| Nome |
# |
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HDAC Inhibitors for the Therapy of Triple Negative Breast Cancer, file 6da8c85a-7489-4c52-8d9d-a10f318a0a66
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103
|
|
Anticancer Activity of Stilbene-Based Derivatives, file e4233f19-2033-2860-e053-6605fe0a460a
|
75
|
|
Design, synthesis and biological evaluation of aromatase inhibitors based on sulfonates and sulfonamides of resveratrol, file e4233f18-7e82-2860-e053-6605fe0a460a
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43
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|
null, file e4233f18-a76a-2860-e053-6605fe0a460a
|
38
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|
Sulfonimide and Amide Derivatives as Novel PPARα Antagonists: Synthesis, Antiproliferative Activity, and Docking Studies, file e4233f17-d995-2860-e053-6605fe0a460a
|
33
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|
Antiglioma Activity of Aryl and Amido-Aryl Acetamidine Derivatives Targeting iNOS: Synthesis and Biological Evaluation, file e4233f17-b301-2860-e053-6605fe0a460a
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31
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Novel Phenyldiazenyl Fibrate Analogues as PPAR α/γ/δ Pan-Agonists for the Amelioration of Metabolic Syndrome, file e4233f18-b852-2860-e053-6605fe0a460a
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31
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Synthesis and biological characterization of 3-(imidazol-1-ylmethyl)piperidine sulfonamides as aromatase inhibitors, file e4233f19-4794-2860-e053-6605fe0a460a
|
29
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Benzothiazole Derivatives Endowed with Antiproliferative Activity in Paraganglioma and Pancreatic Cancer Cells: Structure-Activity Relationship Studies and Target Prediction Analysis, file 478db8d9-4fef-42b4-bcca-3e36eb51aef6
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28
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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, file e4233f17-ad61-2860-e053-6605fe0a460a
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28
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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, file 4073d51e-af0a-47d7-9c54-966bee986d14
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27
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|
Different binding and recognition modes of GL479, a dual agonist of Peroxisome Proliferator-Activated Receptor α/γ, file e4233f19-55eb-2860-e053-6605fe0a460a
|
22
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|
Fibrate-based N-acylsulphonamides targeting carbonic anhydrases: synthesis, biochemical evaluation, and docking studies, file e4233f18-7444-2860-e053-6605fe0a460a
|
21
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|
Selective Acetamidine-Based Nitric Oxide Synthase Inhibitors: Synthesis, Docking, and Biological Studies, file e4233f17-f40c-2860-e053-6605fe0a460a
|
16
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|
Identification of new anti-Candida compounds by ligand-based pharmacophore virtual screening, file e4233f15-b510-2860-e053-6605fe0a460a
|
14
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Synthesis and Biological Evaluation of Halogenated E-Stilbenols as Promising Antiaging Agents, file e4233f18-1ae2-2860-e053-6605fe0a460a
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12
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New azolyl-derivatives as multitargeting agents against breast cancer and fungal infections: synthesis, biological evaluation and docking study, file e4233f18-7ec0-2860-e053-6605fe0a460a
|
12
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|
Screening of NOS activity and selectivity of newly synthesized acetamidines using RP-HPLC, file e4233f19-2472-2860-e053-6605fe0a460a
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12
|
|
Structural development studies of PPARs ligands based on tyrosine scaffold, file e4233f16-fdf5-2860-e053-6605fe0a460a
|
10
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|
Discovery of N-{3-[(ethanimidoylamino)methyl]benzyl}-L-prolinamide dihydrochloride:
A new potent and selective inhibitor of the inducible nitric oxide synthase as a
promising agent for the therapy of malignant glioma, file e4233f19-5add-2860-e053-6605fe0a460a
|
10
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The Small Molecule PPARγ Agonist GL516 Induces Feeding-Stimulatory Effects in Hypothalamus Cells Hypo-E22 and Isolated Hypothalami, file 063c54dc-32ef-4b0a-9d25-09dcf07ef18a
|
9
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|
