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Archiv Der Pharmazie|June 12, 2009
Parallel synthesis of O-phenoxyethyl and O-adamantyl N-acyl thiocarbamates endowed with antiproliferative activityAndrea Spallarossa, Sara Cesarini, Silvia Schenone, et al.Journal of Molecular Modeling|October 8, 2009
CoMFA and CoMSIA analyses on 4-oxo-1,4-dihydroquinoline and 4-oxo-1,4-dihydro-1,5-, -1,6- and -1,8-naphthyridine derivatives as selective CB2 receptor agonistsElena Cichero, Sara Cesarini, Luisa Mosti, et al.Acta Crystallographica. Section C, Crystal Structure Communications|June 10, 2006
A novel potent non-nucleoside reverse transcriptase inhibitor acylthiocarbamate derivative with extensive intramolecular pi-pi interactionsAngelo Mugnoli, Alberto Borassi, Andrea Spallarossa, et al.Journal of Molecular Modeling|February 23, 2010
CoMFA and CoMSIA analyses on 1,2,3,4-tetrahydropyrrolo[3,4-b]indole and benzimidazole derivatives as selective CB2 receptor agonistsElena Cichero, Sara Cesarini, Luisa Mosti, et al.Journal of Molecular Modeling|January 21, 2009
Acylthiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking studies and ligand-based CoMFA and CoMSIA analysesElena Cichero, Sara Cesarini, Andrea Spallarossa, et al.European Journal of Medicinal Chemistry|December 3, 2008
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking-based CoMFA and CoMSIA analysesElena Cichero, Sara Cesarini, Paola Fossa, et al.Journal of Molecular Modeling|December 11, 2008
Computational studies of the binding mode and 3D-QSAR analyses of symmetric formimidoester disulfides: a new class of non-nucleoside HIV-1 reverse transcriptase inhibitorElena Cichero, Sara Cesarini, Andrea Spallarossa, et al.Biochemical and Biophysical Research Communications|November 24, 2007
Crystal structures of HIV-1 reverse transcriptase complexes with thiocarbamate non-nucleoside inhibitorsAndrea Spallarossa, Sara Cesarini, Angelo Ranise, et al.Bioorganic & Medicinal Chemistry|January 30, 2008
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: Parallel synthesis, molecular modelling and structure-activity relationship studies on analogues of O-(2-phenylethyl)-N-phenylthiocarbamateSara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.Bioorganic & Medicinal Chemistry|January 30, 2008
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Parallel synthesis, molecular modelling and structure-activity relationship studies on O-[2-(hetero)arylethyl]-N-phenylthiocarbamatesSara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.Pageof 2