Uno studio sul gradimento del feedback in due corsi universitari online

Autor: Francesca Storai, Valentina Pedani

Publikováno v: EDUCATION SCIENCES AND SOCIETY. :296-308

In questo studio che prende in esame gli insegnamenti online Pianificazione e Valutazione della didattica e Attività sperimentali per la prima infanzia dell'Università Telematica degli Studi IUL, si sono analizzate le schede di valutazione compilat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::20f48a3a1cce3654a67a71c4b96eff65
https://doi.org/10.3280/ess2-2021oa12487

Synthesis and Biological Evaluation of Quinoxaline Derivatives for PET Imaging of the NMDA Receptor

Autor: Selena Milicevic Sephton, Peter T. Vetterli, Aristeidis Chiotellis, Adrienne Müller Herde, Sylvia Roscales, Roger Schibli, Simon M. Ametamey, Yves Auberson, Valentina Pedani, Stjepko Cermak

Publikováno v: Helvetica Chimica Acta. 100:e1700204

Due to the biological complexity of the N-methyl-d-aspartate receptor (NMDAR), the development of a positron emission tomography radiotracer for the imaging of NMDAR has met with limited success. Recent studies have established the presence of GluN2A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::55bc13a3fce301476e61b911b387afcc
https://doi.org/10.1002/hlca.201700204

Synthesis and pharmacological characterization of 2-(acylamino)thiophene derivatives as metabolically stable, orally effective, positive allosteric modulators of the GABAB receptor

Autor: Carla Lobina, Giancarlo Colombo, Valentina Pedani, Alberto Casti, Gian Luigi Gessa, Stefania Lamponi, Maria Paola Castelli, Claudia Mugnaini, Federico Corelli, Maurizio Solinas, Angelo Casu, Daniela Giunta, Alessandra Porcu, Massimo Valoti, Stefania Dragoni, Paola Maccioni

Publikováno v: Journal of medicinal chemistry (Online) 56 (2013): 3620–3635. doi:10.1021/jm400144w
info:cnr-pdr/source/autori:Claudia Mugnaini, Valentina Pedani, Angelo Casu, Carla Lobina, Alberto Casti, Paola Maccioni, Alessandra Porcu, Daniela Giunta, Stefania Lamponi, Maurizio Solinas, Stefania Dragoni, Massimo Valoti, Giancarlo Colombo, Maria Paola Castelli, Gian Luigi Gessa, Federico Corelli/titolo:Synthesis and Pharmacological Characterization of 2-(Acylamino)thiophene Derivatives as Metabolically Stable, Orally Effective, Positive Allosteric Modulators of the GABAB Receptor/doi:10.1021%2Fjm400144w/rivista:Journal of medicinal chemistry (Online)/anno:2013/pagina_da:3620/pagina_a:3635/intervallo_pagine:3620–3635/volume:56

Two recently reported hit compounds, COR627 and COR628, underpinned the development of a series of 2-(acylamino)thiophene derivatives. Some of these compounds displayed significant activity in vitro as positive allosteric modulators of the GABAB rece

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af7c61378e47961e694af15f6da1c0a5
https://pubmed.ncbi.nlm.nih.gov/23544432

Investigations on the 4-Quinolone-3-carboxylic Acid Motif. 4. Identification of New Potent and Selective Ligands for the Cannabinoid Type 2 Receptor with Diverse Substitution Patterns and Antihyperalgesic Effects in Mice

Autor: Alessia Ligresti, Livio Luongo, Maria De Chiaro, Serena Pasquini, Federico Corelli, Francesca Guida, Maria Frosini, Valentina Pedani, Vincenzo Di Marzo, Claudia Mugnaini, Sabatino Maione, Stefania Dragoni, Maria Cristina De Rosa

Publikováno v: Journal of medicinal chemistry 54 (2011): 5444–5453.
info:cnr-pdr/source/autori:Pasquini S, De Rosa M, Pedani V, Mugnaini C, Guida F, Luongo L, De Chiaro M, Maione S, Dragoni S, Frosini M, Ligresti A, Di Marzo V, Corelli F./titolo:Investigations on the 4-quinolone-3-carboxylic acid motif. 4. Identification of new potent and selective ligands for the cannabinoid type 2 receptor with diverse substitution patterns and antihyperalgesic effects in mice./doi:/rivista:Journal of medicinal chemistry/anno:2011/pagina_da:5444/pagina_a:5453/intervallo_pagine:5444–5453/volume:54

Experimental evidence suggests that selective CB2 receptor modulators may provide access to antihyperalgesic agents devoid of psychotropic effects. Taking advantage of previous findings on structure-activity/selectivity relationships for a class of 4

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37ca1f9329884d62325332cd8ad048a7
http://hdl.handle.net/11365/4091