Discovery of N-{3-[(ethanimidoylamino)methyl]benzyl}-L-prolinamide dihydrochloride:
A new potent and selective inhibitor of the inducible nitric oxide synthase as a
promising agent for the therapy of malignant glioma, file e4233f16-d09a-2860-e053-6605fe0a460a
|
8
|
|
Structural development studies of PPARs ligands based on tyrosine scaffold, file e4233f19-569d-2860-e053-6605fe0a460a
|
7
|
|
Selective Acetamidine-Based Nitric Oxide Synthase Inhibitors: Synthesis, Docking, and Biological Studies, file e4233f19-53c7-2860-e053-6605fe0a460a
|
6
|
|
Novel Phenyldiazenyl Fibrate Analogues as PPAR α/γ/δ Pan-Agonists for the Amelioration of Metabolic Syndrome, file e4233f17-83ad-2860-e053-6605fe0a460a
|
5
|
|
null, file e4233f18-ec35-2860-e053-6605fe0a460a
|
5
|
|
Synthesis and biological characterization of 3-(imidazol-1-ylmethyl)piperidine sulfonamides as aromatase inhibitors, file e4233f19-1769-2860-e053-6605fe0a460a
|
5
|
|
Synthesis and Biological Evaluation of 2-Heteroarylthioalkanoic Acid Analogues of Clofibric Acid as Peroxisome Proliferator-Activated Receptor alfa Agonists, file e4233f14-f1d9-2860-e053-6605fe0a460a
|
4
|
|
In vitro protective effects of resveratrol and stilbene alkanoic derivatives on induced oxidative stress on c2c12 and mcf7 cells, file e4233f16-61d7-2860-e053-6605fe0a460a
|
4
|
|
Design, synthesis and biological evaluation of imidazole and triazole-based carbamates as novel aromatase inhibitors, file e4233f18-31bc-2860-e053-6605fe0a460a
|
4
|
|
Synthesis and biological evaluation of gemfibrozil chiral analogs as potential PPARa agonists, file e4233f17-a7f8-2860-e053-6605fe0a460a
|
3
|
|
Synthesis, structure-activity relationships and molecular docking studies of phenyldiazenyl sulfonamides as aromatase inhibitors, file e4233f18-8530-2860-e053-6605fe0a460a
|
3
|
|
Anticancer Activity of Stilbene-Based Derivatives, file e4233f19-3cdd-2860-e053-6605fe0a460a
|
3
|
|
Different binding and recognition modes of GL479, a dual agonist of Peroxisome Proliferator-Activated Receptor α/γ, file e4233f19-5e54-2860-e053-6605fe0a460a
|
3
|
|
Synthesis, biological evaluation and docking studies of N-substituted acetamidines as selective inhibitors of inducible nitric oxide synthase, file e4233f14-f1da-2860-e053-6605fe0a460a
|
2
|
|
N-acylsulfonamides: synthetic routes and biological potential in medicinal chemistry, file e4233f17-7aa8-2860-e053-6605fe0a460a
|
2
|
|
Cytotoxic effect of a family of Peroxisome Proliferator-Activated Receptor antagonists in colorectal and pancreatic cancer cell lines, file e4233f17-8054-2860-e053-6605fe0a460a
|
2
|
|
Development of Fibrates as Important Scaffolds in Medicinal Chemistry, file e4233f17-820f-2860-e053-6605fe0a460a
|
2
|
|
Synthesis and structure-activity relationships of fibrate-based analogues inside PPARs, file e4233f17-a743-2860-e053-6605fe0a460a
|
2
|
|
Screening of NOS activity and selectivity of newly synthesized acetamidines using RP-HPLC, file e4233f19-0fd2-2860-e053-6605fe0a460a
|
2
|
|
Editorial: Targeting tumor EMT-related signaling by natural products, file 68dceeae-1da8-43bb-9acb-207a5cbb185a
|
1
|
|
Synthesis of 2-aryloxypropanoic acids analogues of clofibric acid and assignment of the absolute configuration by 1H NMR spectroscopy and DFT calculations, file e4233f14-f19c-2860-e053-6605fe0a460a
|
1
|
|
N-Substituted acetamidines and 2-methylimidazole derivatives as selective inhibitors of neuronal nitric oxide synthase, file e4233f14-fad0-2860-e053-6605fe0a460a
|
1
|
|
PPARα agonists based on stilbene and its bioisosteres: Biological evaluation and docking studies, file e4233f15-aece-2860-e053-6605fe0a460a
|
1
|
|
Synthesis of naphthyl-, quinolin- and anthracenyl analogues of clofibric acid as PPARα agonists, file e4233f15-b906-2860-e053-6605fe0a460a
|
1
|
|
Synthetic Approach to Phenylalanine-Proline, and
Tyrosine-Proline Hybrid Amino Acids, file e4233f16-8a81-2860-e053-6605fe0a460a
|
1
|
|
PPARα as Potential Therapeutic Target for Neurodegenerative Diseases, file e4233f17-1150-2860-e053-6605fe0a460a
|
1
|
|
The Selective Acetamidine-Based iNOS Inhibitor CM544 Reduces Glioma Cell Proliferation by Enhancing PARP-1 Cleavage In Vitro, file e4233f17-1c68-2860-e053-6605fe0a460a
|
1
|
|
Synthesis, characterization and evaluation of gemfibrozil-stilbene hybrid as antioxidant agent, file e4233f17-7472-2860-e053-6605fe0a460a
|
1
|
|
Fibrate-derived N-(methylsulfonyl)amides with antagonistic properties on PPARa, file e4233f17-80ad-2860-e053-6605fe0a460a
|
1
|
|
Synthesis, biological evaluation, and docking study of indole aryl sulfonamides as aromatase inhibitors, file e4233f19-1257-2860-e053-6605fe0a460a
|
1
|
| Totale |
687 |