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Journal of Pineal Research|February 14, 2004
Indole-based analogs of melatonin: in vitro antioxidant and cytoprotective activitiesMarco Mor, Claudia Silva, Federica Vacondio, et al.Journal of Medicinal Chemistry|June 17, 2016
Fatty Acid Amide Hydrolase (FAAH), Acetylcholinesterase (AChE), and Butyrylcholinesterase (BuChE): Networked Targets for the Development of Carbamates as Potential Anti-Alzheimer's Disease AgentsSerena Montanari, Laura Scalvini, Manuela Bartolini, et al.Journal of Medicinal Chemistry|December 7, 2007
N-(substituted-anilinoethyl)amides: design, synthesis, and pharmacological characterization of a new class of melatonin receptor ligandsSilvia Rivara, Alessio Lodola, Marco Mor, et al.Journal of Medicinal Chemistry|January 4, 2013
Synthesis of (E)-8-(3-chlorostyryl)caffeine analogues leading to 9-deazaxanthine derivatives as dual A(2A) antagonists/MAO-B inhibitorsSilvia Rivara, Giovanni Piersanti, Francesca Bartoccini, et al.Journal of Pineal Research|April 12, 2024
Binding and unbinding of potent melatonin receptor ligands: Mechanistic simulations and experimental evidenceAnnalida Bedini, Gian Marco Elisi, Fabiola Fanini, et al.European Journal of Medicinal Chemistry|April 26, 2014
Towards the development of 5-HT₇ ligands combining serotonin-like and arylpiperazine moietiesGilberto Spadoni, Annalida Bedini, Silvia Bartolucci, et al.Journal of Medicinal Chemistry|May 30, 2008
Synthesis and quantitative structure-activity relationship of fatty acid amide hydrolase inhibitors: modulation at the N-portion of biphenyl-3-yl alkylcarbamatesMarco Mor, Alessio Lodola, Silvia Rivara, et al.Chemsuschem|April 27, 2021
Palladium Catalyst Recycling for Heck-Cassar-Sonogashira Cross-Coupling Reactions in Green Solvent/Base BlendTommaso Fantoni, Sara Bernardoni, Alexia Mattellone, et al.Molecular Cancer Therapeutics|February 19, 2008
Dual mechanisms of action of the 5-benzylidene-hydantoin UPR1024 on lung cancer cell linesAndrea Cavazzoni, Roberta R Alfieri, Caterina Carmi, et al.Bioorganic & Medicinal Chemistry|February 5, 2004
Synthesis, biological activity, QSAR and QSPR study of 2-aminobenzimidazole derivatives as potent H3-antagonistsMarco Mor, Fabrizio Bordi, Claudia Silva, et al.Pageof 20