28 results on '"Fiorucci, Stefano"'
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2. Structural Basis for Developing Multitarget Compounds Acting on Cysteinyl Leukotriene Receptor 1 and G-Protein-Coupled Bile Acid Receptor 1
3. Exploitation of Cholane Scaffold for the Discovery of Potent and Selective Farnesoid X Receptor (FXR) and G-Protein Coupled Bile Acid Receptor 1 (GP-BAR1) Ligands
4. Modification on Ursodeoxycholic Acid (UDCA) Scaffold. Discovery of Bile Acid Derivatives As Selective Agonists of Cell-Surface G-Protein Coupled Bile Acid Receptor 1 (GP-BAR1)
5. Bazedoxifene-Scaffold-Based Mimetics of Solomonsterols A and B as Novel Pregnane X Receptor Antagonists
6. Design, Synthesis, and Biological Evaluation of Potent Dual Agonists of Nuclear and Membrane Bile Acid Receptors
7. Binding Mechanism of the Farnesoid X Receptor Marine Antagonist Suvanine Reveals a Strategy To Forestall Drug Modulation on Nuclear Receptors. Design, Synthesis, and Biological Evaluation of Novel Ligands
8. Plakilactones from the Marine SpongePlakinastrella mamillaris. Discovery of a New Class of Marine Ligands of Peroxisome Proliferator-Activated Receptor γ
9. Conicasterol E, a Small Heterodimer Partner Sparing Farnesoid X Receptor Modulator Endowed with a Pregnane X Receptor Agonistic Activity, from the Marine Sponge Theonella swinhoei
10. Total Synthesis and Pharmacological Characterization of Solomonsterol A, a Potent Marine Pregnane-X-Receptor Agonist Endowed with Anti-Inflammatory Activity
11. Theonellasterols and Conicasterols from Theonella swinhoei. Novel Marine Natural Ligands for Human Nuclear Receptors
12. Discovery of Sulfated Sterols from Marine Invertebrates as a New Class of Marine Natural Antagonists of Farnesoid-X-Receptor
13. Solomonsterols A and B from Theonella swinhoei. The First Example of C-24 and C-23 Sulfated Sterols from a Marine Source Endowed with a PXR Agonistic Activity
14. Back Door Modulation of the Farnesoid X Receptor: Design, Synthesis, and Biological Evaluation of a Series of Side Chain Modified Chenodeoxycholic Acid Derivatives
15. Farnesoid X Receptor: From Structure to Potential Clinical Applications
16. Bile Acid Derivatives as Ligands of the Farnesoid X Receptor. Synthesis, Evaluation, and Structure−Activity Relationship of a Series of Body and Side Chain Modified Analogues of Chenodeoxycholic Acid
17. 6α-Ethyl-Chenodeoxycholic Acid (6-ECDCA), a Potent and Selective FXR Agonist Endowed with Anticholestatic Activity
18. Exploitation of Cholane Scaffoldfor the Discoveryof Potent and Selective Farnesoid X Receptor (FXR) and G-ProteinCoupled Bile Acid Receptor 1 (GP-BAR1) Ligands.
19. Modification on UrsodeoxycholicAcid (UDCA) Scaffold.Discovery of Bile Acid Derivatives As Selective Agonists of Cell-SurfaceG-Protein Coupled Bile Acid Receptor 1 (GP-BAR1).
20. Bazedoxifene-Scaffold-BasedMimetics of SolomonsterolsA and B as Novel Pregnane X Receptor Antagonists.
21. Design, Synthesis, and BiologicalEvaluation of PotentDual Agonists of Nuclear and Membrane Bile Acid Receptors.
22. BindingMechanism of the Farnesoid X Receptor Marine Antagonist Suvanine Revealsa Strategy To Forestall Drug Modulation on Nuclear Receptors. Design,Synthesis, and Biological Evaluation of Novel Ligands.
23. Plakilactones from theMarine Sponge Plakinastrellamamillaris. Discovery of a New Class of Marine Ligands ofPeroxisome Proliferator-Activated Receptor γ.
24. Design, synthesis, and biological evaluation of potent dual agonists of nuclear and membrane bile acid receptors.
25. Plakilactones from the marine sponge Plakinastrella mamillaris. Discovery of a new class of marine ligands of peroxisome proliferator-activated receptor γ.
26. Conicasterol E, a small heterodimer partner sparing farnesoid X receptor modulator endowed with a pregnane X receptor agonistic activity, from the marine sponge Theonella swinhoei.
27. Solomonsterols A and B from Theonella swinhoei. The first example of C-24 and C-23 sulfated sterols from a marine source endowed with a PXR agonistic activity.
28. Bile acid derivatives as ligands of the farnesoid X receptor. Synthesis, evaluation, and structure-activity relationship of a series of body and side chain modified analogues of chenodeoxycholic acid.
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