物利用度;
D O I
暂无
中图分类号
R285 [中药药理学];
学科分类号
100806 [中药药理学];
摘要
姜黄素是一种具有抗肿瘤、抗阿尔茨海默病、抗氧化、抗炎、抗病毒等多种生物活性的天然多酚,但其存在生物利用度低、水溶性较差等缺点,使其临床应用受到限制。基于此,研究人员对姜黄素展开了大量的结构改造工作,以期能改善其生物活性及成药性。综述了具有抗肿瘤活性的姜黄素衍生物的研究进展,旨在为相关药物的研发提供参考。
引用
收藏
页码:36 / 45
页数:10
相关论文
共 22 条
[1]
Exploring pyrimidine-substituted curcumin analogues: Design; synthesis and effects on EGFR signaling.[J].Peiju Qiu;Lingling Xu;Lei Gao;Meng Zhang;Shixi Wang;Sheng Tong;Yue Sun;Lijuan Zhang;Tao Jiang.Bioorganic & Medicinal Chemistry.2013,
[2]
2a, a novel curcumin analog, sensitizes cisplatin-resistant A549 cells to cisplatin by inhibiting thioredoxin reductase concomitant oxidative stress damage [J].
Zhou, Binhua ;
Huang, Jianing ;
Zuo, Yinglin ;
Li, Baojian ;
Guo, Qiang ;
Cui, Baicheng ;
Shao, Weiyan ;
Du, Jun ;
Bu, Xianzhang .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2013, 707 (1-3) :130-139
[3]
Design and synthesis of dimethylaminomethyl-substituted curcumin derivatives/analogues: Potent antitumor and antioxidant activity, improved stability and aqueous solubility compared with curcumin [J].
Fang, Xubin ;
Fang, Lei ;
Gou, Shaohua ;
Cheng, Lin .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (05) :1297-1301
[4]
Curcumin: a natural substance with potential efficacy in Alzheimer’s disease.[J].Pamela Potter.Journal of Experimental Pharmacology.2013, defa
[5]
Synthesis, characterization, and antitumour studies of some curcuminoid analogues and their aluminum complexes [J].
John, Valapatukutikadan Davis ;
Ummathur, Muhammed Basheer ;
Krishnankutty, Krishnannair .
JOURNAL OF COORDINATION CHEMISTRY, 2013, 66 (09) :1508-1518
[6]
Synthesis; cytotoxicity of new 4-arylidene curcumin analogues and their multi-functions in inhibition of both NF-κB and Akt signalling.[J].Yinglin Zuo;Jianing Huang;Binhua Zhou;Shuni Wang;Weiyan Shao;Cuige Zhu;Li Lin;Gesi Wen;Hongyang Wang;Jun Du;Xianzhang Bu.European Journal of Medicinal Chemistry.2012,
[7]
Reproductive effects of a pegylated curcumin [J].
Murphy, Caitlin J. ;
Tang, Huadong ;
Van Kirk, Edward A. ;
Shen, Youqing ;
Murdoch, William J. .
REPRODUCTIVE TOXICOLOGY, 2012, 34 (01) :120-124
[8]
Design, synthesis, synergistic antimicrobial activity and cytotoxicity of 4-aryl substituted 3,4-dihydropyrimidinones of curcumin [J].
Lal, Jaggi ;
Gupta, S. K. ;
Thavaselvam, D. ;
Agarwal, D. D. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 22 (08) :2872-2876
[9]
T63; a new 4-arylidene curcumin analogue; induces cell cycle arrest and apoptosis through activation of the reactive oxygen species–FOXO3a pathway in lung cancer cells.[J].Hao Liu;Bin-Hua Zhou;Xu Qiu;Hong-Sheng Wang;Fan Zhang;Rui Fang;Xian-Feng Wang;Shao-Hui Cai;Jun Du;Xian-Zhang Bu.Free Radical Biology and Medicine.2012, 12
[10]
Binding of isoxazole and pyrazole derivatives of curcumin with the activator binding domain of novel protein kinase C [J].
Das, Joydip ;
Pany, Satyabrata ;
Panchal, Shyam ;
Majhi, Anjoy ;
Rahman, Ghazi M. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2011, 19 (21) :6196-6202