QUIBIONAT
Química y Bioactividad de Compuestos basados en Productos Naturales
Publications (38) Publications in which a researcher has participated
2024
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1,2,3-Triazole-totarol conjugates as potent PIP5K1α lipid kinase inhibitors
Bioorganic and Medicinal Chemistry, Vol. 105
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A one-pot and eco-friendly synthesis of novel β-substituted-α-halomethyl acrylates and the bioactivity of these compounds in an in vitro model of mast cell degranulation induced by pro-inflammatory stimuli
Biomedicine and Pharmacotherapy, Vol. 170
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Synthesis, Biological Activity, and Molecular-Docking Studies of New Brassinosteroid Analogs
International Journal of Molecular Sciences, Vol. 25, Núm. 18
2023
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Labdane conjugates protect cardiomyocytes from doxorubicin-induced cardiotoxicity
Drug Development Research, Vol. 84, Núm. 1, pp. 84-95
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Phenolic and quinone methide nor-triterpenes as selective NLRP3 inflammasome inhibitors
Bioorganic Chemistry, Vol. 132
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Synthesis and biological evaluation of anthracene-9,10 dione derivatives as CK2 inhibitors
Results in Chemistry, Vol. 6
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Synthesis of Structurally Related Coumarin Derivatives as Antiproliferative Agents
ACS Omega, Vol. 8, Núm. 29, pp. 26479-26496
2022
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Dehydroisohispanolone as a Promising NLRP3 Inhibitor Agent: Bioevaluation and Molecular Docking
Pharmaceuticals, Vol. 15, Núm. 7
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Design, Semisynthesis, and Estrogenic Activity of Lignan Derivatives from Natural Dibenzylbutyrolactones
Pharmaceuticals, Vol. 15, Núm. 5, pp. 585
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Structure-activity relationships reveal a 2-furoyloxychalcone as a potent cytotoxic and apoptosis inducer for human U-937 and HL-60 leukaemia cells
Bioorganic Chemistry, Vol. 127
2021
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Autodisplay of human PIP5K1α lipid kinase on Escherichia coli and inhibitor testing
Enzyme and Microbial Technology, Vol. 143
2020
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Dehydrohispanolone Derivatives Attenuate the Inflammatory Response through the Modulation of Inflammasome Activation
Journal of Natural Products, Vol. 83, Núm. 7, pp. 2155-2164
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Development of an in vitro screening assay for PIP5K1α lipid kinase and identification of potent inhibitors
FEBS Journal, Vol. 287, Núm. 14, pp. 3042-3064
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The synthetic flavanone 6-methoxy-2-(naphthalen-1-yl)chroman-4-one induces apoptosis and activation of the MAPK pathway in human U-937 leukaemia cells
Bioorganic Chemistry, Vol. 94
2018
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3′-Hydroxy-3,4′-dimethoxyflavone-induced cell death in human leukaemia cells is dependent on caspases and reactive oxygen species and attenuated by the inhibition of JNK/SAPK
Chemico-Biological Interactions, Vol. 288, pp. 1-11
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Semisynthesis and inhibitory effects of solidagenone derivatives on TLR-mediated inflammatory responses
Molecules, Vol. 23, Núm. 12
2017
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3′-Hydroxy-3,4′-dimethoxyflavone blocks tubulin polymerization and is a potent apoptotic inducer in human SK-MEL-1 melanoma cells
Bioorganic and Medicinal Chemistry, Vol. 25, Núm. 21, pp. 6060-6070
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Synthesis and biological evaluation of naphthoquinone-coumarin conjugates as topoisomerase II inhibitors
Bioorganic and Medicinal Chemistry Letters, Vol. 27, Núm. 3, pp. 484-489
2015
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A new iridoid, verbascoside and derivatives with inhibitory activity against Taq DNA polymerase
Bioorganic and Medicinal Chemistry Letters, Vol. 25, Núm. 4, pp. 914-918
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Antiproliferative and structure activity relationships of amaryllidaceae alkaloids
Molecules, Vol. 20, Núm. 8, pp. 13854-13863