Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity

Detalhes bibliográficos
Autor(a) principal: Tarallo, M. Belen
Data de Publicação: 2008
Outros Autores: Urquiola, Carolina, Monge, Antonio, Pavan, Fernando R. [UNESP], Leite, Clarice Q. [UNESP], Torre, Maria H., Gambino, Dinorah, Collery, P., Maymard, I, Theophanides, T., Khassanova, L., Collery, T.
Tipo de documento: Artigo de conferência
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/197384
Resumo: Three new iron complexes with 3-aminoquinoxaline-2-carbonitrile N-1, N-4-dioxide derivatives (L) with stoichiometries [Fe(L1)(2)], [Fe(L1)(3)] and [Fe(L2)(3)]center dot 5H(2)O were synthesized and characterized. Both ligands and complexes showed in vitro activity against Mycobacterium. tuberculosis H(37)Rv (ATCC 27294) (MIC=3.9 mu g/mL for [Fe(L1)(2)] and [Fe(L2)(3)]center dot 5H(2)O and 7.8 mu g/mL for [Fe(L1)(3)]) with low citotoxicity. Two of the three complexes presented better activity than the free ligands, demonstrating that metal coordination can favorably modify the profile of antimycobacterial activity of 3-aminoquinoxaline-2-carbonitrile N-1,N-4-dioxide derivatives.
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spelling Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activityM. tuberculosisquinoxaline N-1,N-4-dioxidesiron complexesThree new iron complexes with 3-aminoquinoxaline-2-carbonitrile N-1, N-4-dioxide derivatives (L) with stoichiometries [Fe(L1)(2)], [Fe(L1)(3)] and [Fe(L2)(3)]center dot 5H(2)O were synthesized and characterized. Both ligands and complexes showed in vitro activity against Mycobacterium. tuberculosis H(37)Rv (ATCC 27294) (MIC=3.9 mu g/mL for [Fe(L1)(2)] and [Fe(L2)(3)]center dot 5H(2)O and 7.8 mu g/mL for [Fe(L1)(3)]) with low citotoxicity. Two of the three complexes presented better activity than the free ligands, demonstrating that metal coordination can favorably modify the profile of antimycobacterial activity of 3-aminoquinoxaline-2-carbonitrile N-1,N-4-dioxide derivatives.CHLCCPEDECIBA QuimicaUniv Republica, Fac Quim, Catedra Quim Inorgan, Gral Flores 2124,CC 1157, Montevideo 11800, UruguayUniv Navarra, CIFA, Pamplona, SpainUnesp, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, BrazilUnesp, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, BrazilJohn Libbey EurotextUniv RepublicaUniv NavarraUniversidade Estadual Paulista (Unesp)Tarallo, M. BelenUrquiola, CarolinaMonge, AntonioPavan, Fernando R. [UNESP]Leite, Clarice Q. [UNESP]Torre, Maria H.Gambino, DinorahCollery, P.Maymard, ITheophanides, T.Khassanova, L.Collery, T.2020-12-10T22:01:40Z2020-12-10T22:01:40Z2008-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObject867-+Metal Ions In Biology And Medicine, Vol 10. Montrouge: John Libbey Eurotext, v. 10, p. 867-+, 2008.1257-2535http://hdl.handle.net/11449/197384WOS:000258426900145Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMetal Ions In Biology And Medicine, Vol 10info:eu-repo/semantics/openAccess2021-10-23T11:43:35Zoai:repositorio.unesp.br:11449/197384Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T11:43:35Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity
title Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity
spellingShingle Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity
Tarallo, M. Belen
M. tuberculosis
quinoxaline N-1,N-4-dioxides
iron complexes
title_short Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity
title_full Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity
title_fullStr Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity
title_full_unstemmed Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity
title_sort Novel iron complexes with quinoxaline N-1,N-4-dioxide derivatives: synthesis, characterization and antimycobacterial activity
author Tarallo, M. Belen
author_facet Tarallo, M. Belen
Urquiola, Carolina
Monge, Antonio
Pavan, Fernando R. [UNESP]
Leite, Clarice Q. [UNESP]
Torre, Maria H.
Gambino, Dinorah
Collery, P.
Maymard, I
Theophanides, T.
Khassanova, L.
Collery, T.
author_role author
author2 Urquiola, Carolina
Monge, Antonio
Pavan, Fernando R. [UNESP]
Leite, Clarice Q. [UNESP]
Torre, Maria H.
Gambino, Dinorah
Collery, P.
Maymard, I
Theophanides, T.
Khassanova, L.
Collery, T.
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Univ Republica
Univ Navarra
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Tarallo, M. Belen
Urquiola, Carolina
Monge, Antonio
Pavan, Fernando R. [UNESP]
Leite, Clarice Q. [UNESP]
Torre, Maria H.
Gambino, Dinorah
Collery, P.
Maymard, I
Theophanides, T.
Khassanova, L.
Collery, T.
dc.subject.por.fl_str_mv M. tuberculosis
quinoxaline N-1,N-4-dioxides
iron complexes
topic M. tuberculosis
quinoxaline N-1,N-4-dioxides
iron complexes
description Three new iron complexes with 3-aminoquinoxaline-2-carbonitrile N-1, N-4-dioxide derivatives (L) with stoichiometries [Fe(L1)(2)], [Fe(L1)(3)] and [Fe(L2)(3)]center dot 5H(2)O were synthesized and characterized. Both ligands and complexes showed in vitro activity against Mycobacterium. tuberculosis H(37)Rv (ATCC 27294) (MIC=3.9 mu g/mL for [Fe(L1)(2)] and [Fe(L2)(3)]center dot 5H(2)O and 7.8 mu g/mL for [Fe(L1)(3)]) with low citotoxicity. Two of the three complexes presented better activity than the free ligands, demonstrating that metal coordination can favorably modify the profile of antimycobacterial activity of 3-aminoquinoxaline-2-carbonitrile N-1,N-4-dioxide derivatives.
publishDate 2008
dc.date.none.fl_str_mv 2008-01-01
2020-12-10T22:01:40Z
2020-12-10T22:01:40Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/conferenceObject
format conferenceObject
status_str publishedVersion
dc.identifier.uri.fl_str_mv Metal Ions In Biology And Medicine, Vol 10. Montrouge: John Libbey Eurotext, v. 10, p. 867-+, 2008.
1257-2535
http://hdl.handle.net/11449/197384
WOS:000258426900145
identifier_str_mv Metal Ions In Biology And Medicine, Vol 10. Montrouge: John Libbey Eurotext, v. 10, p. 867-+, 2008.
1257-2535
WOS:000258426900145
url http://hdl.handle.net/11449/197384
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Metal Ions In Biology And Medicine, Vol 10
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 867-+
dc.publisher.none.fl_str_mv John Libbey Eurotext
publisher.none.fl_str_mv John Libbey Eurotext
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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