Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2024Potential antiprostatic performance of novel lanthanide-complexes based on 5-nitropicolinic acid1citations

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Chart of shared publication
Vitórica-Yrezábal, Iñigo J.
1 / 1 shared
Hidalgo, Tania
1 / 1 shared
Horcajada, Patricia
1 / 15 shared
Rodríguez-Diéguez, Antonio
1 / 7 shared
García-García, Amalia
1 / 2 shared
Rojas, Sara
1 / 6 shared
Chart of publication period
2024

Co-Authors (by relevance)

  • Vitórica-Yrezábal, Iñigo J.
  • Hidalgo, Tania
  • Horcajada, Patricia
  • Rodríguez-Diéguez, Antonio
  • García-García, Amalia
  • Rojas, Sara
OrganizationsLocationPeople

article

Potential antiprostatic performance of novel lanthanide-complexes based on 5-nitropicolinic acid

  • Vitórica-Yrezábal, Iñigo J.
  • Cristobal-Cueto, Pablo
  • Hidalgo, Tania
  • Horcajada, Patricia
  • Rodríguez-Diéguez, Antonio
  • García-García, Amalia
  • Rojas, Sara
Abstract

<jats:title>Abstract</jats:title><jats:p>Two new lanthanide-complexes based on the 5-nitropicolinate ligand (5-npic) were obtained and fully characterized. Single-crystal X-ray diffraction revealed that these compounds are isostructural to a Dy-complex, previously published by us, based on dinuclear monomers link together with an extended hydrogen bond network, providing a final chemical formula of [Ln<jats:sub>2</jats:sub>(5-npic)<jats:sub>6</jats:sub>(H<jats:sub>2</jats:sub>O)<jats:sub>4</jats:sub>]·(H<jats:sub>2</jats:sub>O)<jats:sub>2</jats:sub>, where Ln = Dy <jats:bold>(1)</jats:bold>, Gd <jats:bold>(2)</jats:bold>, and Tb <jats:bold>(3)</jats:bold>. Preliminary photoluminescent studies exhibited a ligand-centered emission for all complexes. The potential antitumoral activity of these materials was assayed in a prostatic cancer cell line (PC-3; the 2nd most common male cancerous disease), showing a significant anticancer activity (50–60% at 500 μg·mL<jats:sup>−1</jats:sup>). In turn, a high biocompatibility by both, the complexes and their precursors in human immunological HL-60 cells, was evidenced. In view of the strongest toxic effect in the tumoral cell line provided by the free 5-npic ligand (~ 40–50%), the overall anticancer complex performance seems to be triggered by the presence of this molecule.</jats:p><jats:p><jats:bold>Graphical Abstract</jats:bold></jats:p>

Topics
  • compound
  • x-ray diffraction
  • Hydrogen
  • Lanthanide
  • biocompatibility