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http://hdl.handle.net/1843/56376
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DC Field | Value | Language |
---|---|---|
dc.creator | Aline Farias Moreira da Silva | pt_BR |
dc.creator | Carlos Basílio Pinheiro | pt_BR |
dc.creator | Jackson Antonio Lamounier Camargos Resende | pt_BR |
dc.creator | Mauricio Lanznaster | pt_BR |
dc.date.accessioned | 2023-07-17T13:22:12Z | - |
dc.date.available | 2023-07-17T13:22:12Z | - |
dc.date.issued | 2017 | - |
dc.citation.volume | 123 | pt_BR |
dc.citation.spage | 132 | pt_BR |
dc.citation.epage | 137 | pt_BR |
dc.identifier.doi | https://doi.org/10.1016/j.poly.2016.10.042 | pt_BR |
dc.identifier.issn | 1873-3719 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/1843/56376 | - |
dc.description.resumo | Two new iron(III) complexes, [Fe(bhnq)(L1)]NO3·CH3OH·2H2O (1) and [Fe(bhnq)(L2)]ClO4·CH3OH (2) (L1 = N,N′-bis(pyridin-2-ylmethyl)ethylenediamine and L2 = N,N′-dimethyl-N,N′-bis(pyridin-2-ylmethyl)ethylenediamine), were investigated as potential candidates for bioreductively activated prodrugs. These complexes present a distorted octahedral structure with 2,2′-bis(3-hydroxy-1,4-naphthoquinone), (bhnq)2−, coordinated in a bidentate fashion to the iron(III) ion. A reversible wave associated with the Fe3+/Fe2+couple was observed in MeCN for 1 and 2 respectively at −0.05 V and 0.01 V versus SHE. Unlike previously studied cobalt(III)-based analogs and one iron(III) platform that showed efficient bioreductive activation, complexes 1 and 2 undergo fast dissociation in aqueous buffered solutions with immediate release of the bhnq2− ligand. Therefore, we conclude that the labile 3d5 iron(III) ion is a limited bioreducible carrier for naphthoquinone-based prodrugs when coordinated to this [N2NPy2] platform. Considerable modification of the current ligands or the meticulous selection of other alternative ligand platforms may be necessary to attain this goal. | pt_BR |
dc.description.sponsorship | CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico | pt_BR |
dc.description.sponsorship | FAPERJ - Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro | pt_BR |
dc.language | eng | pt_BR |
dc.publisher | Universidade Federal de Minas Gerais | pt_BR |
dc.publisher.country | Brasil | pt_BR |
dc.publisher.department | ICX - DEPARTAMENTO DE FÍSICA | pt_BR |
dc.publisher.initials | UFMG | pt_BR |
dc.relation.ispartof | Polyhedron | - |
dc.rights | Acesso Restrito | pt_BR |
dc.subject | Bioreductively activated prodrugs | pt_BR |
dc.subject | Prodrugs activated by hypoxia | pt_BR |
dc.subject | Bioreducible carrier | pt_BR |
dc.subject | Iron | pt_BR |
dc.subject.other | Ferro | pt_BR |
dc.subject.other | Anoxemia | pt_BR |
dc.title | Evaluation of Iron(iii)-N(amine)2N(py)2 complexes as potential bioreductively activated carriers for naphthoquinone-based drugs | pt_BR |
dc.type | Artigo de Periódico | pt_BR |
dc.url.externa | https://www.sciencedirect.com/science/article/pii/S0277538716305393 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0001-6550-1517 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0002-8674-1779 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0002-5366-4156 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0003-0477-0152 | pt_BR |
Appears in Collections: | Artigo de Periódico |
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