Works matching AU De Filippis, Barbara
Results: 50
New azolyl-derivatives as multitargeting agents against breast cancer and fungal infections: synthesis, biological evaluation and docking study.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 1631, doi. 10.1080/14756366.2021.1954918
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Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1400, doi. 10.1080/14756366.2019.1651315
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Fibrate-based N-acylsulphonamides targeting carbonic anhydrases: synthesis, biochemical evaluation, and docking studies.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1051, doi. 10.1080/14756366.2019.1611801
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- Article
CAPE and Neuroprotection: A Review.
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- Biomolecules (2218-273X), 2021, v. 11, n. 2, p. 176, doi. 10.3390/biom11020176
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CAPE synthetic derivatives and their potential role in skin regeneration.
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- Italian Journal of Anatomy & Embryology / Archivio Italiano di Anatomia Ed Embriologia, 2021, v. 125, p. 104
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Candida rugosa lipase-catalysed kinetic resolution of 2-substituted-aryloxyacetic esters with dimethylsulfoxide and isopropanol as additives.
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- Chirality, 2008, v. 20, n. 2, p. 115, doi. 10.1002/chir.20505
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QSAR, QSPR and QSRR in Terms of 3-D-MoRSE Descriptors for In Silico Screening of Clofibric Acid Analogues.
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- Molecular Informatics, 2012, v. 31, n. 6/7, p. 453, doi. 10.1002/minf.201200001
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Titanium-Promoted Acylation of Sulfonamides to N -Acylsulfonamide PPAR α Antagonists.
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- Synthetic Communications, 2015, v. 45, n. 22, p. 2546, doi. 10.1080/00397911.2015.1092552
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Stilbene derivatives as new perspective in antifungal medicinal chemistry.
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- Drug Development Research, 2019, v. 80, n. 3, p. 285, doi. 10.1002/ddr.21525
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Geometric Isomerism of an Acetamidino Derivative Determined by NMR Investigations.
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- ChemistrySelect, 2017, v. 2, n. 30, p. 9706, doi. 10.1002/slct.201701646
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N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 6, p. 1094, doi. 10.1111/cbdd.13043
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Cytotoxic effect of a family of peroxisome proliferator-activated receptor antagonists in colorectal and pancreatic cancer cell lines.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 5, p. 1029, doi. 10.1111/cbdd.13026
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Synthesis of Naphthyl-, Quinolin- and Anthracenyl Analogues of Clofibric Acid as PPAR α Agonists.
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- Chemical Biology & Drug Design, 2016, v. 87, n. 3, p. 467, doi. 10.1111/cbdd.12677
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Synthesis of diastereomerically enriched 2-bromoesters and their reaction with nucleophiles.
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- Chirality, 2001, v. 13, n. 2, p. 102, doi. 10.1002/1520-636X(2001)13:2<102::AID-CHIR1005>3.0.CO;2-E
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Synthesis of 2-aryloxy acids analogues of clofibrate via dynamic kinetic resolution.
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- Chirality, 1999, v. 11, n. 5/6, p. 483, doi. 10.1002/(SICI)1520-636X(1999)11:5/6<483::AID-CHIR21>3.0.CO;2-I
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Development of Fibrates as Important Scaffolds in Medicinal Chemistry.
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- ChemMedChem, 2019, v. 14, n. 11, p. 1051, doi. 10.1002/cmdc.201900128
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Anticancer Activity of Stilbene-Based Derivatives.
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- ChemMedChem, 2017, v. 12, n. 8, p. 558, doi. 10.1002/cmdc.201700045
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Indazole, Pyrazole, and Oxazole Derivatives Targeting Nitric Oxide Synthases and Carbonic Anhydrases.
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- ChemMedChem, 2016, v. 11, n. 16, p. 1695, doi. 10.1002/cmdc.201600204
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Blocking the Peroxisome Proliferator-Activated Receptor (PPAR): An Overview.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1609, doi. 10.1002/cmdc.201300250
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Selective Inhibition of iNOS by Benzyl- and Dibenzyl Derivatives of N-(3-Aminobenzyl)acetamidine.
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- ChemMedChem, 2011, v. 6, n. 7, p. 1203, doi. 10.1002/cmdc.201100125
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Advancements in the Research of New Modulators of Nitric Oxide Synthases Activity.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 15, p. 8486, doi. 10.3390/ijms25158486
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Anticancer Activity of Natural Products and Related Compounds.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 22, p. 16507, doi. 10.3390/ijms242216507
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Emerging Effects of Resveratrol Derivatives in Cells Involved in Oral Wound Healing: A Preliminary Study.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3276, doi. 10.3390/ijms24043276
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Resveratrol Derivative Exhibits Marked Antiproliferative Actions, Affecting Stemness in Pancreatic Cancer Cells.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 1977, doi. 10.3390/ijms24031977
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The Selective Acetamidine-Based iNOS Inhibitor CM544 Reduces Glioma Cell Proliferation by Enhancing PARP-1 Cleavage In Vitro.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 3, p. 495, doi. 10.3390/ijms20030495
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Seeking for Non-Zinc-Binding MMP-2 Inhibitors: Synthesis, Biological Evaluation and Molecular Modelling Studies.
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- International Journal of Molecular Sciences, 2016, v. 17, n. 10, p. 1768, doi. 10.3390/ijms17101768
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Reversed-phase high-performance liquid chromatography method with fluorescence detection to screen nitric oxide synthases inhibitors.
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- Journal of Separation Science, 2014, v. 37, n. 12, p. 1380, doi. 10.1002/jssc.201400059
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- Article
Azobenzene as Multi-Targeted Scaffold in Medicinal Chemistry.
