Data from: Mononuclear Pd(II) and Pt(II) complexes with an α-N-heterocyclic thiosemicarbazone: cytotoxicity, solution behaviour and interaction <i>versus</i> proven models from biological media

Two Pd(II) and Pt(II) complexes with two pyrrol-2-carbaldehyde N-p-chlorophenylthiosemicarbazone ligands are designed and characterized showing mononuclear structures. An important pharmacological property for both compounds is the high selectivity for tumor cells and a lack of activity in healthy c...

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Detalles Bibliográficos
Autores principales: Matesanz, Ana I., Jimenez Faraco, Eva, Ruiz, María Carolina, Balsa, Lucía Mariana, Navarro Ranninger, Carmen, León, Ignacio Esteban, Quiroga, Adoración G.
Formato: Conjunto de datos
Lenguaje:Inglés
Publicado: 2020
Materias:
Ciencias Exactas
Química
https://purl.org/becyt/ford/1.4
mononuclear structures
biological interactions
Pd(II) complex
Pt(II) complex
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/109060
https://doi.org/10.35537/10915/109060
Aporte de:
SEDICI (UNLP) de Universidad Nacional de La Plata
Descripción
Sumario:Two Pd(II) and Pt(II) complexes with two pyrrol-2-carbaldehyde N-p-chlorophenylthiosemicarbazone ligands are designed and characterized showing mononuclear structures. An important pharmacological property for both compounds is the high selectivity for tumor cells and a lack of activity in healthy cells. The Pd(II) compound shows a higher antitumor activity and selectivity than the Pt(II) compound. Both complexes present a variety of biological interactions: with DNA models (pBR322 and CT DNA), proteins (lysozyme and RNase) and other biological targets like proteosome. Our results show that the Pd(II) complex is a more interesting candidate for potential anticancer therapies than the Pt(II) complex, and we provide new insight into the design and synthesis of palladium compounds as potential antitumor agents.

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