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Synthesis and antibacterial activity of 2-aryl-2,5-dihydro-3(3H)-oxo-pyridazino4,3-bindole-4-carboxylic acids 1-gen-1999 Palluotto, Fausta; Carotti, Angelo; Casini, G.; Ferappi, M; Rosato, Antonio; Vitali, C.; Campagna, Francesco
Synthesis and structure-affinity relationships at the central benzodiazepine receptor of pyridazino4,3-bindoles and indeno1,2-cpyridazines 1-gen-1999 Campagna, Francesco; Palluotto, Fausta; Carotti, Angelo; Casini, G.; Genchi, G.
Benzodiazepine receptor affinities, behavioural and anticonvulsant activity of 2-aryl-2,5-dihydropyridazino[4,3-b]indol-3(3H)-ones in mice 1-gen-2000 DE SARRO, G.; Carotti, Angelo; Campagna, Francesco; Palluotto, Fausta; Mckernan, R.; Quirk, K.; Rizzo, M.; Giusti, P.; Rettore, C.; DE SARRO, A.
Synthesis and antibacterial activity of pyridazino[4,3-b]indole-4-carboxylic acids carrying different substituents at N-2 1-gen-2002 Palluotto, Fausta; Campagna, Francesco; Carotti, Angelo; Ferappi, M.; Rosato, Antonio; Vitali, C.
Synthesis.and biological evaluation of pyridazino[4,3-b]indoles and indeno[1,2-c]pyridazines as new ligands of central and peripheral benzodiazepine receptors 1-gen-2003 Campagna, Francesco; Palluotto, Fausta; Mascia, M. P.; Maciocco, E.; Marra, C.; Carotti, Angelo; Carrieri, Antonio
Synthesis and biological evaluation of pyrazoles and pyrazole-containing polycyclic derivatives as new ligands of central and peripheral benzodiazepine receptors 1-gen-2004 Campagna, Francesco; Palluotto, F.; Carotti, Angelo; Maciocco, E.
Indol-3-ylidene, pyridazino[4,3-b]indole and indeno[1,2-c]pyrazole derivatives:synthesis and biological evaluation as inhibitors of GSK-3 and CDKs 1-gen-2005 Campagna, Francesco; Aliano, R; Carotti, A; Palluotto, Fausta; Lozach, O; Meijer, L.
New N-arylmethyl derivatives of some cyclic amino acids and new peptidomimetics: synthesis and inhibition activity of insulin amyloid formation 1-gen-2005 Campagna, Francesco; Cellamare, Saverio; Aliano, R; Carotti, A; Ferappi, M.
Inhibiting Aβ1-40 in vitro aggregation by glycine-based molecular tongs: rational design and mechanistic implications 1-gen-2007 Campagna, Francesco; Cellamare, Saverio; Stefanachi, Angela; Stolfa, D. A.; Basile, T; Ferappi, M; Catto, Marco; Carotti, A.
Synthesis and Monoamine Oxidase Inhibitory Activity of new Pyridazine-, Pyrimidine and 1,2,4 Triazine containing Tryciclic derivatives 1-gen-2007 Carotti, Angelo; Catto, Marco; Leonetti, Francesco; Campagna, F.; SOTO OTERO, R.; MENDEZ ALVAREZ, E.; Thull, U.; Testa, B.; Altomare, Cosimo Damiano
Synthesis and Inhibitory Activity Towards β-Amyloid Fibril Formation of Indane and Indole Derivatives 1-gen-2008 Campagna, Francesco; Catto, Marco; Aliano, R; Carotti, A; Cellamare, Saverio; Greco, A; Palluotto, F.
1,3-Dialkyl-8-(hetero)aryl-9-OH-9-deazaxanthines as potent A2B adenosine receptor antagonists: design, synthesis, structure-affinity and structure-selectivity relationships 1-gen-2008 Stefanachi, Angela; Nicolotti, Orazio; Leonetti, Francesco; Cellamare, Saverio; Campagna, Francesco; Loza, Mi; Brea, Jm; Mazza, F; Gavuzzo, E; Carotti, Angelo
Design, synthesis, and biological evaluation of glycine-based molecular tongs as inhibitors of Aβ40 aggregation in vitro 1-gen-2008 Cellamare, Saverio; Stefanachi, Angela; Stolfa, D. A.; Basile, T; Catto, Marco; Campagna, Francesco; Sotelo, E; Acquafredda, Pasquale; Carotti, Angelo
Synthesis and biological evaluation of arylhydrazone derivatives of indoles and indolin-2-ones as b-amyloid aggregation inhibitors 1-gen-2009 Campagna, Francesco; Catto, Marco; Carotti, A; Cellamare, Saverio; Palluotto, Fausta; Purgatorio, R.
Synthesis and biological evaluation of arylhydrazone derivatives of indoles and indolin-2-ones as b-amyloid aggregation inhibitors 1-gen-2009 Campagna, F; Catto, M; Carotti, A; Cellamare, S; Palluotto, F; Purgatorio, R
Design, synthesis and biological evaluation of indane 2-arylhydrazinylmethylene-1,3-diones and indol-2-aryldiazenylmethylene-3-ones as b-amyloid aggregation inhibitors 1-gen-2010 Catto, Marco; Aliano, R; Carotti, Angelo; Cellamare, Saverio; Palluotto, Fausta; Purgatorio, R; DE STRADIS, A; Campagna, Francesco
Biophysical Characterization of Inhibition of A-beta Fibril Formation by Isatin-3-arylhydrazones 1-gen-2010 Campagna, Francesco; Purgatorio, R; Catto, Marco; Carotti, A; De, Stradisa; Palazzo, Gerardo
Targeting Monoamine Oxidases with Multipotent Ligands: An Emerging Strategy in the Search of New Drugs Against Neurodegenerative Diseases 1-gen-2011 Pisani, Leonardo; Catto, Marco; Leonetti, Francesco; Nicolotti, Orazio; Stefanachi, Angela; Campagna, Francesco; Carotti, Angelo
Synthesis and biophysical evaluation of arylhydrazono-1H-2-indolinones as beta-amyloid aggregation inhibitors 1-gen-2011 Campagna, Francesco; Catto, Marco; Purgatorio, R; Altomare, Cosimo Damiano; Carotti, Angelo; DE STRADIS, A; Palazzo, Gerardo
The exploration of 1,2,3,4,5,6-hexahydroazepino[4,3-b]indole derivatives as selective butyrylcholinesterase inhibitors 1-gen-2012 DE CANDIA, Modesto; Zaetta, G; Campagna, Francesco; Leonid, G. VOSKRESSENSKY L. G.; Altomare, Cosimo Damiano
Mostrati risultati da 1 a 20 di 26
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