Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014001000010 |
Resumo: | CoIII complexes derived from 2-acetylpyridine N(4)-R thiosemicarbazone (Hatc-R, R = alkyl, aryl) have been characterized by elemental analysis, FTIR, UV-Visible and ¹H NMR spectroscopies, cyclic voltammetry (CV), conductimetry measurements and single crystal X-ray diffractometry. The results obtained are consistent with the oxidation of the CoII center to CoIII upon coordination of the monoanionic N,N,S-tridentate thiosemicarbazone ligands, resulting in octahedral ionic complexes of the type [Co(atc-R)2]Cl. Electrochemistry studies show two reversible processes referring to the redox couples CoIII/CoII and CoII/CoI which can be modified by the inductive effects of the substituents groups at the N4 position of the ligands. Two CoIII complexes showed satisfactory activity with minimal inhibitory concentration value under 10 µmol L- 1 and one presented quite low cytotoxicity against VERO and J774A.1 cells (IC50), resulting in high selectivity index (SI > 10). |
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Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agentscobalt(III)thiosemicarbazonesanti-mycobacterium tuberculosis activityCoIII complexes derived from 2-acetylpyridine N(4)-R thiosemicarbazone (Hatc-R, R = alkyl, aryl) have been characterized by elemental analysis, FTIR, UV-Visible and ¹H NMR spectroscopies, cyclic voltammetry (CV), conductimetry measurements and single crystal X-ray diffractometry. The results obtained are consistent with the oxidation of the CoII center to CoIII upon coordination of the monoanionic N,N,S-tridentate thiosemicarbazone ligands, resulting in octahedral ionic complexes of the type [Co(atc-R)2]Cl. Electrochemistry studies show two reversible processes referring to the redox couples CoIII/CoII and CoII/CoI which can be modified by the inductive effects of the substituents groups at the N4 position of the ligands. Two CoIII complexes showed satisfactory activity with minimal inhibitory concentration value under 10 µmol L- 1 and one presented quite low cytotoxicity against VERO and J774A.1 cells (IC50), resulting in high selectivity index (SI > 10).Sociedade Brasileira de Química2014-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014001000010Journal of the Brazilian Chemical Society v.25 n.10 2014reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20140149info:eu-repo/semantics/openAccessOliveira,Carolina G.Maia,Pedro Ivo da S.Miyata,MarceloPavan,Fernando R.Leite,Clarice Q. F.Almeida,Eduardo Tonon deDeflon,Victor M.eng2014-10-27T00:00:00Zoai:scielo:S0103-50532014001000010Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2014-10-27T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents |
title |
Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents |
spellingShingle |
Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents Oliveira,Carolina G. cobalt(III) thiosemicarbazones anti-mycobacterium tuberculosis activity |
title_short |
Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents |
title_full |
Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents |
title_fullStr |
Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents |
title_full_unstemmed |
Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents |
title_sort |
Cobalt(III) complexes with thiosemicarbazones as potential anti-Mycobacterium tuberculosis agents |
author |
Oliveira,Carolina G. |
author_facet |
Oliveira,Carolina G. Maia,Pedro Ivo da S. Miyata,Marcelo Pavan,Fernando R. Leite,Clarice Q. F. Almeida,Eduardo Tonon de Deflon,Victor M. |
author_role |
author |
author2 |
Maia,Pedro Ivo da S. Miyata,Marcelo Pavan,Fernando R. Leite,Clarice Q. F. Almeida,Eduardo Tonon de Deflon,Victor M. |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Oliveira,Carolina G. Maia,Pedro Ivo da S. Miyata,Marcelo Pavan,Fernando R. Leite,Clarice Q. F. Almeida,Eduardo Tonon de Deflon,Victor M. |
dc.subject.por.fl_str_mv |
cobalt(III) thiosemicarbazones anti-mycobacterium tuberculosis activity |
topic |
cobalt(III) thiosemicarbazones anti-mycobacterium tuberculosis activity |
description |
CoIII complexes derived from 2-acetylpyridine N(4)-R thiosemicarbazone (Hatc-R, R = alkyl, aryl) have been characterized by elemental analysis, FTIR, UV-Visible and ¹H NMR spectroscopies, cyclic voltammetry (CV), conductimetry measurements and single crystal X-ray diffractometry. The results obtained are consistent with the oxidation of the CoII center to CoIII upon coordination of the monoanionic N,N,S-tridentate thiosemicarbazone ligands, resulting in octahedral ionic complexes of the type [Co(atc-R)2]Cl. Electrochemistry studies show two reversible processes referring to the redox couples CoIII/CoII and CoII/CoI which can be modified by the inductive effects of the substituents groups at the N4 position of the ligands. Two CoIII complexes showed satisfactory activity with minimal inhibitory concentration value under 10 µmol L- 1 and one presented quite low cytotoxicity against VERO and J774A.1 cells (IC50), resulting in high selectivity index (SI > 10). |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-10-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014001000010 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014001000010 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/0103-5053.20140149 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.25 n.10 2014 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
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SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
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1750318176524042240 |