DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline

Detalhes bibliográficos
Autor(a) principal: Almeida, Janaina do Couto
Data de Publicação: 2021
Outros Autores: Silva, Raphael T. C., Zanetti, Renan D. [UNESP], Moreira, Mariete B. [UNESP], Portes, Marcelo C., Polloni, Lorena, Vasconcelos Azevedo, Fernanda V. P. de, Von Poelhsitz, Gustavo, Pivatto, Marcos, Netto, Adelino V. G. [UNESP], Avila, Veridiana de Melo R., Manieri, Karyn F. [UNESP], Pavan, Fernando R. [UNESP], Da Costa Ferreira, Ana M., Guerra, Wendell
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.molstruc.2021.130234
http://hdl.handle.net/11449/210750
Resumo: Herein, we describe the synthesis and characterization of novel heteroleptic copper(II) complexes, [Cu(2-HNA)(phen)ClO4]center dot 1 center dot 5H(2)O I, [Cu(6-HNA)(phen)ClO4]center dot H2O II, [Cu(QNA)(phen)ClO4]center dot 0 center dot 5H(2)O III and [Cu(2-MNA)(phen)ClO4]center dot 0 center dot 5H(2)O IV, where 2-HNA = 2-hydroxynicotinic acid, 6-HNA = 6-hydroxynicotinic acid, QNA = 2-quinolinecarboxylic acid, 2-MNA = 2-mercaptonicotinic acid and phen = 1,10-phenanthroline. The spectral data indicate a square-pyramidal geometry around the copper(II) ion in the solid state, with an acid derivative and 1,10-phenanthroline (N-N) acting as bidentate ligands. A perchlorate ion in the apical position completes the metal coordination sphere. All these complexes exhibited potent activity against the Mycobacterium tuberculosis H37Rv strain, with MIC values in the range of few mu M. The cytotoxic activity of these compounds was also investigated toward tumor cell lines (MDA-MB-231 and MCF-7) and in a non-tumorigenic cell line (MCF-10A). Complex I was the most active (IC50 = 4.2 mu M) and selective (SI > 3) toward MDA-MB-231 cells. DNA binding studies performed by circular dichroism (CD) and UV-Vis spectroscopic methods, using a Hoechst 33258 displacement assay, indicated that these complexes can efficiently bind to ct-DNA, with K-b values in the range of 10(3) M-1. (c) 2021 Elsevier B.V. All rights reserved.
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spelling DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthrolineCopper(II) complexesCytotoxic activityMycobacterium tuberculosisDNA binding studiesS[ectroscopic methodsHerein, we describe the synthesis and characterization of novel heteroleptic copper(II) complexes, [Cu(2-HNA)(phen)ClO4]center dot 1 center dot 5H(2)O I, [Cu(6-HNA)(phen)ClO4]center dot H2O II, [Cu(QNA)(phen)ClO4]center dot 0 center dot 5H(2)O III and [Cu(2-MNA)(phen)ClO4]center dot 0 center dot 5H(2)O IV, where 2-HNA = 2-hydroxynicotinic acid, 6-HNA = 6-hydroxynicotinic acid, QNA = 2-quinolinecarboxylic acid, 2-MNA = 2-mercaptonicotinic acid and phen = 1,10-phenanthroline. The spectral data indicate a square-pyramidal geometry around the copper(II) ion in the solid state, with an acid derivative and 1,10-phenanthroline (N-N) acting as bidentate ligands. A perchlorate ion in the apical position completes the metal coordination sphere. All these complexes exhibited potent activity against the Mycobacterium tuberculosis H37Rv strain, with MIC values in the range of few mu M. The cytotoxic activity of these compounds was also investigated toward tumor cell lines (MDA-MB-231 and MCF-7) and in a non-tumorigenic cell line (MCF-10A). Complex I was the most active (IC50 = 4.2 mu M) and selective (SI > 3) toward MDA-MB-231 cells. DNA binding studies performed by circular dichroism (CD) and UV-Vis spectroscopic methods, using a Hoechst 33258 displacement assay, indicated that these complexes can efficiently bind to ct-DNA, with K-b values in the range of 10(3) M-1. (c) 2021 Elsevier B.V. All rights reserved.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)Univ Fed Uberlandia, Inst Quim, Av Joao Naves de Avila 2121,Campus Santa Monica, BR-38400902 Uberlandia, MG, BrazilUniv Estadual Paulista, Inst Quim, Araraquara, SP, BrazilUniv Estadual Londrina, Dept Quim, Londrina, Parana, BrazilUniv Sao Paulo, Dept Quim Fundamental, Inst Quim, Sao Paulo, SP, BrazilUniv Fed Uberlandia, Inst Biotecnol, Uberlandia, MG, BrazilUniv Estadual Paulista, Fac Ciencias Farmaceut, Campus Araraquara, Araraquara, SP, BrazilUniv Estadual Paulista, Inst Quim, Araraquara, SP, BrazilUniv Estadual Paulista, Fac Ciencias Farmaceut, Campus Araraquara, Araraquara, SP, BrazilCNPq: 304316/2018-0FAPEMIG: APQ-00330-14Elsevier B.V.Universidade Federal de Uberlândia (UFU)Universidade Estadual Paulista (Unesp)Universidade Estadual de Londrina (UEL)Universidade de São Paulo (USP)Almeida, Janaina do CoutoSilva, Raphael T. C.Zanetti, Renan D. [UNESP]Moreira, Mariete B. [UNESP]Portes, Marcelo C.Polloni, LorenaVasconcelos Azevedo, Fernanda V. P. deVon Poelhsitz, GustavoPivatto, MarcosNetto, Adelino V. G. [UNESP]Avila, Veridiana de Melo R.Manieri, Karyn F. [UNESP]Pavan, Fernando R. [UNESP]Da Costa Ferreira, Ana M.Guerra, Wendell2021-06-26T05:25:32Z2021-06-26T05:25:32Z2021-07-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article9http://dx.doi.org/10.1016/j.molstruc.2021.130234Journal Of Molecular Structure. Amsterdam: Elsevier, v. 1235, 9 p., 2021.0022-2860http://hdl.handle.net/11449/21075010.1016/j.molstruc.2021.130234WOS:000640573700011Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Molecular Structureinfo:eu-repo/semantics/openAccess2024-06-24T13:08:35Zoai:repositorio.unesp.br:11449/210750Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:45:01.126642Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
title DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
spellingShingle DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
Almeida, Janaina do Couto
Copper(II) complexes
Cytotoxic activity
Mycobacterium tuberculosis
DNA binding studies
S[ectroscopic methods
title_short DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
title_full DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
title_fullStr DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
title_full_unstemmed DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
title_sort DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
author Almeida, Janaina do Couto
author_facet Almeida, Janaina do Couto
Silva, Raphael T. C.
