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European Journal of Medicinal Chemistry|May 22, 2019
An update about the crucial role of stereochemistry on the effects of Peroxisome Proliferator-Activated Receptor ligandsAntonio Laghezza, Luca Piemontese, Paolo Tortorella, et al.
Chemmedchem|July 23, 2013
Probing the S1' site for the identification of non-zinc-binding MMP-2 inhibitorsAntonella Di Pizio, Antonio Laghezza, Paolo Tortorella, et al.
Journal of Medicinal Chemistry|August 14, 2019
New Approaches to Cancer Therapy: Combining Fatty Acid Amide Hydrolase (FAAH) Inhibition with Peroxisome Proliferator-Activated Receptors (PPARs) ActivationLeonardo Brunetti, Fulvio Loiodice, Luca Piemontese, et al.
Archiv Der Pharmazie|June 23, 2011
Identification of novel matrix metalloproteinase inhibitors by screening of phenol fragments libraryMaria Teresa Rubino, Dariana Maggi, Antonio Laghezza, et al.
International Journal of Molecular Sciences|September 29, 2020
Beyond the Canonical Endocannabinoid System. A Screening of PPAR Ligands as FAAH InhibitorsLeonardo Brunetti, Antonio Carrieri, Luca Piemontese, et al.
Recent Patents on Food, Nutrition & Agriculture|March 14, 2020
A Review of Recent Patents (2016-2019) on Plant Food Supplements with Potential Application in the Treatment of Neurodegenerative and Metabolic DisordersRosalba Leuci, Leonardo Brunetti, Antonio Laghezza, et al.
Bioorganic & Medicinal Chemistry|September 28, 2013
Arylamino methylene bisphosphonate derivatives as bone seeking matrix metalloproteinase inhibitorsMarilena Tauro, Antonio Laghezza, Fulvio Loiodice, et al.
Pharmaceuticals (Basel, Switzerland)|January 27, 2021
(2-Aminobenzothiazole)-Methyl-1,1-Bisphosphonic Acids: Targeting Matrix Metalloproteinase 13 Inhibition to the BoneAntonio Laghezza, Luca Piemontese, Leonardo Brunetti, et al.
Foods (Basel, Switzerland)|December 30, 2020
Natural Compounds for the Prevention and Treatment of Cardiovascular and Neurodegenerative DiseasesRosalba Leuci, Leonardo Brunetti, Viviana Poliseno, et al.
Scientific Reports|June 11, 2016
Screening of saponins and sapogenins from Medicago species as potential PPARγ agonists and X-ray structure of the complex PPARγ/caulophyllogeninRoberta Montanari, Davide Capelli, Aldo Tava, et al.
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