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Acta Crystallographica. Section D, Biological Crystallography|July 10, 2014
Structural basis of the transactivation deficiency of the human PPARγ F360L mutant associated with familial partial lipodystrophyClorinda Lori, Alessandra Pasquo, Roberta Montanari, et al.
Journal of Medicinal Chemistry|September 11, 2018
Identification of the First PPARα/γ Dual Agonist Able To Bind to Canonical and Alternative Sites of PPARγ and To Inhibit Its Cdk5-Mediated PhosphorylationAntonio Laghezza, Luca Piemontese, Carmen Cerchia, et al.
European Journal of Medicinal Chemistry|December 13, 2021
Development of novel phenoxyalkylpiperidines as high-affinity Sigma-1 (σ1) receptor ligands with potent anti-amnesic effectFrancesca S Abatematteo, Philip D Mosier, Mauro Niso, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 27, 2011
Structural nucleotide analogs are potent activators/inhibitors of pancreatic β cell KATP channels: an emerging mechanism supporting their use as antidiabetic drugsDomenico Tricarico, Jean-François Rolland, Gianluigi Cannone, et al.
Scientific Reports|July 20, 2017
Betulinic acid is a PPARγ antagonist that improves glucose uptake, promotes osteogenesis and inhibits adipogenesisGloria Brusotti, Roberta Montanari, Davide Capelli, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 25, 2016
Catechol-based matrix metalloproteinase inhibitors with additional antioxidative activityMarilena Tauro, Antonio Laghezza, Fulvio Loiodice, et al.
Biomolecules|January 20, 2021
Derivatives of Tenuazonic Acid as Potential New Multi-Target Anti-Alzheimer's Disease AgentsViviana Poliseno, Sílvia Chaves, Leonardo Brunetti, et al.
Pharmaceuticals (Basel, Switzerland)|June 5, 2020
Bone-Seeking Matrix Metalloproteinase Inhibitors for the Treatment of Skeletal MalignancyAntonio Laghezza, Luca Piemontese, Leonardo Brunetti, et al.
Journal of Medicinal Chemistry|August 19, 2005
Synthesis, biological evaluation, and molecular modeling investigation of new chiral fibrates with PPARalpha and PPARgamma agonist activityAlessandra Pinelli, Cristina Godio, Antonio Laghezza, et al.
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