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Synthesis, characterization and biological activities of semicarbazones and their copper complexes.
Venkatachalam, Taracad K; Bernhardt, Paul V; Noble, Chris J; Fletcher, Nicholas; Pierens, Gregory K; Thurecht, Kris J; Reutens, David C.
Afiliación
  • Venkatachalam TK; Centre for Advanced Imaging, School of Chemistry University of Queensland, St. Lucia, Brisbane 4072, Australia. Electronic address: t.venkatachalam@uq.edu.au.
  • Bernhardt PV; Centre for Advanced Imaging, School of Chemistry University of Queensland, St. Lucia, Brisbane 4072, Australia.
  • Noble CJ; Centre for Advanced Imaging, School of Chemistry University of Queensland, St. Lucia, Brisbane 4072, Australia.
  • Fletcher N; Centre for Advanced Imaging, School of Chemistry University of Queensland, St. Lucia, Brisbane 4072, Australia.
  • Pierens GK; Centre for Advanced Imaging, School of Chemistry University of Queensland, St. Lucia, Brisbane 4072, Australia.
  • Thurecht KJ; Centre for Advanced Imaging, School of Chemistry University of Queensland, St. Lucia, Brisbane 4072, Australia.
  • Reutens DC; Centre for Advanced Imaging, School of Chemistry University of Queensland, St. Lucia, Brisbane 4072, Australia.
J Inorg Biochem ; 162: 295-308, 2016 09.
Article en En | MEDLINE | ID: mdl-27138101
ABSTRACT
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Semicarbazonas / Tiosemicarbazonas / Cobre / Complejos de Coordinación / Antineoplásicos Límite: Humans Idioma: En Revista: J Inorg Biochem Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Semicarbazonas / Tiosemicarbazonas / Cobre / Complejos de Coordinación / Antineoplásicos Límite: Humans Idioma: En Revista: J Inorg Biochem Año: 2016 Tipo del documento: Article