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Experimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer properties

This dataset is related to the research article entitled “May iron(III) complexes containing phenanthroline derivatives as ligands be prospective anticancer agents?” [1]. It includes the characterization by UV–Vis absorption spectroscopy and magnetic techniques of a group of mixed ligand Fe(III) com...

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Autores principales: Matos, Cristina P., Adiguzel, Zelal, Yildizhan, Yasemin, Cevatemre, Buse, Bagci-Onder, Tugba, Cevik, Ozge, Nunes, Patrique, Ferreira, Liliana P., Carvalho, Maria Deus, Campos, Débora L., Pavan, Fernando R., Pessoa, João Costa, Garcia, Maria Helena, Tomaz, Ana Isabel, Correia, Isabel, Acilan, Ceyda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817691/
https://www.ncbi.nlm.nih.gov/pubmed/31681825
http://dx.doi.org/10.1016/j.dib.2019.104548
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author Matos, Cristina P.
Adiguzel, Zelal
Yildizhan, Yasemin
Cevatemre, Buse
Bagci-Onder, Tugba
Cevik, Ozge
Nunes, Patrique
Ferreira, Liliana P.
Carvalho, Maria Deus
Campos, Débora L.
Pavan, Fernando R.
Pessoa, João Costa
Garcia, Maria Helena
Tomaz, Ana Isabel
Correia, Isabel
Acilan, Ceyda
author_facet Matos, Cristina P.
Adiguzel, Zelal
Yildizhan, Yasemin
Cevatemre, Buse
Bagci-Onder, Tugba
Cevik, Ozge
Nunes, Patrique
Ferreira, Liliana P.
Carvalho, Maria Deus
Campos, Débora L.
Pavan, Fernando R.
Pessoa, João Costa
Garcia, Maria Helena
Tomaz, Ana Isabel
Correia, Isabel
Acilan, Ceyda
author_sort Matos, Cristina P.
collection PubMed
description This dataset is related to the research article entitled “May iron(III) complexes containing phenanthroline derivatives as ligands be prospective anticancer agents?” [1]. It includes the characterization by UV–Vis absorption spectroscopy and magnetic techniques of a group of mixed ligand Fe(III) complexes bearing a tripodal aminophenolate ligand L(2−), H(2)L = N,N-bis(2-hydroxy-3,5-dimethylbenzyl)-N-(2-pyridylmethyl)amine, and different aromatic bases (NN = 2,2′-bipyridine [Fe(L)(bipy)]PF(6) (1), 1,10-phenanthroline [Fe(L)(phen)]PF(6) (2), or a phenanthroline derivative co-ligand: [Fe(L)(amphen)]NO(3) (3), [Fe(L)(amphen)]PF(6) (3a), [Fe(L)(Clphen)]PF(6) (4), [Fe(L)(epoxyphen)]PF(6) (5) (where amphen = 1,10-phenanthroline-5-amine, epoxyphen = 5,6-epoxy-5,6-dihydro-1,10-phenanthroline, Clphen = 5-chloro-1,10-phenanthroline), as well as [Fe(L)(EtOH)]NO(3) (6), [Fe(phen)Cl(3)] (7) and [Fe(amphen)Cl(3)] (8). Data on their hydrolytic stability in physiological buffers is shown, as well as on their interaction with calf thymus DNA by spectroscopic tools. Additionally, the anticancer efficacy and the cellular death mechanisms activated in response to these drugs in HeLa, H1299 and MDA-MB-231 cells are provided.
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spelling pubmed-68176912019-11-01 Experimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer properties Matos, Cristina P. Adiguzel, Zelal Yildizhan, Yasemin Cevatemre, Buse Bagci-Onder, Tugba Cevik, Ozge Nunes, Patrique Ferreira, Liliana P. Carvalho, Maria Deus Campos, Débora L. Pavan, Fernando R. Pessoa, João Costa Garcia, Maria Helena Tomaz, Ana Isabel Correia, Isabel Acilan, Ceyda Data Brief Biochemistry, Genetics and Molecular Biology This dataset is related to the research article entitled “May iron(III) complexes containing phenanthroline derivatives as ligands be prospective anticancer agents?” [1]. It includes the characterization by UV–Vis absorption spectroscopy and magnetic techniques of a group of mixed ligand Fe(III) complexes bearing a tripodal aminophenolate ligand L(2−), H(2)L = N,N-bis(2-hydroxy-3,5-dimethylbenzyl)-N-(2-pyridylmethyl)amine, and different aromatic bases (NN = 2,2′-bipyridine [Fe(L)(bipy)]PF(6) (1), 1,10-phenanthroline [Fe(L)(phen)]PF(6) (2), or a phenanthroline derivative co-ligand: [Fe(L)(amphen)]NO(3) (3), [Fe(L)(amphen)]PF(6) (3a), [Fe(L)(Clphen)]PF(6) (4), [Fe(L)(epoxyphen)]PF(6) (5) (where amphen = 1,10-phenanthroline-5-amine, epoxyphen = 5,6-epoxy-5,6-dihydro-1,10-phenanthroline, Clphen = 5-chloro-1,10-phenanthroline), as well as [Fe(L)(EtOH)]NO(3) (6), [Fe(phen)Cl(3)] (7) and [Fe(amphen)Cl(3)] (8). Data on their hydrolytic stability in physiological buffers is shown, as well as on their interaction with calf thymus DNA by spectroscopic tools. Additionally, the anticancer efficacy and the cellular death mechanisms activated in response to these drugs in HeLa, H1299 and MDA-MB-231 cells are provided. Elsevier 2019-09-27 /pmc/articles/PMC6817691/ /pubmed/31681825 http://dx.doi.org/10.1016/j.dib.2019.104548 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Biochemistry, Genetics and Molecular Biology
Matos, Cristina P.
Adiguzel, Zelal
Yildizhan, Yasemin
Cevatemre, Buse
Bagci-Onder, Tugba
Cevik, Ozge
Nunes, Patrique
Ferreira, Liliana P.
Carvalho, Maria Deus
Campos, Débora L.
Pavan, Fernando R.
Pessoa, João Costa
Garcia, Maria Helena
Tomaz, Ana Isabel
Correia, Isabel
Acilan, Ceyda
Experimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer properties
title Experimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer properties
title_full Experimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer properties
title_fullStr Experimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer properties
title_full_unstemmed Experimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer properties
title_short Experimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer properties
title_sort experimental data on novel fe(iii)-complexes containing phenanthroline derivatives for their anticancer properties
topic Biochemistry, Genetics and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817691/
https://www.ncbi.nlm.nih.gov/pubmed/31681825
http://dx.doi.org/10.1016/j.dib.2019.104548
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