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Farmaco (Societa Chimica Italiana : 1989)|September 19, 2003
Synthesis and in vitro pharmacology of novel heterocyclic muscarinic ligandsMarco De Amici, Paola Conti, Ezio Fasoli, et al.Chemmedchem|January 29, 2011
Synthesis and in vitro/in vivo evaluation of the antitrypanosomal activity of 3-bromoacivicin, a potent CTP synthetase inhibitorPaola Conti, Andrea Pinto, Pui E Wong, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 23, 2011
Engineering of α-conotoxin MII-derived peptides with increased selectivity for native α6β2* nicotinic acetylcholine receptorsLuca Pucci, Giovanni Grazioso, Clelia Dallanoce, et al.European Journal of Medicinal Chemistry|October 22, 2011
New spirocyclic Δ²-isoxazoline derivatives related to selective agonists of α7 neuronal nicotinic acetylcholine receptorsClelia Dallanoce, Fabio Frigerio, Giovanni Grazioso, et al.The Journal of Pharmacology and Experimental Therapeutics|May 3, 2008
Neuroprotective effects of the novel glutamate transporter inhibitor (-)-3-hydroxy-4,5,6,6a-tetrahydro-3aH-pyrrolo[3,4-d]-isoxazole-4-carboxylic acid, which preferentially inhibits reverse transport (glutamate release) compared with glutamate reuptakeSimona Colleoni, Anders A Jensen, Elisa Landucci, et al.Journal of Medicinal Chemistry|June 27, 2003
Synthesis and anticonvulsant activity of novel bicyclic acidic amino acidsPaola Conti, Marco De Amici, Samuele Joppolo Di Ventimiglia, et al.Chemmedchem|March 3, 2011
Design, synthesis, and pharmacological characterization of novel spirocyclic quinuclidinyl-Δ2-isoxazoline derivatives as potent and selective agonists of α7 nicotinic acetylcholine receptorsClelia Dallanoce, Pietro Magrone, Carlo Matera, et al.Journal of Medicinal Chemistry|December 23, 2016
Development of Radiolabeled Ligands Targeting the Glutamate Binding Site of the N-Methyl-d-aspartate Receptor as Potential Imaging Agents for BrainLucia Tamborini, Ying Chen, Catherine A Foss, et al.Bioorganic & Medicinal Chemistry|October 4, 2015
Development of novel dipeptide-like rhodesain inhibitors containing the 3-bromoisoxazoline warhead in a constrained conformationRoberta Ettari, Andrea Pinto, Santo Previti, et al.Chemmedchem|June 13, 2014
Synthesis and biological evaluation of papain-family cathepsin L-like cysteine protease inhibitors containing a 1,4-benzodiazepine scaffold as antiprotozoal agentsRoberta Ettari, Andrea Pinto, Lucia Tamborini, et al.Pageof 6