JOSÉ ANTONIO
GÓMEZ VIDAL
PROFESOR TITULAR DE UNIVERSIDAD
Publications (34) Publications de JOSÉ ANTONIO GÓMEZ VIDAL
2024
2023
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Cytotoxic evaluation of YSL-109 in a triple negative breast cancer cell line and toxicological evaluations
Naunyn-Schmiedeberg's Archives of Pharmacology, Vol. 396, Núm. 6, pp. 1211-1222
2022
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Effectiveness of an O-Alkyl Hydroxamate in Dogs with Naturally Acquired Canine Leishmaniosis: An Exploratory Clinical Trial
Animals, Vol. 12, Núm. 19
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In silico design of HDAC6 inhibitors with neuroprotective effects
Journal of Biomolecular Structure and Dynamics, Vol. 40, Núm. 24, pp. 14204-14222
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New salicylic acid derivatives, double inhibitors of glycolate oxidase and lactate dehydrogenase, as effective agents decreasing oxalate production
European Journal of Medicinal Chemistry, Vol. 237
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Targeting Several Biologically Reported Targets of Glioblastoma Multiforme by Assaying 2D and 3D Cultured Cells
Cellular and Molecular Neurobiology, Vol. 42, Núm. 6, pp. 1909-1920
2021
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Modifications on the tetrahydroquinoline scaffold targeting a phenylalanine cluster on GPER as antiproliferative compounds against renal, liver and pancreatic cancer cells
Pharmaceuticals, Vol. 14, Núm. 1, pp. 1-19
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Small molecule-based enzyme inhibitors in the treatment of primary hyperoxalurias
Journal of Personalized Medicine, Vol. 11, Núm. 2, pp. 1-31
2020
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Hydroxamic acid derivatives as HDAC1, HDAC6 and HDAC8 inhibitors with antiproliferative activity in cancer cell lines
Scientific Reports, Vol. 10, Núm. 1
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O-Alkyl Hydroxamates Display Potent and Selective Antileishmanial Activity
Journal of Medicinal Chemistry, Vol. 63, Núm. 11, pp. 5734-5751
2019
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A nanodelivered Vorinostat derivative is a promising oral compound for the treatment of visceral leishmaniasis
Pharmacological Research, Vol. 139, pp. 375-383
2018
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Salicylic Acid Derivatives Inhibit Oxalate Production in Mouse Hepatocytes with Primary Hyperoxaluria Type 1
Journal of Medicinal Chemistry, Vol. 61, Núm. 16, pp. 7144-7167
2017
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Searching the conformational complexity and binding properties of HDAC6 through docking and molecular dynamic simulations
Journal of Biomolecular Structure and Dynamics, Vol. 35, Núm. 13, pp. 2794-2814
2014
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Exploring the potential binding sites of some known HDAC inhibitors on some HDAC8 conformers by docking studies
Applied Biochemistry and Biotechnology, Vol. 173, Núm. 7, pp. 1907-1926
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Production of the Phanerochaete flavido-alba laccase in Aspergillus niger for synthetic dyes decolorization and biotransformation
World Journal of Microbiology and Biotechnology, Vol. 30, Núm. 1, pp. 201-211
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Synthesis of l -octaarginine through microencapsulated palladium-catalyzed allyl ester deprotection
Synlett, Vol. 25, Núm. 16, pp. 2319-2322
2013
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Estudio de la estabilidad de tiaprida en disolución para administración en perfusión intravenosa continua
Farmacia Hospitalaria, Vol. 37, Núm. 1, pp. 10-14
2008
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Anticancer activity of (1,2,3,5-tetrahydro-4,1-benzoxazepine-3-yl)-pyrimidines and -purines against the MCF-7 cell line: Preliminary cDNA microarray studies
Bioorganic and Medicinal Chemistry Letters, Vol. 18, Núm. 4, pp. 1457-1460
2007
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5-fluorouracil derivatives induce differentiation mediated by tubulin and HLA class I modulation
Medicinal Chemistry, Vol. 3, Núm. 3, pp. 233-239
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A synthetic uracil derivative with antitumor activity through decreasing cyclin D1 and Cdk1, and increasing p21 and p27 in MCF-7 cells
Breast Cancer Research and Treatment, Vol. 105, Núm. 3, pp. 237-246