<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-29T09:28:11Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/12634" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/12634</identifier><datestamp>2024-10-01T14:24:01Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Evaluation of the Antioxidant and Neuroprotectant Activities of New Asymmetrical 1,3-Diketones</dc:title>
   <dc:creator>Nieto, Carla</dc:creator>
   <dc:creator>Cornago, María</dc:creator>
   <dc:creator>Cabildo, María</dc:creator>
   <dc:creator>Sanz, Dionisia</dc:creator>
   <dc:creator>Claramunt, Rosa</dc:creator>
   <dc:creator>Torralba Martínez, María Del Carmen</dc:creator>
   <dc:creator>Torres, María del Rosario</dc:creator>
   <dc:creator>Martínez Casanova, Diana</dc:creator>
   <dc:creator>Sánchez-Alegre, Yaiza</dc:creator>
   <dc:creator>Escudero, Esther</dc:creator>
   <dc:creator>Lavandera, José</dc:creator>
   <dc:subject>neurodegeneration</dc:subject>
   <dc:subject>oxidative stress</dc:subject>
   <dc:subject>neuroprotectant</dc:subject>
   <dc:subject>antioxidant</dc:subject>
   <dc:subject>β-diketones</dc:subject>
   <dc:subject>drug-like properties</dc:subject>
   <dc:subject>Química inorgánica (Química)</dc:subject>
   <dc:subject>2303 Química Inorgánica</dc:subject>
   <dc:description>A series of fourteen new asymmetrical 1,3-diketone derivatives have been synthesized and evaluated in the ABTS, FRAP and DPPH assays as a new chemotype with antioxidant and drug-like properties. All the compounds displayed low cytotoxicity in comparison to curcumin against the human neuroblastoma SH-SY5Y cell line. Among them, (3Z,5E)-6-(2,5-difluoro-4-hydroxy-phenyl)-1,1,1-trifluoro-4-hydroxyhexa-3,5-dien-2-one (6b) and (3Z,5E)-6-(2,3-difluoro-4-hydroxy-phenyl)-1,1,1-trifluoro-4-hydroxyhexa-3,5-dien-2-one (7b) with excellent solubility and chemical stability in biorelevant media, have also shown a similar Fe+2 chelation behavior to that of curcumin. Additionally, both derivatives 6b and 7b have afforded good neuroprotection activity against H2O2 induced oxidative stress in the same neuronal cell line, with a significant reduction of intracellular ROS levels, in parallel with a good recovery of the Mitochondrial Membrane Potential (ΔΨm). Compounds 6b and 7b with a promising antioxidant and drug-like profile, with low cytotoxic and good neuroprotectant activity, constitute a new interesting chemical class with high potential as new therapeutic agents against neurodegenerative diseases.</dc:description>
   <dc:description>Ministerio de Economía y Competitividad (MINECO)</dc:description>
   <dc:description>Depto. de Química Inorgánica</dc:description>
   <dc:description>Fac. de Ciencias Químicas</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2023-06-17T12:37:09Z</dc:date>
   <dc:date>2023-06-17T12:37:09Z</dc:date>
   <dc:date>2018-07-24</dc:date>
   <dc:type>journal article</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/12634</dc:identifier>
   <dc:identifier>1420-3049</dc:identifier>
   <dc:identifier>10.3390/molecules23081837</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>CTQ2014-56833-R</dc:relation>
   <dc:rights>Atribución 3.0 España</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by/3.0/es/</dc:rights>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>MDPI</dc:publisher>
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