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Chemistry & Biodiversity|January 22, 2008
Synthesis and stability in biological media of 1H-imidazole-1-carboxylates of ROS203, an antagonist of the histamine H3 receptorMirko Rivara, Federica Vacondio, Claudia Silva, et al.International Journal of Pharmaceutics|September 12, 2024
Investigating drug-gut microbiota interactions: reductive and hydrolytic metabolism of oral glucocorticoids by in vitro artificial gut microbiotaMartina Viglioli, Sonia Mirjam Rizzo, Giulia Alessandri, et al.Bioorganic & Medicinal Chemistry Letters|May 23, 2006
Dibasic non-imidazole histamine H3 receptor antagonists with a rigid biphenyl scaffoldGiovanni Morini, Mara Comini, Mirko Rivara, et al.Bioorganic & Medicinal Chemistry|November 3, 2005
Synthesis and biological evaluation of new non-imidazole H3-receptor antagonists of the 2-aminobenzimidazole seriesMirko Rivara, Valentina Zuliani, Giuseppe Cocconcelli, et al.Bioorganic & Medicinal Chemistry|November 4, 2008
Synthesis and structure-activity relationships for biphenyl H3 receptor antagonists with moderate anti-cholinesterase activityGiovanni Morini, Mara Comini, Mirko Rivara, et al.Journal of Chemical Information and Modeling|October 8, 2014
Combining ligand- and structure-based approaches for the discovery of new inhibitors of the EPHA2-ephrin-A1 interactionDaniele Pala, Riccardo Castelli, Matteo Incerti, et al.Advances in Experimental Medicine and Biology|June 23, 2004
Antioxidant and cytoprotective activity of indole derivatives related to melatoninMarco Mor, Gilberto Spadoni, Giuseppe Diamantini, et al.Chemmedchem|June 26, 2009
Structure-property relationships of a class of carbamate-based fatty acid amide hydrolase (FAAH) inhibitors: chemical and biological stabilityFederica Vacondio, Claudia Silva, Alessio Lodola, et al.Journal of Medicinal Chemistry|April 4, 2003
Three-dimensional quantitative structure-activity relationship studies on selected MT1 and MT2 melatonin receptor ligands: requirements for subtype selectivity and intrinsic activity modulationSilvia Rivara, Marco Mor, Claudia Silva, et al.European Journal of Medicinal Chemistry|August 9, 2011
Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: steric effects of N-alkyl chain on rat plasma and liver stabilityFederica Vacondio, Claudia Silva, Alessio Lodola, et al.Pageof 20