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Vincent Théry

Researcher at University of Auvergne

Publications -  42
Citations -  1191

Vincent Théry is an academic researcher from University of Auvergne. The author has contributed to research in topics: Catalysis & Kinase. The author has an hindex of 16, co-authored 41 publications receiving 1081 citations. Previous affiliations of Vincent Théry include Blaise Pascal University & Centre national de la recherche scientifique.

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Quantum mechanical computations on very large molecular systems: the local self-consistent field method

TL;DR: Simulations of large systems, involving local changes of electronic structure, are possible at a good degree of approximation by introducing a quantum chemical part in molecular dynamics studies.
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Click Chelators for Platinum‐Based Anticancer Drugs

TL;DR: In this article, the triazole-amine triazoles from click chemistry are convenient ligands for the formation of platinum complexes bearing combined triazola-amine or triazolara-carboxylate moieties and striking differences in the chelation modes are observed between the two series.
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Synthesis, protein kinase inhibitory potencies, and in vitro antiproliferative activities of meridianin derivatives.

TL;DR: In this paper, the synthesis of new meridianin derivatives is described and the most effective compounds toward these two kinase families are the 6-and 7-bromo derivatives 30, 33, and 34 that showed more than 45fold selectivity toward DYRK1A/CLK1 kinases over the other kinases tested.

Synthesis, protein kinase inhibitory potencies and in vitro antiproliferative activities of meridianin derivatives

TL;DR: The 6- and 7-bromo derivatives 30, 33, and 34 that showed more than 45-fold selectivity toward DYRK1A/CLK1 kinases over the other kinases tested could thus be developed toward potent and selective inhibitors of key RNA splicing regulators and potential therapeutic agents.
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12-Helix folding of cyclobutane beta-amino acid oligomers.

TL;DR: Observations suggest a marked preference for the folding of trans-2-aminocyclobutane carboxylic acid oligomers into a well-defined 12-helical conformation in both solution and the solid state.