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International Journal of Molecular Sciences|September 16, 2014
Synthesis and characterization of new bivalent agents as melatonin- and histamine H3-ligandsDaniele Pala, Laura Scalvini, Alessio Lodola, et al.Journal of Medicinal Chemistry|April 21, 2012
N-(2-oxo-3-oxetanyl)carbamic acid esters as N-acylethanolamine acid amidase inhibitors: synthesis and structure-activity and structure-property relationshipsAndrea Duranti, Andrea Tontini, Francesca Antonietti, et al.Chemical Communications (Cambridge, England)|November 17, 2017
Synthesis and characterization of the first inhibitor of N-acylphosphatidylethanolamine phospholipase D (NAPE-PLD)Beatrice Castellani, Eleonora Diamanti, Daniela Pizzirani, et al.Journal of Medicinal Chemistry|November 4, 2011
Toward the definition of stereochemical requirements for MT2-selective antagonists and partial agonists by studying 4-phenyl-2-propionamidotetralin derivativesAnnalida Bedini, Simone Lucarini, Gilberto Spadoni, et al.European Journal of Medicinal Chemistry|May 3, 2016
Combined inhibition of the EGFR/AKT pathways by a novel conjugate of quinazoline with isothiocyanateAndrea Tarozzi, Chiara Marchetti, Benedetta Nicolini, et al.Plos One|June 9, 2015
Amino Acid Derivatives as Palmitoylethanolamide Prodrugs: Synthesis, In Vitro Metabolism and In Vivo Plasma Profile in RatsFederica Vacondio, Michele Bassi, Claudia Silva, et al.Chemmedchem|October 2, 2007
Synthesis, enantiomeric resolution, and structure-activity relationship study of a series of 10,11-dihydro-5H-dibenzo[a,d]cycloheptene MT2 receptor antagonistsGilberto Spadoni, Annalida Bedini, Giuseppe Diamantini, et al.The Journal of Pharmacology and Experimental Therapeutics|April 7, 2007
The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3'-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in miceRoberto Russo, Jesse Loverme, Giovanna La Rana, et al.Progress in Neuro-Psychopharmacology & Biological Psychiatry|February 14, 2024
Social stress-induced depressive-like symptoms and changes in gut microbial and lipidomic profiles are prevented by pharmacological inhibition of FAAH activity in male ratsMargherita Barbetti, Leonardo Mancabelli, Federica Vacondio, et al.Journal of Pineal Research|February 28, 2006
Synthesis, antioxidant activity and structure-activity relationships for a new series of 2-(N-acylaminoethyl)indoles with melatonin-like cytoprotective activityGilberto Spadoni, Giuseppe Diamantini, Annalida Bedini, et al.Pageof 20