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Journal of Medicinal Chemistry|October 6, 2007
Structures of human monoamine oxidase B complexes with selective noncovalent inhibitors: safinamide and coumarin analogsClaudia Binda, Jin Wang, Leonardo Pisani, et al.Electrophoresis|March 24, 2009
CE can identify small molecules that selectively target soluble oligomers of amyloid beta protein and display antifibrillogenic activityRaffaella Colombo, Angelo Carotti, Marco Catto, et al.European Journal of Medicinal Chemistry|February 9, 2010
Design, synthesis and biological evaluation of indane-2-arylhydrazinylmethylene-1,3-diones and indol-2-aryldiazenylmethylene-3-ones as beta-amyloid aggregation inhibitorsMarco Catto, Rosaria Aliano, Angelo Carotti, et al.Chemmedchem|May 26, 2012
Design, synthesis, and biological evaluation of 2-aminobenzanilide derivatives as potent and selective HDAC inhibitorsDiana A Stolfa, Angela Stefanachi, Julia M Gajer, et al.Journal of Medicinal Chemistry|September 11, 2007
Solid-phase synthesis and insights into structure-activity relationships of safinamide analogues as potent and selective inhibitors of type B monoamine oxidaseFrancesco Leonetti, Carmelida Capaldi, Leonardo Pisani, et al.Journal of Medicinal Chemistry|October 13, 2006
Impact of species-dependent differences on screening, design, and development of MAO B inhibitorsLaura Novaroli, Antoine Daina, Elisabeth Favre, et al.European Journal of Medicinal Chemistry|October 7, 2004
8-Substituted-9-deazaxanthines as adenosine receptor ligands: design, synthesis and structure-affinity relationships at A2BAngelo Carotti, Angela Stefanachi, Enrique Raviña, et al.Chemistry & Biodiversity|December 29, 2006
Lipophilicity plays a major role in modulating the inhibition of monoamine oxidase B by 7-substituted coumarinsAngelo Carotti, Cosimo Altomare, Marco Catto, et al.Bioorganic & Medicinal Chemistry|April 15, 2008
Design, synthesis, and biological evaluation of glycine-based molecular tongs as inhibitors of Abeta1-40 aggregation in vitroSaverio Cellamare, Angela Stefanachi, Diana A Stolfa, et al.European Journal of Medicinal Chemistry|December 3, 2014
Discovery of new 7-substituted-4-imidazolylmethyl coumarins and 4'-substituted-2-imidazolyl acetophenones open analogues as potent and selective inhibitors of steroid-11β-hydroxylaseAngela Stefanachi, Nina Hanke, Leonardo Pisani, et al.Pageof 9