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

dc.contributor.authorMatos, Cristina P.
dc.contributor.authorAdiguzel, Zelal
dc.contributor.authorYildizhan, Yasemin
dc.contributor.authorCevatemre, Buse
dc.contributor.authorBagci-Onder, Tugba
dc.contributor.authorCevik, Ozge
dc.contributor.authorNunes, Patrique
dc.contributor.authorFerreira, Liliana P.
dc.contributor.authorCarvalho, Maria Deus
dc.contributor.authorCampos, Débora L. [UNESP]
dc.contributor.authorPavan, Fernando R. [UNESP]
dc.contributor.authorPessoa, João Costa
dc.contributor.authorGarcia, Maria Helena
dc.contributor.authorTomaz, Ana Isabel
dc.contributor.authorCorreia, Isabel
dc.contributor.authorAcilan, Ceyda
dc.contributor.institutionUniversidade de Lisboa
dc.contributor.institutionGenetic Engineering and Biotechnology Institute
dc.contributor.institutionKoc University Research Center for Translational Medicine (KUTTAM)
dc.contributor.institutionMedical School
dc.contributor.institutionSchool of Medicine
dc.contributor.institutionUniversity of Coimbra
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionCampo Grande
dc.date.accessioned2020-12-12T02:25:45Z
dc.date.available2020-12-12T02:25:45Z
dc.date.issued2019-12-01
dc.description.abstractThis 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 L2−, H2L = N,N-bis(2-hydroxy-3,5-dimethylbenzyl)-N-(2-pyridylmethyl)amine, and different aromatic bases (NN = 2,2′-bipyridine [Fe(L)(bipy)]PF6 (1), 1,10-phenanthroline [Fe(L)(phen)]PF6 (2), or a phenanthroline derivative co-ligand: [Fe(L)(amphen)]NO3 (3), [Fe(L)(amphen)]PF6 (3a), [Fe(L)(Clphen)]PF6 (4), [Fe(L)(epoxyphen)]PF6 (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)]NO3 (6), [Fe(phen)Cl3] (7) and [Fe(amphen)Cl3] (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.en
dc.description.affiliationCentro de Química Estrutural Instituto Superior Técnico Departamento de Engenharia Quimica Universidade de Lisboa, Av. Rovisco Pais 1
dc.description.affiliationTUBITAK Marmara Research Center Genetic Engineering and Biotechnology Institute
dc.description.affiliationKoc University Research Center for Translational Medicine (KUTTAM)
dc.description.affiliationKoc University Medical School
dc.description.affiliationAdnan Menderes University School of Medicine
dc.description.affiliationBioISI Faculdade de Ciências Universidade de Lisboa
dc.description.affiliationDepartment of Physics University of Coimbra
dc.description.affiliationCentro de Química e Bioquímica Faculdade de Ciências Universidade de Lisboa
dc.description.affiliationFaculdade de Ciências Farmacêuticas UNESP C.P.582
dc.description.affiliationCentro de Química Estrutural Faculdade de Ciencias Universidade de Lisboa Campo Grande
dc.description.affiliationUnespFaculdade de Ciências Farmacêuticas UNESP C.P.582
dc.description.sponsorshipFundação para a Ciência e a Tecnologia
dc.description.sponsorshipUniversidade de Lisboa
dc.description.sponsorshipFaculdade de Medicina da Universidade de São Paulo
dc.description.sponsorshipTürkiye Cumhuriyeti Disisleri Bakanligi
dc.description.sponsorshipIdFundação para a Ciência e a Tecnologia: IF/01179/2013
dc.description.sponsorshipIdUniversidade de Lisboa: LISBOA-01-0145-FEDER-007317
dc.description.sponsorshipIdFundação para a Ciência e a Tecnologia: RECI/QEQ-MED/0330/2012
dc.description.sponsorshipIdFundação para a Ciência e a Tecnologia: RECI/QEQ-QIN/0189/2012
dc.description.sponsorshipIdFundação para a Ciência e a Tecnologia: UID/BIO/04565/2013
dc.description.sponsorshipIdFundação para a Ciência e a Tecnologia: UID/MULTI/04349/2013
dc.description.sponsorshipIdFundação para a Ciência e a Tecnologia: UID/QUI/00100/2013
dc.identifierhttp://dx.doi.org/10.1016/j.dib.2019.104548
dc.identifier.citationData in Brief, v. 27.
dc.identifier.doi10.1016/j.dib.2019.104548
dc.identifier.issn2352-3409
dc.identifier.scopus2-s2.0-85066015347
dc.identifier.urihttp://hdl.handle.net/11449/201167
dc.language.isoeng
dc.relation.ispartofData in Brief
dc.sourceScopus
dc.subjectAnticancer
dc.subjectCytotoxicity
dc.subjectFe(III) complexes
dc.subjectGenotoxicity
dc.subjectPhenanthroline
dc.titleExperimental data on novel Fe(III)-complexes containing phenanthroline derivatives for their anticancer propertiesen
dc.typeData paper
unesp.author.orcid0000-0001-7096-4284[15]
unesp.departmentCiências Biológicas - FCFpt

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