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Andreia Valente

Researcher at University of Lisbon

Publications -  54
Citations -  1439

Andreia Valente is an academic researcher from University of Lisbon. The author has contributed to research in topics: Ruthenium & Chain transfer. The author has an hindex of 20, co-authored 48 publications receiving 1190 citations. Previous affiliations of Andreia Valente include university of lille & Centre national de la recherche scientifique.

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Unprecedented collateral sensitivity for cisplatin-resistant lung cancer cells presented by new ruthenium organometallic compounds

TL;DR: These are the first ruthenium-based compounds with such a mechanism of action, taking advantage of an “Achilles’ heel” and acting as MDR-selective compounds.
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Silica-Grafted Lanthanum Benzyl Species: Synthesis, Characterization, and Catalytic Applications

TL;DR: The grafting of a lanthanum trisbenzyl derivative onto dehydroxylated silica affords a mixture of [(SiO)2La(CH2Ph)(THF)n] and [(≡SiO]La( CH2Ph)2(THFm] surface sites, in respective proportions of 80 and 20%, as evidenced from mass balance analyses, IR and 1H, 13C and 29Si 1D and 2D solid-state NMR spectroscopy as mentioned in this paper.
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Ruthenium carboranyl complexes with 2,2′-bipyridine derivatives for potential bimodal therapy application

TL;DR: In this paper, the ruthenium-carboranyl complexes bearing bipyridyl derivatives with the general formula [3-CO-3,3-{κ2-4,4′-R2-2,2′-bipy}-closo-3-1,2-RuC2B9H11] were crystallized in the monoclinic system, showing the expected three-legged piano stool structure.
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New Cyclams and Their Copper(II) and Iron(III) Complexes: Synthesis and Potential Application as Anticancer Agents.

TL;DR: Compounds containing 4-CF3 PhCH2 pendant arms on the cyclam ring revealed the most activity, with cytotoxicity values up to 12 times higher than those of cisplatin.
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A novel screening method for transition metal-based anticancer compounds using zebrafish embryo-larval assay and inductively coupled plasma-mass spectrometry analysis.

TL;DR: It is proposed that zebrafish embryo‐larval assays coupled with ICPMS serve as a powerful platform to evaluate relative potency and toxic effects of metallodrug candidates.