Synthesis, structure elucidation and biological evaluation of triple bridged dinuclear copper(II) complexes as anticancer and antioxidant/anti-inflammatory agents

被引:16
作者
Boulsourani, Z. [1 ]
Katsamakas, S. [2 ]
Geromichalos, G. D. [3 ]
Psycharis, V. [4 ]
Raptopoulou, C. P. [4 ]
Hadjipavlou-Litina, D. [2 ]
Yiannaki, E. [5 ]
Dendrinou-Samara, C. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Gen & Inorgan Chem, Thessaloniki 54124, Greece
[2] Aristotle Univ Thessaloniki, Sch Pharm, Dept Pharmaceut Chem, Thessaloniki 54124, Greece
[3] Theagen Canc Hosp, Cell Culture Mol Modeling & Drug Design Lab, Symeonid Res Ctr, Thessaloniki, Greece
[4] NCSR Demokritos, Inst Nanosci & Nanotechnol, Aghia Paraskevi 15310, Attikis, Greece
[5] Theagen Canc Hosp, Hematol Lab, Thessaloniki, Greece
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 76卷
关键词
X-RAY-STRUCTURE; CONFORMER GENERATION; MIXED-LIGANDS; IN-VITRO; ACID; CANCER; LIPOXYGENASE; APOPTOSIS; 1,10-PHENANTHROLINE; 5-LIPOXYGENASE;
D O I
10.1016/j.msec.2017.03.157
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Seeking for copper based metallo-therapeutics, three triple bridged dinuclear copper(II) complexes [Cu-2(mu(2)-L-2)(bipy)(2)(mu(2)-OH)(mu(2)-H2O)](NO3)(2).H2O (1.H2O), [Cu-2(mu(2)-L-2)(biPY)(2)(mu(2)-OH)(mu(2)-NO3)I(NO3).0.6 MeOH.0.4H(2)O (2.0.6MeOH.0.4H(2)O) and [Cu-2(mu(2)-L-1)(biPY)(2)(mu(2)-OH)(mu(2)-NO3)(H2O)](NO3).2H(2)O (3.2H(2)O) where L-2 = 2-thiophene acetato, L-1 = 2-thiophene carboxylato and bipy = 2,2'-bipyridine were synthesized and structurally characterized. The complexes were subjected in vitro to a pharmacochemical evaluation for their antioxidant/anti-inflammatory activity, cytotoxicity and efficacy against human ovarian, lung, colon, breast, kidney and cervical cancer cell lines along with non tumor human lung and breast cell lines. The biological results support the structure related cytotoxic activity of the compounds. Complex 3 presented a combination of best anticancer and anti-inflammatory activities. A computational analysis over the LOX-3 protein structure 1JNQ was performed to support the possible mode of action. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1026 / 1040
页数:15
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