JOSÉ ÁNGEL
MORALES GARCÍA
Profesor titular de universidad
Instituto de Química Médica
Madrid, EspañaPublications in collaboration with researchers from Instituto de Química Médica (23)
2024
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Discovery of a potent melatonin-based inhibitor of quinone reductase-2 with neuroprotective and neurogenic properties
European Journal of Medicinal Chemistry, Vol. 277
2022
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Resveratrol-Based MTDLs to Stimulate Defensive and Regenerative Pathways and Block Early Events in Neurodegenerative Cascades
Journal of Medicinal Chemistry, Vol. 65, Núm. 6, pp. 4727-4751
2020
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Tuning melatonin receptor subtype selectivity in oxadiazolone-based analogues: Discovery of QR2 ligands and NRF2 activators with neurogenic properties
European Journal of Medicinal Chemistry, Vol. 190
2019
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New flavonoid–N,N-dibenzyl(N-methyl)amine hybrids: Multi-target-directed agents for Alzheimer´s disease endowed with neurogenic properties
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol. 34, Núm. 1, pp. 712-727
2018
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Neurogenic and neuroprotective donepezil-flavonoid hybrids with sigma-1 affinity and inhibition of key enzymes in Alzheimer's disease
European Journal of Medicinal Chemistry, Vol. 156, pp. 534-553
2017
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Subtly Modulating Glycogen Synthase Kinase 3 β: Allosteric Inhibitor Development and Their Potential for the Treatment of Chronic Diseases
Journal of Medicinal Chemistry, Vol. 60, Núm. 12, pp. 4983-5001
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The alkaloids of Banisteriopsis caapi, the plant source of the Amazonian hallucinogen Ayahuasca, stimulate adult neurogenesis in vitro
Scientific Reports, Vol. 7, Núm. 1
2016
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New cinnamic - N-benzylpiperidine and cinnamic - N,N-dibenzyl(N-methyl)amine hybrids as Alzheimer-directed multitarget drugs with antioxidant, cholinergic, neuroprotective and neurogenic properties
European Journal of Medicinal Chemistry, Vol. 121, pp. 376-386
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New neurogenic lipoic-based hybrids as innovative Alzheimer's drugs with σ-1 agonism and β-secretase inhibition
Future Medicinal Chemistry, Vol. 8, Núm. 11, pp. 1191-1207
2015
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Neurogenic potential assessment and pharmacological characterization of 6-Methoxy-1,2,3,4-tetrahydro-β-carboline (Pinoline) and Melatonin-Pinoline Hybrids
ACS Chemical Neuroscience, Vol. 6, Núm. 5, pp. 800-810
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Novel N -Acetyl Bioisosteres of Melatonin: Melatonergic Receptor Pharmacology, Physicochemical Studies, and Phenotypic Assessment of Their Neurogenic Potential
Journal of Medicinal Chemistry, Vol. 58, Núm. 12, pp. 4998-5014
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PDE7 inhibitor TC3.6 ameliorates symptomatology in a model of primary progressive multiple sclerosis
British Journal of Pharmacology, Vol. 172, Núm. 17, pp. 4277-4290
2014
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Crosstalk between phosphodiesterase 7 and glycogen synthase kinase-3: Two relevant therapeutic targets for neurological disorders
ACS Chemical Neuroscience, Vol. 5, Núm. 3, pp. 194-204
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Modulation of cAMP-specific PDE without emetogenic activity: New sulfide-like PDE7 inhibitors
Journal of Medicinal Chemistry, Vol. 57, Núm. 20, pp. 8590-8607
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New melatonin- N, N -dibenzyl(N -methyl)amine hybrids: Potent neurogenic agents with antioxidant, cholinergic, and neuroprotective properties as innovative drugs for alzheimers disease
Journal of Medicinal Chemistry, Vol. 57, Núm. 9, pp. 3773-3785
2013
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Glycogen synthase kinase-3 inhibitors as potent therapeutic agents for the treatment of Parkinson disease
ACS Chemical Neuroscience, Vol. 4, Núm. 2, pp. 350-360
2012
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5-Imino-1,2,4-thiadiazoles: First small molecules As substrate competitive inhibitors of glycogen synthase kinase 3
Journal of Medicinal Chemistry, Vol. 55, Núm. 4, pp. 1645-1661
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Effect of phosphodiesterase 7 (PDE7) inhibitors in experimental autoimmune encephalomyelitis mice. Discovery of a new chemically diverse family of compounds
Journal of Medicinal Chemistry, Vol. 55, Núm. 7, pp. 3274-3284
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Glycogen synthase kinase 3 inhibition promotes adult hippocampal neurogenesis in vitro and in vivo
ACS Chemical Neuroscience, Vol. 3, Núm. 11, pp. 963-971
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Microwave-assisted synthesis of hydroxyphenyl nitrones with protective action against oxidative stress
European Journal of Medicinal Chemistry, Vol. 58, pp. 44-49