Zanetti, Renan D. [UNESP]
Moreira, Mariete B. [UNESP]
Portes, Marcelo C.
Polloni, Lorena
Vasconcelos Azevedo, Fernanda V. P. de
Von Poelhsitz, Gustavo
Pivatto, Marcos
Netto, Adelino V. G. [UNESP]
Avila, Veridiana de Melo R.
Manieri, Karyn F. [UNESP]
Pavan, Fernando R. [UNESP]
Da Costa Ferreira, Ana M.
Guerra, Wendell
author_role author
author2 Silva, Raphael T. C.
Zanetti, Renan D. [UNESP]
Moreira, Mariete B. [UNESP]
Portes, Marcelo C.
Polloni, Lorena
Vasconcelos Azevedo, Fernanda V. P. de
Von Poelhsitz, Gustavo
Pivatto, Marcos
Netto, Adelino V. G. [UNESP]
Avila, Veridiana de Melo R.
Manieri, Karyn F. [UNESP]
Pavan, Fernando R. [UNESP]
Da Costa Ferreira, Ana M.
Guerra, Wendell
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Uberlândia (UFU)
Universidade Estadual Paulista (Unesp)
Universidade Estadual de Londrina (UEL)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Almeida, Janaina do Couto
Silva, Raphael T. C.
Zanetti, Renan D. [UNESP]
Moreira, Mariete B. [UNESP]
Portes, Marcelo C.
Polloni, Lorena
Vasconcelos Azevedo, Fernanda V. P. de
Von Poelhsitz, Gustavo
Pivatto, Marcos
Netto, Adelino V. G. [UNESP]
Avila, Veridiana de Melo R.
Manieri, Karyn F. [UNESP]
Pavan, Fernando R. [UNESP]
Da Costa Ferreira, Ana M.
Guerra, Wendell
dc.subject.por.fl_str_mv Copper(II) complexes
Cytotoxic activity
Mycobacterium tuberculosis
DNA binding studies
S[ectroscopic methods
topic Copper(II) complexes
Cytotoxic activity
Mycobacterium tuberculosis
DNA binding studies
S[ectroscopic methods
description Herein, we describe the synthesis and characterization of novel heteroleptic copper(II) complexes, [Cu(2-HNA)(phen)ClO4]center dot 1 center dot 5H(2)O I, [Cu(6-HNA)(phen)ClO4]center dot H2O II, [Cu(QNA)(phen)ClO4]center dot 0 center dot 5H(2)O III and [Cu(2-MNA)(phen)ClO4]center dot 0 center dot 5H(2)O IV, where 2-HNA = 2-hydroxynicotinic acid, 6-HNA = 6-hydroxynicotinic acid, QNA = 2-quinolinecarboxylic acid, 2-MNA = 2-mercaptonicotinic acid and phen = 1,10-phenanthroline. The spectral data indicate a square-pyramidal geometry around the copper(II) ion in the solid state, with an acid derivative and 1,10-phenanthroline (N-N) acting as bidentate ligands. A perchlorate ion in the apical position completes the metal coordination sphere. All these complexes exhibited potent activity against the Mycobacterium tuberculosis H37Rv strain, with MIC values in the range of few mu M. The cytotoxic activity of these compounds was also investigated toward tumor cell lines (MDA-MB-231 and MCF-7) and in a non-tumorigenic cell line (MCF-10A). Complex I was the most active (IC50 = 4.2 mu M) and selective (SI > 3) toward MDA-MB-231 cells. DNA binding studies performed by circular dichroism (CD) and UV-Vis spectroscopic methods, using a Hoechst 33258 displacement assay, indicated that these complexes can efficiently bind to ct-DNA, with K-b values in the range of 10(3) M-1. (c) 2021 Elsevier B.V. All rights reserved.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-26T05:25:32Z
2021-06-26T05:25:32Z
2021-07-05
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.molstruc.2021.130234
Journal Of Molecular Structure. Amsterdam: Elsevier, v. 1235, 9 p., 2021.
0022-2860
http://hdl.handle.net/11449/210750
10.1016/j.molstruc.2021.130234
WOS:000640573700011
url http://dx.doi.org/10.1016/j.molstruc.2021.130234
http://hdl.handle.net/11449/210750
identifier_str_mv Journal Of Molecular Structure. Amsterdam: Elsevier, v. 1235, 9 p., 2021.
0022-2860
10.1016/j.molstruc.2021.130234
WOS:000640573700011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of Molecular Structure
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 9
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
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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