QUADRI, MARTA
QUADRI, MARTA
Dipartimento di Scienze Farmaceutiche
Design, synthesis, and electrophysiological evaluation of NS6740 derivatives: Exploration of the structure-activity relationship for alpha7 nicotinic acetylcholine receptor silent activation
2020 M.C. Pismataro, N.A. Horenstein, C. Stokes, M. Quadri, M. De Amici, R.L. Papke, C. Dallanoce
Novel 5-(quinuclidin-3-ylmethyl)-1,2,4-oxadiazoles to investigate the activation of the α7 nicotinic acetylcholine receptor subtype: Synthesis and electrophysiological evaluation
2018 M. Quadri, A. Silnovic, C. Matera, N.A. Horenstein, C. Stokes, M. De Amici, R.L. Papke, C. Dallanoce
Identification of α7 Nicotinic Acetylcholine Receptor Silent Agonists Based on the Spirocyclic Quinuclidine-Δ2-Isoxazoline Scaffold : Synthesis and Electrophysiological Evaluation
2017 M. Quadri, C. Matera, A. Silnovic, M.C. Pismataro, N.A. Horenstein, C. Stokes, R.L. Papke, C. Dallanoce
Novel quinuclidine derivatives to investigate the alpha-7 nicotinic acetylcholine receptor activation: new insight and perspectives
2016 M. Quadri, C. Matera, A. Silnovic, M.C. Pismataro, N.A. Horenstein, R.L. Papke, C. Dallanoce
Modification of the anabaseine pyridine nucleus allows achieving binding and functional selectivity for the α3β4 nicotinic acetylcholine receptor subtype [Modification of the anabaseine pyridine nucleus allows achieving binding and functional selectivity for the alpha 3 beta 4 nicotinic acetylcholine receptor subtype]
2016 C. Matera, M. Quadri, M. Sciaccaluga, D.Y. Pomè, F. Fasoli, M. De Amici, S. Fucile, C. Gotti, C. Dallanoce, G. Grazioso
INVESTIGATION OF THE ROLE OF ALPHA7 NICOTINIC ACETYLCHOLINE RECEPTORS IN INFLAMMATORY DISEASES THROUGH THE DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW HETEROCYCLIC DERIVATIVES
2015 M. Quadri
Determination of acid dissociation constants of poorly water-soluble nicotinic ligands by means of electrophoretic and potentiometric techniques
2015 G. Roda, C. Dallanoce, V. Gambaro, G. Grazioso, V. Liberti, C. Matera, M. Quadri, M. De Amici
Design and synthesis of selective ligands targeting different nAChR subtypes
2014 M. Quadri, C. Matera, G. Grazioso, M. De Amici, C. Dallanoce
Dualsteric activation of M2 muscarinic acetylcholine receptors inhibits cell proliferation in human glioblastoma cell lines
2014 C. Matera, M. De Amici, M. Quadri, M. Di Bari, I. Cristofaro, A.M. Tata, C. Dallanoce
Novel pharmacological tools which activate mAChRs: a question of "dualsterism"
2014 C. Matera, C. Dallanoce, M. Quadri, U. Holzgrabe, E. Barocelli, K. Mohr, M. De Amici
Bis(ammonio)alkane-type agonists of muscarinic acetylcholine receptors: Synthesis, in vitro functional characterization, and in vivo evaluation of their analgesic activity
2014 C. Matera, L. Flammini, M. Quadri, V. Vivo, V. Ballabeni, U. Holzgrabe, K. Mohr, M. De Amici, E. Barocelli, S. Bertoni, C. Dallanoce
A convenient synthesis of 4-(2-hydroxyethyl)indolin-2-one, a useful intermediate for the preparation of both dopamine receptor agonists and protein kinase inhibitors
2014 C. Matera, M. Quadri, S. Pelucchi, M. De Amici, C. Dallanoce
Analgesic effects mediated by muscarinic ligands acting at both orthosteric and allosteric receptor binding sites
2012 C. Dallanoce, L. Flammini, C. Matera, M. Quadri, V. Ballabeni, E. Barocelli, M. De Amici