CIGNARELLA, GIORGIO
CIGNARELLA, GIORGIO
Universita' degli Studi di MILANO
Synthesis, modelling and antimitotic properties of tricyclic systems characterized by 2-(5-phenyl-1H-pyrrol-3-yl)-1,3,4-oxadiazole moiety
2009 S. Villa, G. Cignarella, E. Villa, V. Zuco, K.D. Shin, B.M. Kwon
Synthesis, Modelling, and Antimitotic Properties of Tricyclic Systems Characterised by a 2-(5-Phenyl-1H-pyrrol-3-yl)-1,3,4-oxadiazole Moiety
2009 G.A. Pinna, G. Murineddu, C. Murruzzu, V. Zuco, F. Zunino, G. Cappelletti, R. Artali, G. Cignarella, L.P. Solano, S. Villa
Synthesis, molecular modelling and cytotoxicity of new 1,3,4-oxadiazoles derivatives with antimitotic activity
2008 S. Villa, G.A. Pinna, F. Zunino, R. Artali, G. Cignarella, E. Villa
Synthesis and biological activity of new antiviral compounds
2007 L. Solano, G. Cignarella, S. Villa
3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-1H-benzo[g]indole and related compounds : synthesis and cytotoxic activities
2006 S. Villa, L.P. Solano, G. Cignarella, G. Murineddu, G.A. Pinna
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for the opioid receptors
2006 G. Loriga, I. Manca, G. Murineddu, G. Chelucci, S. Villa, S. Gessi, L. Toma, G. Cignarella, G.A. Pinna
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for the opioids receptors
2005 G. Loriga, I. Manca, G. Chelucci, S. Villa, S. Gessi, L. Toma, G. Cignarella
Synthesis and cytotoxic activities of 3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-1H-benzo[g]indole and related compounds
2005 S. Villa, L. Solano, G. Cignarella, G. Murineddu, G.A. Pinna
Pyridazine derivatives as novel acyl-CoA:cholesterol acyltransferase (ACAT) inhibitors
2004 A. Gelain, I. Bettinelli, D. Barlocco, L. Toma, B.M. Kwon, T.S. Jeong, Y.S. Kim, M.P. Giovannoni, C. Vergelli, V. Dal Piaz, G. Cignarella
Sintesi, attività e modelling di derivati mono- e difenilpiridazinici come potenziali inibitori dell'enzima acil-CoA colesterolo aciltrasferasi (ACAT)
2004 A. Gelain, I. Bettinelli, D. Barlocco, G. Cignarella, L. Toma, B.M. Kwon, T.S. Jeong, Y.S. Kim, M.P. Giovannoni, C. Vergelli, V. Dal Piaz
Synthesis, screening, and molecular modeling of new potent and selective antagonists at the alpha 1d adrenergic receptor
2004 A. Leonardi, D. Barlocco, F. Montesano, G. Cignarella, G. Motta, R. Testa, E. Poggesi, M. Seeber, P.G. De Benedetti, F. Fanelli
Sintesi e valutazione farmacologia di nuovi ligandi per il recettore dell’acido gamma-idrossi butirrico
2004 S. Villa, G. Cignarella, M.P. Castelli, G.L. Gessa
Pharmacokinetics and distribution of sodium 3,4-diaminonaphtalene-1-sulfonate, a Congo Red derivative active in inhibiting PrPres replication
2004 M. Gervasoni, R. Pirola, C. Pollera, S. Villa, G. Cignarella, P. Mantegazza, G. Poli, S.R. Bareggi
Synthesis of novel diazatricyclodecanes (DTDs). Effects of structural variation at the C3′ allyl end and at the phenyl ring of the cinnamyl chain on μ-receptor affinity and opioid antinociception
2003 G.A. Pinna, G. Cignarella, S. Ruiu, G. Loriga, G. Murineddu, S. Villa, G.E. Grella, G. Cossu, W. Fratta
Congo red analogues as potential anti-prion agents
2003 S. Villa, G. Cignarella, D. Barlocco, M. Gervasoni, G. Carcassola, L. Giannino, P. Mantegazza
Versatility of the pyridazine system: Chemistry and biology
2002 G. Cignarella, D. Barlocco
6-Chloropyridazin-3-yl-derivatives active as nicotinic agents: synthesis, binding, and modeling studies
2002 L. Toma, P. Quadrelli, W.H. Bunnelle, D.J. Anderson, M.D. Meyer, G. Cignarella, A. Gelain, D. Barlocco
Phenylpiperazinylalkylamino substituted pyridazinones as potent alpha1 adrenoceptor antagonists
2001 D. Barlocco, G. Cignarella, V. Dal Piaz, M.P. Giovannoni, P.G. De Benedetti, F. Fanelli, F. Montesano, E. Poggesi, A. Leonardi
3,8-diazabicyclo[3.2.1]octane derivatives as analogues of abasilide, a class III antiarrhythmic agent
2001 S. Villa, D. Barlocco, G. Cignarella, G.J. Papp, B. Balati, J. Takacs, A. Varrò, K. Keseru, P. Matyus
Non peptidic ligands at the opioid receptor like-1 (ORL-1)
2001 D. Barlocco, L. Toma, G. Cignarella