DNA interactions, antitubercular and cytotoxic activity of heteroleptic Cu-II complexes containing 1,10-phenanthroline
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , , , , |
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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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 |
|
_version_ |
1808129548127043584 |