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CIGNARELLA, GIORGIO

CIGNARELLA, GIORGIO  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 78 (tempo di esecuzione: 0.014 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Synthesis, modelling and antimitotic properties of tricyclic systems characterized by 2-(5-phenyl-1H-pyrrol-3-yl)-1,3,4-oxadiazole moiety 2009 S. VillaG. Cignarella + Conference Object -
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. CappellettiR. ArtaliG. CignarellaL.P. SolanoS. Villa + Article (author) -
Synthesis, molecular modelling and cytotoxicity of new 1,3,4-oxadiazoles derivatives with antimitotic activity 2008 S. VillaR. ArtaliG. Cignarella + Conference Object -
Synthesis and biological activity of new antiviral compounds 2007 L. SolanoG. CignarellaS. Villa Conference Object -
3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-1H-benzo[g]indole and related compounds : synthesis and cytotoxic activities 2006 S. VillaSOLANO, LUCREZIA PAOLAG. Cignarella + Conference Object -
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for the opioid receptors 2006 S. VillaG. Cignarella + Article (author) -
Synthesis and cytotoxic activities of 3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-1H-benzo[g]indole and related compounds 2005 S. VillaL. SolanoG. Cignarella + Article (author) -
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for the opioids receptors 2005 S. VillaG. Cignarella. G.A. Pinna + Article (author) -
Pyridazine derivatives as novel acyl-CoA:cholesterol acyltransferase (ACAT) inhibitors 2004 A. GelainD. BarloccoG. Cignarella + Conference Object -
Sintesi, attività e modelling di derivati mono- e difenilpiridazinici come potenziali inibitori dell'enzima acil-CoA colesterolo aciltrasferasi (ACAT) 2004 A. GelainD. BarloccoG. Cignarella + Conference Object -
Sintesi e valutazione farmacologia di nuovi ligandi per il recettore dell’acido gamma-idrossi butirrico 2004 S. VillaG. Cignarella + Conference Object -
Synthesis, screening, and molecular modeling of new potent and selective antagonists at the alpha 1d adrenergic receptor 2004 D. BarloccoG. Cignarella + Article (author) -
Pharmacokinetics and distribution of sodium 3,4-diaminonaphtalene-1-sulfonate, a Congo Red derivative active in inhibiting PrPres replication 2004 M. GervasoniC. PolleraS. VillaG. CignarellaG. PoliS.R. Bareggi + Article (author) -
Congo red analogues as potential anti-prion agents 2003 S. VillaG. CignarellaD. Barlocco + Article (author) -
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 Cignarella G.Villa S. + Article (author) -
6-Chloropyridazin-3-yl-derivatives active as nicotinic agents: synthesis, binding, and modeling studies 2002 G. CignarellaA. GelainD. Barlocco + Article (author) -
Versatility of the pyridazine system: Chemistry and biology 2002 G. CignarellaD. Barlocco Article (author) -
Phenylpiperazinylalkylamino substituted pyridazinones as potent alpha1 adrenoceptor antagonists 2001 D. BarloccoG. Cignarella + Article (author) -
3,8-diazabicyclo[3.2.1]octane derivatives as analogues of abasilide, a class III antiarrhythmic agent 2001 S. VillaD. BarloccoG. Cignarella + Article (author) -
Non peptidic ligands at the opioid receptor like-1 (ORL-1) 2001 D. BarloccoG. Cignarella + Article (author) -