Synthesis, characterization and biological activities of semicarbazones and their copper complexes

被引:26
|
作者
Venkatachalam, Taracad K. [1 ]
Bernhardt, Paul V. [1 ]
Noble, Chris J. [1 ]
Fletcher, Nicholas [1 ]
Pierens, Gregory K. [1 ]
Thurecht, Kris J. [1 ]
Reutens, David C. [1 ]
机构
[1] Univ Queensland, Ctr Adv Imaging, Sch Chem, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
Synthesis; Characterization; Semicarbazones; Copper complex; X-ray crystallography; Biological activity; THIOSEMICARBAZONES; IRON;
D O I
10.1016/j.jinorgbio.2016.04.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Substituted semicarbazones/thiosemicarbazones and their copper complexes have been prepared and several single crystal structures examined. The copper complexes of these semicarbazone/thiosemicarbazones were prepared and several crystal structures examined. The single crystal X-ray structure of the pyridyl-substituted semicarbazone showed two types of copper complexes, a monomer and a dimer. We also found that the p-nitrophenyl semicarbazone formed a conventional 'magic lantern' acetate-bridged dimer. Electron Paramagnetic Resonance (EPR) of several of the copper complexes was consistent with the results of single crystal X-ray crystallography. The EPR spectra of the p-nitrophenyl semicarbazone copper complex in dimethylsulfoxide (DMSO) showed the presence of two species, confirming the structural information. Since thiosemicarbazones and semicarbazones have been reported to exhibit anticancer activity, we examined the anticancer activity of several of the derivatives reported in the present study and interestingly only the thiosemicarbazone showed activity while the semicarbazones were not active indicating that introduction of sulphur atom alters the biological profile of these thiosemicarbazones. (C) 2016 Elsevier Inc All rights reserved.
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页码:295 / 308
页数:14
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