Copper(I) oxide nanoparticles catalyzed click chemistry based synthesis of melampomagnolide B-triazole conjugates and their anti-cancer activities

被引:32
作者
Ding, Yahui [1 ,2 ]
Guo, Hongyu [1 ,2 ]
Ge, Weizhi [1 ,2 ]
Chen, Xinyi [1 ,2 ]
Li, Shengzu [1 ,2 ]
Wang, Mengmeng [3 ]
Chen, Yue [1 ,2 ]
Zhang, Quan [1 ,2 ]
机构
[1] Nankai Univ, Coll Pharm, State Key Lab Med Chem Biol, Haihe Educ Pk,38 Tongyan Rd, Tianjin 300353, Peoples R China
[2] Nankai Univ, Tianjin Key Lab Mol Drug Res, Haihe Educ Pk,38 Tongyan Rd, Tianjin 300353, Peoples R China
[3] Accendatech Co Ltd, Tianjin 300384, Peoples R China
基金
中国国家自然科学基金;
关键词
Melampomagnolide B; Parthenolide; Click chemistry; Copper(I) oxide nanoparticles; Anti-cancer activity; CANCER STEM-CELLS; ACUTE MYELOGENOUS LEUKEMIA; SESQUITERPENE LACTONES; AGENTS; PARTHENOLIDE; 1,2,3-TRIAZOLES; DERIVATIVES; RESISTANCE; DISCOVERY; IMPACT;
D O I
10.1016/j.ejmech.2018.06.058
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of thirty one melampomagnolide B-triazole conjugates was synthesized via Copper(I) oxide nanoparticles catalyzed click chemistry. These conjugates were evaluated for their anti-cancer activities against a panel of five human cancer cell lines. The most active compound 6e showed high activity against H0116 cell line with IC50 value of 0.43 mu M, which demonstrated 11.5-fold improvement compared to that of the parent compound melampomagnolide B (IC50 = 4.93 mu M). Compound 6e showed significant efficacy of inducing apoptosis, inhibiting proliferation and migration of HCT116 cells. The preliminary molecular mechanism of 6e was also investigated. On the base of these results, compound 6e might be considered as a promising candidate for further evaluation as a potential anti-cancer drug. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:216 / 229
页数:14
相关论文
共 36 条
[1]   Click Chemistry: 1,2,3-Triazoles as Pharmacophores [J].
Agalave, Sandip G. ;
Maujan, Suleman R. ;
Pore, Vandana S. .
CHEMISTRY-AN ASIAN JOURNAL, 2011, 6 (10) :2696-2718
[2]   Identification of a melampomagnolide B analog as a potential lead molecule for treatment of acute myelogenous leukemia [J].
Albayati, Zaineb A. F. ;
Janganati, Venumadhav ;
Chen, Zheng ;
Ponder, Jessica ;
Breen, Philip J. ;
Jordan, Craig T. ;
Crooks, Peter A. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2017, 25 (03) :1235-1241
[3]   Cancer stem cells: problems for therapy? [J].
Alison, Malcolm R. ;
Lim, Susan M. L. ;
Nicholson, Linda J. .
JOURNAL OF PATHOLOGY, 2011, 223 (02) :147-161
[4]   Indole carboxylic acid esters of melampomagnolide B are potent anticancer agents against both hematological and solid tumor cells [J].
Bommagani, Shobanbabu ;
Ponder, Jessica ;
Penthala, Narsimha R. ;
Janganati, Venumadhav ;
Jordan, Craig T. ;
Borrelli, Michael J. ;
Crooks, Peter A. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 136 :393-405
[5]   Sesquiterpenoids Lactones: Benefits to Plants and People [J].
Chadwick, Martin ;
Trewin, Harriet ;
Gawthrop, Frances ;
Wagstaff, Carol .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (06) :12780-12805
[6]  
Clarke Michael F, 2006, Cancer Res, V66, P9339, DOI 10.1158/0008-5472.CAN-06-3126
[7]   Medicinal attributes of 1,2,3-triazoles: Current developments [J].
Dheer, Divya ;
Singh, Virender ;
Shankar, Ravi .
BIOORGANIC CHEMISTRY, 2017, 71 :30-54
[8]  
ELFERALY FS, 1984, PHYTOCHEMISTRY, V23, P2372
[9]   The role of oxidative stress in anticancer activity of sesquiterpene lactones [J].
Gach, Katarzyna ;
Dugosz, Angelika ;
Janecka, Anna .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2015, 388 (05) :477-486
[10]   Parthenolide: from plant shoots to cancer roots [J].
Ghantous, Akram ;
Sinjab, Ansam ;
Herceg, Zdenko ;
Darwiche, Nadine .
DRUG DISCOVERY TODAY, 2013, 18 (17-18) :894-905