Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/42956
Title: Drug Discovery Targeted to Transthyretin Related Amyloidosis
Author: Blasi Pérez, Daniel
Director: Quintana Ruiz, Jordi Ramon
Boada Centeno, Núria
Albericio Palomera, Fernando
Keywords: Transthyretin (TTR)
Transtiretina
Amyloidosis
Amiloïdosi
Amiloidosis
Ligand Efficiency Indices
Índexs d'eficència lligant
Índices de eficiencia ligante
Issue Date: 27-Feb-2013
Publisher: Universitat de Barcelona
Abstract: [eng] Several drug discovery approaches has been performed to find new compounds able to interact with high affinity with the hormone binding site of the homotetrameric protein transthyretin (TTR), and stabilize this tetramer, becoming drug candidates to treat several rare amyloid diseases associated with TTR. With this aim, several computational workflows and chemico-biological databases have been developed, and in collaboration with two experimental research laboratories of our TTR Consortium (one contributing with the chemical synthesis or acquisition of the designed compounds, and the other contributing with the biological activity assay results for the synthesized or acquired compounds). The specific objectives of this thesis are: a) The generation of a chemico-biological database containing the historical and newly generated results of the TTR Consortium, containing the chemical structures and biological activities of the TTR ligands. b) Explore the possibility of using repurposing techniques applied to the discovery of new TTR inhibitors among the existing drugs, with particular focus on anti-inflammatory drugs, which are known to be good TTR ligands. c) Design of new flavonoid compounds as TTR ligands by means of structure-based drug design. d) Incorporate the Ligand Efficiency Indices analysis (both retrospective and prospective) as a new tool for designing new compounds with increased efficiency as TTR ligands. e) The computational development of a combined predictive/experimental workflow for the analysis of the metabolic stability of TTR ligands, as a tool for improving the prioritized compounds in our in-house database to obtain new compounds with better metabolic and pharmacokinetic properties. Among this thesis those workflows have been developed in order to obtain possible new amyloidogenic inhibitors: a) A computational workflow to obtain TTR ligand fingerprints has been developed, and the application of this workflow to the repurposing of marketed antiinflammatory drugs has delivered 3 compounds as new TTR stabilizers. b) A computational workflow to obtain a TTR-protein structure based pharmacophore has been developed, and the application of this workflow to a database of flavonoid compounds has delivered one compound as a new TTR stabilizer.
URI: http://hdl.handle.net/2445/42956
Appears in Collections:Tesis Doctorals - Departament - Química Orgànica

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