Desinfarma
Descubrimento e síntese de fármacos
Publicacións (126) Publicacións nas que participase algún/ha investigador/a
2024
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Benzylhydroxamic acids as inhibitors of insulin regulated aminopeptidase (IRAP)
European Journal of Medicinal Chemistry Reports, Vol. 12
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N-Adamantyl-1-alkyl-4-oxo-1,4-dihydroquinoline-3-carboxamide Derivatives as Fluorescent Probes to Detect Microglia Activation through the Imaging of Cannabinoid Receptor Subtype 2 (CB2R)
Journal of Medicinal Chemistry, Vol. 67, Núm. 13, pp. 11003-11023
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Telescoped One-Pot Strategy for the Assembly of cis-4-Hydroxy-l-Prolyl Amides
ACS Sustainable Chemistry and Engineering, Vol. 12, Núm. 46, pp. 16986-16998
2023
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Development of Fluorescent 4-[4-(3H-Spiro[isobenzofuran-1,4′-piperidin]-1′-yl)butyl]indolyl Derivatives as High-Affinity Probes to Enable the Study of σ Receptors via Fluorescence-Based Techniques
Journal of Medicinal Chemistry, Vol. 66, Núm. 6, pp. 3798-3817
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Multicomponent Reaction-Assisted Drug Discovery: A Time- and Cost-Effective Green Approach Speeding Up Identification and Optimization of Anticancer Drugs
International Journal of Molecular Sciences, Vol. 24, Núm. 7
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N-adamantyl-anthranil amide derivatives: New selective ligands for the cannabinoid receptor subtype 2 (CB2R)
European Journal of Medicinal Chemistry, Vol. 248
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Stapling Amantadine to Melanostatin Neuropeptide: Discovery of Potent Positive Allosteric Modulators of the D2 Receptors
ACS Medicinal Chemistry Letters, Vol. 14, Núm. 12, pp. 1656-1663
2022
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Enantiomeric Separation and Molecular Modelling of Bioactive 4-Aryl-3,4-dihydropyrimidin-2(1H)-one Ester Derivatives on Teicoplanin-Based Chiral Stationary Phase
Separations, Vol. 9, Núm. 1
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Exploring Non-orthosteric Interactions with a Series of Potent and Selective A3Antagonists
ACS Medicinal Chemistry Letters, Vol. 13, Núm. 2, pp. 243-249
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Isolation and structural characterization of stable carbamic-carbonic anhydrides: an experimental and computational study
Organic Chemistry Frontiers, Vol. 9, Núm. 8, pp. 2154-2163
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Optimization of 2-Amino-4,6-diarylpyrimidine-5-carbonitriles as Potent and Selective A1Antagonists
Journal of Medicinal Chemistry, Vol. 65, Núm. 3, pp. 2091-2106
2021
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Discovery of New Potent Positive Allosteric Modulators of Dopamine D2Receptors: Insights into the Bioisosteric Replacement of Proline to 3-Furoic Acid in the Melanostatin Neuropeptide
Journal of Medicinal Chemistry, Vol. 64, Núm. 9, pp. 6209-6220
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Identification of V6.51L as a selectivity hotspot in stereoselective A2B adenosine receptor antagonist recognition
Scientific Reports, Vol. 11, Núm. 1
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Potent and Subtype-Selective Dopamine D2Receptor Biased Partial Agonists Discovered via an Ugi-Based Approach
Journal of Medicinal Chemistry, Vol. 64, Núm. 12, pp. 8710-8726
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Stereoselective Synthesis of Hydrindane and Hydroazulene Derivatives by Transannular Cyclization of Nine- And Ten-Membered Carbocycles
Journal of Organic Chemistry, Vol. 86, Núm. 19, pp. 13684-13692
2020
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A sustainable strategy for the assembly of Glypromate® and its structurally-related analogues by tandem sequential peptide coupling
Green Chemistry, Vol. 22, Núm. 11, pp. 3584-3596
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Nitrogen-Walk Approach to Explore Bioisosteric Replacements in a Series of Potent A2B Adenosine Receptor Antagonists
Journal of medicinal chemistry, Vol. 63, Núm. 14, pp. 7721-7739
2019
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Mechanistic insights for the transprotection of tertiary amines with Boc2O: Via charged carbamates: Access to both enantiomers of 2-azanorbornane-3- exo -carboxylic acids
Organic Chemistry Frontiers, Vol. 6, Núm. 20, pp. 3540-3554
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Multicatalysis Combining 3D-Printed Devices and Magnetic Nanoparticles in One-Pot Reactions: Steps Forward in Compartmentation and Recyclability of Catalysts
ACS Applied Materials and Interfaces, Vol. 11, Núm. 28, pp. 25283-25294
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Trifluorinated Pyrimidine-Based A2B Antagonists: Optimization and Evidence of Stereospecific Recognition
Journal of Medicinal Chemistry, Vol. 62, Núm. 20, pp. 9315-9330