Facultade de Farmacia
Fakultät
Columbia University Medical Center
Nueva York, Estados UnidosPublikationen in Zusammenarbeit mit Forschern von Columbia University Medical Center (27)
2022
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Comparative functional genomics identifies unique molecular features of EPSCs
Life Science Alliance, Vol. 5, Núm. 11
2021
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Phase separation of OCT4 controls TAD reorganization to promote cell fate transitions
Cell Stem Cell, Vol. 28, Núm. 10, pp. 1868-1883.e11
2020
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ADAR1-Dependent RNA Editing Promotes MET and iPSC Reprogramming by Alleviating ER Stress
Cell Stem Cell, Vol. 27, Núm. 2, pp. 300-314.e11
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An Optimized Immunoprecipitation Protocol for Assessing Protein-RNA Interactions In Vitro
STAR Protocols, Vol. 1, Núm. 2
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Broad Spectrum project: Factors determining the quality of antibiotic use in primary care: An observational study protocol from Italy
BMJ Open, Vol. 10, Núm. 7
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Functional role of Tet-mediated RNA hydroxymethylcytosine in mouse ES cells and during differentiation
Nature Communications, Vol. 11, Núm. 1
2017
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New insights into highly potent tyrosinase inhibitors based on 3-heteroarylcoumarins: Anti-melanogenesis and antioxidant activities, and computational molecular modeling studies
Bioorganic and Medicinal Chemistry, Vol. 25, Núm. 5, pp. 1687-1695
2016
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Computational Drug Target Screening through Protein Interaction Profiles
Scientific Reports, Vol. 6
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Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond
PLoS Pathogens, Vol. 12, Núm. 7
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Progress in the development of small molecules as new human A3 adenosine receptor ligands based on the 3-thiophenylcoumarin core
MedChemComm, Vol. 7, Núm. 5, pp. 845-852
2015
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Design and discovery of tyrosinase inhibitors based on a coumarin scaffold
RSC Advances, Vol. 5, Núm. 114, pp. 94227-94235
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Development of novel adenosine receptor ligands based on the 3-amidocoumarin scaffold
Bioorganic Chemistry, Vol. 61, pp. 1-6
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Navigating in chromone chemical space: Discovery of novel and distinct A3 adenosine receptor ligands
RSC Advances, Vol. 5, Núm. 96, pp. 78572-78585
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Potent and selective MAO-B inhibitory activity: Amino- versus nitro-3-arylcoumarin derivatives
Bioorganic and Medicinal Chemistry Letters, Vol. 25, Núm. 3, pp. 642-648
2014
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Insight into the functional and structural properties of 3-arylcoumarin as an interesting scaffold in monoamine oxidase B inhibition
ChemMedChem, Vol. 9, Núm. 7, pp. 1488-1500
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Monoamine oxidase (MAO) inhibitory activity: 3-phenylcoumarins versus 4-hydroxy-3-phenylcoumarins
ChemMedChem, Vol. 9, Núm. 8, pp. 1672-1676
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Similarity-based modeling in large-scale prediction of drug-drug interactions
Nature Protocols, Vol. 9, Núm. 9, pp. 2147-2163
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State of the art and development of a drug-drug interaction large scale predictor based on 3D pharmacophoric similarity
Current Drug Metabolism, Vol. 15, Núm. 5, pp. 490-501
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Synthesis, pharmacological study and docking calculations of new benzo[f]coumarin derivatives as dual inhibitors of enzymatic systems involved in neurodegenerative diseases
Future Medicinal Chemistry, Vol. 6, Núm. 4, pp. 371-383
2013
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Comparative study of the 3-phenylcoumarin scaffold: Synthesis, X-ray structural analysis and semiempirical calculations of a selected series of compounds
Journal of Molecular Structure, Vol. 1050, pp. 185-191