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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.
Bioorganic & Medicinal Chemistry|February 21, 2012
Synthesis, biological evaluation and molecular investigation of fluorinated peroxisome proliferator-activated receptors α/γ dual agonistsGiuseppe Fracchiolla, Antonio Laghezza, Luca Piemontese, et al.
Chemmedchem|June 30, 2011
Biphenyl sulfonylamino methyl bisphosphonic acids as inhibitors of matrix metalloproteinases and bone resorptionMaria Teresa Rubino, Mariangela Agamennone, Cristina Campestre, et al.
European Journal of Medicinal Chemistry|December 3, 2014
Structural development studies of PPARs ligands based on tyrosine scaffoldBarbara De Filippis, Pasquale Linciano, Alessandra Ammazzalorso, et al.
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