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- Molecules, 2024, v. 29, n. 24, p. 5872, doi. 10.3390/molecules29245872
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Radiolabeled Probes from Derivatives of Natural Compounds Used in Nuclear Medicine.
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- Molecules, 2024, v. 29, n. 17, p. 4260, doi. 10.3390/molecules29174260
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- Article
Resveratrol Analogues as Dual Inhibitors of Monoamine Oxidase B and Carbonic Anhydrase VII: A New Multi-Target Combination for Neurodegenerative Diseases?
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- Molecules, 2022, v. 27, n. 22, p. 7816, doi. 10.3390/molecules27227816
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The Small Molecule PPARγ Agonist GL516 Induces Feeding-Stimulatory Effects in Hypothalamus Cells Hypo-E22 and Isolated Hypothalami.
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- Molecules, 2022, v. 27, n. 15, p. 4882, doi. 10.3390/molecules27154882
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Delivery of Thyronamines (TAMs) to the Brain: A Preliminary Study.
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- Molecules, 2021, v. 26, n. 6, p. 1616, doi. 10.3390/molecules26061616
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Development of CDK4/6 Inhibitors: A Five Years Update.
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- Molecules, 2021, v. 26, n. 5, p. 1488, doi. 10.3390/molecules26051488
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Parameters for Irreversible Inactivation of Monoamine Oxidase.
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- Molecules, 2020, v. 25, n. 24, p. 5908, doi. 10.3390/molecules25245908
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Synthesis and Biological Evaluation of Halogenated E -Stilbenols as Promising Antiaging Agents.
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- Molecules, 2020, v. 25, n. 23, p. 5770, doi. 10.3390/molecules25235770
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- Article
Laquinimod Modulates Human Astrocyte Function and Dampens Astrocyte-Induced Neurotoxicity during Inflammation.
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- Molecules, 2020, v. 25, n. 22, p. 5403, doi. 10.3390/molecules25225403
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- Article
Design, Synthesis, and Biological Evaluation of Pyridazinones Containing the (2-Fluorophenyl) Piperazine Moiety as Selective MAO-B Inhibitors.
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- Molecules, 2020, v. 25, n. 22, p. 5371, doi. 10.3390/molecules25225371
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- Article
Anti-aggregation Effects of Phenolic Compounds on α-synuclein.
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- Molecules, 2020, v. 25, n. 10, p. 2444, doi. 10.3390/molecules25102444
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Development of a Rapid Mass Spectrometric Determination of AMP and Cyclic AMP for PDE3 Activity Study: Application and Computational Analysis for Evaluating the Effect of a Novel 2-oxo-1,2-dihydropyridine-3-carbonitrile Derivative as PDE-3 Inhibitor.
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- Molecules, 2020, v. 25, n. 8, p. 1817, doi. 10.3390/molecules25081817
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- Article
Azobenzenesulfonamide Carbonic Anhydrase Inhibitors as New Weapons to Fight Helicobacter pylori : Synthesis, Bioactivity Evaluation, In Vivo Toxicity, and Computational Studies.
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- Pharmaceuticals (14248247), 2024, v. 17, n. 8, p. 1027, doi. 10.3390/ph17081027
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Anti-Inflammatory, Antioxidant, and WAT/BAT-Conversion Stimulation Induced by Novel PPAR Ligands: Results from Ex Vivo and In Vitro Studies.
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- Pharmaceuticals (14248247), 2023, v. 16, n. 3, p. 346, doi. 10.3390/ph16030346
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Nitrostilbenes: Synthesis and Biological Evaluation as Potential Anti-Influenza Virus Agents.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 9, p. N.PAG, doi. 10.3390/ph15091061
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- Article
Benzothiazole Derivatives Endowed with Antiproliferative Activity in Paraganglioma and Pancreatic Cancer Cells: Structure–Activity Relationship Studies and Target Prediction Analysis.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 8, p. 937, doi. 10.3390/ph15080937
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HDAC Inhibitors for the Therapy of Triple Negative Breast Cancer.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 6, p. 667, doi. 10.3390/ph15060667
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Design, Synthesis and Biological Evaluation of Aromatase Inhibitors Based on Sulfonates and Sulfonamides of Resveratrol.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 10, p. 984, doi. 10.3390/ph14100984
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- Article
CAPE derivatives: Multifaceted agents for chronic wound healing.
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- Archiv der Pharmazie, 2024, v. 357, n. 10, p. 1, doi. 10.1002/ardp.202400165
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Synthesis and in vitro cytotoxicity of benzoxazole‐based PPARα/γ antagonists in colorectal cancer cell lines.
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- Archiv der Pharmazie, 2024, v. 357, n. 9, p. 1, doi. 10.1002/ardp.202400086
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- Article
Azole-Based Compounds That Are Active against Candida Biofilm: In Vitro , In Vivo and In Silico Studies.
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- Antibiotics (2079-6382), 2022, v. 11, n. 10, p. N.PAG, doi. 10.3390/antibiotics11101375
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Searching for New Tools to Counteract the Helicobacter pylori Resistance: The Positive Action of Resveratrol Derivatives.
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- Antibiotics (2079-6382), 2020, v. 9, n. 12, p. 891, doi. 10.3390/antibiotics9120891
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The Application of Resveratrol Derivatives in Oral Cells Reduces the Oxidative Stress Induced by Glucocorticoids.
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- Metabolites (2218-1989), 2024, v. 14, n. 7, p. 350, doi. 10.3390/metabo14070350
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