Design, synthesis and biological evaluation of novel C-29 carbamate celastrol derivatives as potent and selective cytotoxic compounds

被引:28
作者
Figueiredo, Sandra A. C. [1 ,2 ]
Salvador, Jorge A. R. [1 ,2 ]
Cortes, Roldan [3 ]
Cascante, Marta [3 ]
机构
[1] Univ Coimbra, Lab Pharmaceut Chem, Fac Pharm, P-3000548 Coimbra, Portugal
[2] Ctr Neurosci & Cell Biol, Coimbra, Portugal
[3] Univ Barcelona, Dept Biochem & Mol Biomed, Fac Biol, Inst Biomed, Diagonal 643, E-08028 Barcelona, Spain
关键词
Celastrol; Triterpenes; Carbamates; Cytotoxicity; Apoptosis; Drug synergy; ANTITUMOR-ACTIVITY; CANCER-CELLS; ASIATIC ACID; ANTICANCER; CARBOPLATIN; HSP90-CDC37; INHIBITION; PACLITAXEL; MECHANISM; MOIETY;
D O I
10.1016/j.ejmech.2017.08.058
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Celastrol and its derivatives have been reported for their potent anticancer activity. Among other celastrol analogues, novel carbamate derivatives were designed and synthesised, and their biological activity on the viability of human cancer cell lines was evaluated. Additionally, a preliminary structure activity relationship study was conducted. Derivative 18 showed the highest activity on cancer cell viability, combined with the best selectivity between malignant cells and non-malignant fibroblasts. Preliminary mechanistic studies of its anti-tumour action indicated that compound 18 has an anti proliferative effect on SKOV-3 human ovarian cancer cells (IC50 = 0.54 mu M). The results also suggested that its potent anticancer activity is mediated by apoptosis, and that this process was mainly the result of the activation of the extrinsic apoptotic pathway. Moreover, our results demonstrated the potential of derivative 18 as a new agent for combinatorial drug therapy for ovarian cancer. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:836 / 848
页数:13
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