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Design and synthesis of thalidomide based dithiocarbamate Cu(II), Ni(II) and Ru(III) complexes as anticancer agents
被引:119
|作者:
Ali, Imran
[1
]
Wani, Waseem A.
[1
]
Saleem, Kishwar
[1
]
Hseih, Ming-Fa
[2
]
机构:
[1] Jamia Millia Islamia, Dept Chem, New Delhi 110025, India
[2] Chung Yuan Christian Univ, Dept Biomed Engn, Chungli, Taiwan
来源:
关键词:
Dithiocarbamate ligand;
Metal complexes;
DNA binding;
Modeling;
Hemolysis assays;
Anticancer profiles;
DNA-BINDING;
ANTITUMOR-ACTIVITY;
CRYSTAL-STRUCTURE;
ACID;
COPPER(II);
CLEAVAGE;
CANCER;
HYDROLYSIS;
REACTIVITY;
LIGAND;
D O I:
10.1016/j.poly.2013.03.056
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
In view of the growing interest in the design of metal complexes as anticancer drugs, a thalidomide based dithiocarbamate ligand; 3-(1,3-dioxoisoindolin-2-yl)-2,6-dioxopiperidine-1 -carbodithioate was synthesized by the sodium hydroxide assisted reaction of thalidomide with carbon disulfide at 0-5 degrees C. Metal complexes of the ligand with copper(II), nickel(II) and ruthenium(III) ions were also prepared. The synthesized ligand and its complexes were purified and characterized by various chromatographic and spectroscopic techniques. Robust nature of the complexes in 5% DMSO solutions of PBS at 7.4 pH was revealed from their solution stability studies. DNA binding constants (K-b) for ligand, copper, nickel and ruthenium complexes were 3.6 x 10(4), 1.4 x 10(5), 3.8 x 10(4) and 4.5 x 10(4) M-1, indicating strong binding with DNA. In silico studies indicated that the ligand preferred to enter into the minor groove of DNA forming one H bond between the oxygen atom of carbonyl group of the pyrrolidinedione moiety and hydrogen atom of adenine. Hemolysis assays revealed that ligand and its complexes were less toxic to RBCs as compared to doxorubicin. All the compounds showed moderate anticancer activities on MCF-7 (wild type) cancer cell lines. The reported molecules may be treated as potential future anticancer candidates. (C) 2013 Elsevier Ltd. All rights reserved.
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页码:134 / 143
页数:10
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