José Manuel
Brea Floriani
Profesor titular de universidade
MARIA DE LOS ANGELES
CASTRO PEREZ
Profesora titular de universidade
Publicacións nas que colabora con MARIA DE LOS ANGELES CASTRO PEREZ (19)
2024
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2-Aryladenine Derivatives as a Potent Scaffold for Adenosine Receptor Antagonists: The 6-Morpholino Derivatives
Molecules, Vol. 29, Núm. 11
2022
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An Experience of Using a Canvas-Based Template for Blended-Learning in a Master in Drug Discovery
International Journal of Emerging Technologies in Learning, Vol. 17, Núm. 6, pp. 257-267
2020
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Essential role of the C148–C227 disulphide bridge in the human 5-HT2A homodimeric receptor
Biochemical Pharmacology, Vol. 177
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New serotoninergic ligands containing indolic and methyl indolic nuclei: Synthesis and in vitro pharmacological evaluation
Medicinal Chemistry, Vol. 16, Núm. 4, pp. 517-530
2019
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2-Aryladenine derivatives as a potent scaffold for A1, A3 and dual A1/A3 adenosine receptor antagonists: Synthesis and structure-activity relationships
Bioorganic and Medicinal Chemistry, Vol. 27, Núm. 16, pp. 3551-3558
2017
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Development of Fluorescent Probes that Target Serotonin 5-HT2B Receptors
Scientific Reports, Vol. 7, Núm. 1
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Serotonin 2A receptor disulfide bridge integrity is crucial for ligand binding to different signalling states but not for its homodimerization
European Journal of Pharmacology, Vol. 815, pp. 138-146
2016
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8-Aminomethyl-7-hydroxy-4-methylcoumarins as Multitarget Leads for Alzheimer's Disease
ChemistrySelect, Vol. 1, Núm. 11, pp. 2742-2749
2015
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Computer-aided structure-based design of multitarget leads for Alzheimer's disease
Journal of Chemical Information and Modeling, Vol. 55, Núm. 1, pp. 135-148
2014
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Novel insights on the structural determinants of clozapine and olanzapine multi-target binding profiles
European Journal of Medicinal Chemistry, Vol. 77, pp. 91-95
2013
2012
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New chromene scaffolds for adenosine A2A receptors: Synthesis, pharmacology and structure-activity relationships
European Journal of Medicinal Chemistry, Vol. 54, pp. 303-310
2011
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Synthesis of novel chromene scaffolds for adenosine receptors
Organic and Biomolecular Chemistry, Vol. 9, Núm. 11, pp. 4242-4249
2010
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Identification of novel species-selective agonists of the G-protein-coupled receptor GPR35 that promote recruitment of β-arrestin-2 and activate Gα13
Biochemical Journal, Vol. 432, Núm. 3, pp. 451-459
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Phe369(7.38) at human 5-HT 7 receptors confers interspecies selectivity to antagonists and partial agonists
British Journal of Pharmacology, Vol. 159, Núm. 5, pp. 1069-1081
2009
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Evidence for distinct antagonist-revealed functional states of 5-hydroxytryptamine2A receptor homodimers
Molecular Pharmacology, Vol. 75, Núm. 6, pp. 1380-1391
2008
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A new chemical tool (C0036E08) supports the role of adenosine A2B receptors in mediating human mast cell activation
Biochemical Pharmacology, Vol. 76, Núm. 7, pp. 912-921
2006
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Parallel regulation by olanzapine of the patterns of expression of 5-HT2A and D3 receptors in rat central nervous system and blood cells
Neuropharmacology, Vol. 51, Núm. 4, pp. 923-932
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QF2004B, a potential antipsychotic butyrophenone derivative with similar pharmacological properties to clozapine
Neuropharmacology, Vol. 51, Núm. 2, pp. 251-262