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Journal of Medicinal Chemistry|October 1, 2004
Cyclohexylcarbamic acid 3'- or 4'-substituted biphenyl-3-yl esters as fatty acid amide hydrolase inhibitors: synthesis, quantitative structure-activity relationships, and molecular modeling studiesMarco Mor, Silvia Rivara, Alessio Lodola, et al.Molecules (Basel, Switzerland)|September 9, 2020
Chiral Recognition of Flexible Melatonin Receptor Ligands Induced by Conformational EquilibriaGian Marco Elisi, Annalida Bedini, Laura Scalvini, et al.Journal of Medicinal Chemistry|January 13, 2016
Investigations on the 4-Quinolone-3-carboxylic Acid Motif. 7. Synthesis and Pharmacological Evaluation of 4-Quinolone-3-carboxamides and 4-Hydroxy-2-quinolone-3-carboxamides as High Affinity Cannabinoid Receptor 2 (CB2R) Ligands with Improved Aqueous SolubilityClaudia Mugnaini, Antonella Brizzi, Alessia Ligresti, et al.Chemistry & Biology|October 31, 2009
Discovery of potent and reversible monoacylglycerol lipase inhibitorsAlvin R King, Emmanuel Y Dotsey, Alessio Lodola, et al.The Journal of Physical Chemistry. B|May 10, 2013
Nonempirical energetic analysis of reactivity and covalent inhibition of fatty acid amide hydrolaseEwa I Chudyk, Edyta Dyguda-Kazimierowicz, Karol M Langner, et al.Progress in Neuro-Psychopharmacology & Biological Psychiatry|July 14, 2012
Anxiolytic effects of the melatonin MT(2) receptor partial agonist UCM765: comparison with melatonin and diazepamRafael Ochoa-Sanchez, Quentin Rainer, Stefano Comai, et al.Bioorganic & Medicinal Chemistry|August 9, 2005
Validation of a histamine H3 receptor model through structure-activity relationships for classical H3 antagonistsSimone Lorenzi, Marco Mor, Fabrizio Bordi, et al.Bioorganic & Medicinal Chemistry|January 25, 2006
Reassessing the melatonin pharmacophore--enantiomeric resolution, pharmacological activity, structure analysis, and molecular modeling of a constrained chiral melatonin analogueSilvia Rivara, Giuseppe Diamantini, Barbara Di Giacomo, et al.Scientific Reports|December 15, 2015
Cardioprotective effects of fatty acid amide hydrolase inhibitor URB694, in a rodent model of trait anxietyLuca Carnevali, Federica Vacondio, Stefano Rossi, et al.Journal of Medicinal Chemistry|May 30, 2003
Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitorsGiorgio Tarzia, Andrea Duranti, Andrea Tontini, et al.Pageof 20