NACCI, VITO

NACCI, VITO  

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Titolo Data di pubblicazione Autore(i) File Abstract
'Polycondensed heterocycles. Part 12: an approach to the synthesis of 2-acetyl-1'-methyl-1,2,3,4-tetrahydrospiro[isoquinoline-1,4'-pyrrolidine]-2'-one 1-gen-2002 Gemma, Sandra; Campiani, Giuseppe; Butini, Stefania; Morelli, Elena; Minetti, Patrizia; Tinti, Ornella; Nacci, Vito -
A Comparative Molecular Field Analysis Model for 6-Arylpyrrolo[2,1-d][1,5]benzothiazepines Binding Selectively to the Mitochondrial Benzodiazepine Receptor 1-gen-1994 Greco, Giovanni; Novellino, Ettore; Fiorini, Isabella; Nacci, Vito; Campiani, Giuseppe; Ciani, Silvia M.; Garofalo, Antonio; Bernasconi, Paola; Mennini, Tiziana -
A Concerted Study Using Binding Measurements, X-ray Structural Data, and Molecular Modeling on the Stereochemical Features Responsible for the Affinity of 6-Arylpyrrolo[2,1-d][1,5]benzothiazepines toward Mitochondrial Benzodiazepine Receptors 1-gen-1995 Dalpiaz, Alessandro; Bertolasi, Valerio; Boreal, Pier Andrea; Nacci, Vito; Fiorini, Isabella; Campiani, Giuseppe; Mennini, Tiziana; Manzoni, Cristina; Novellino, Ettore; Greco, Giovanni -
A palladium-catalyzed synthetic approach to new Huperzine A analogues modified at the pyridone ring 1-gen-2003 Gemma, Sandra; Butini, Stefania; Fattorusso, Caterina; Fiorini, Isabella; Nacci, Vito; Bellebaum, Katherine; Mckissic, Down; Saxena, Ashima; Campiani, Giuseppe -
A rational approach to the design of selective substrates and potent non-transportable inhibitors of the excitatory amino acid transporter EAAC1 (EAAT3). New glutamate and aspartate analogues as potential neuroprotective agents 1-gen-2001 Campiani, G.; De Angelis, M.; Armaroli, S.; Fattorusso, C.; Catalanotti, B.; Ramunno, A.; Nacci, V.; Novellino, E.; Grewer, C.; Ionescu, D.; Rauen, T.; Griffiths, R. -
Activation of the c-Jun NH2 Terminal Kinase (JNK) Signalling Pathway is Essential During PBOX-6-Induced Apoptosis in Chronic Myelogenous leukemia (CML) Cells 1-gen-2002 MC GEE, M.; Campiani, G.; Ramunno, A.; Williams, C; Zisterer, D; Nacci, V.; Lawler, M. -
An approach to modified heterocyclic analogues of huperzine A and isohuperzine A. Synthesis of the pyrimidone and pyrazole analogues, and their anticholinesterase activity 1-gen-1996 Kozikowski, Alan P.; Campiani, Giuseppe; Nacci, Vito; Sega, Alessandro; Saxena, Ashima; Doctor, Bhupendra P. -
Antiproliferative action of pyrrolobenzoxazepine derivatives in cultured cells: Absence of correlation with binding to the peripheral-type benzodiazepine binding site 1-gen-1998 Zisterer, Daniela M.; Hance, Nicole; Campiani, Giuseppe; Garofalo, Antonio; Nacci, Vito; Williams, D. Clive -
Benzothiazine and Benzothiazepine derivatives: synthesis and preliminary biological evaluation 1-gen-1993 Garofalo, A.; Campiani, G.; Fiorini, I.; Nacci, V. -
Cardiovascular Characterization of Pyrrolo[2,1-d][1,5]benzothiazepine Derivatives Binding Selectively to the Peripheral-Type Benzodiazepine Receptor (PBR):  From Dual PBR Affinity and Calcium Antagonist Activity to Novel and Selective Calcium Entry Blockers 1-gen-1996 Campiani, Giuseppe; Fiorini, Isabella; De Filippis, Maria P.; Ciani, Silvia M.; Garofalo, Antonio; Nacci, Vito; Giorgi, Gianluca; Sega, Alessandro; Botta, Maurizio; Chiarini, Alberto; Budriesi, Roberta; Bruni, Giancarlo -
Caspase-3 is not essential for DNA fragmentation in MCF-7 cells during apoptosis induced by the pyrrolo-1,5-benzoxazepine, PBOX-6 1-gen-2002 Mc Gee, Margaret M.; Hyland, Edel; Campiani, Giuseppe; Ramunno, Anna; Nacci, Vito; Zisterer, Daniela M. -
Characterisation of 1H-cyclopentapyrimidine-2,4(1H,3H)-dione derivative (S)-CPW399 as a novel, potent and subtype-selective AMPA receptor full agonist with partial desensitization properties 1-gen-2001 Campiani, G.; Morelli, E.; Nacci, V.; Fattorusso, C.; Ramunno, A.; Novellino, E.; Greenwood, J.; Liljefors, T.; Griffiths, R.; Sinclair, C.; Reavy, H.; Kristensen, A. S.; Pickering, D. S.; Schousboe, A.; Cagnotto, A.; Fumagalli, E.; Mennini, T. -
Clotrimazole Scaffold as an Innovative Pharmacophore Towards Potent Antimalarial Agents: Design, Synthesis, Biological and Structure-Activity Relationship Studies. 1-gen-2008 Gemma, Sandra; Campiani, Giuseppe; Butini, Stefania; G., Kukreja; SANNA COCCONE, Salvatore; B., Joshi; M., Persico; Nacci, Vito; Fiorini, Isabella; E., Novellino; Fattorusso, E; O., TAGLIALATELA SCAFATI; Savini, Luisa; D., Taramelli; N., Basilico; S., Parapini; G., Morace; V., Yardley; S., Croft; M., Coletta; S., Marini; Fattorusso, Caterina -
Combining 4-Aminoquinoline- and Clotrimazole-based Pharmacophores towards Innovative and Potent Hybrid Antimalarials. 1-gen-2009 Gemma, Sandra; Campiani, Giuseppe; Butini, Stefania; B. P., Joshi; G., Kukreja; SANNA COCCONE, Salvatore; Bernetti, Matteo; M., Persico; Nacci, Vito; Fiorini, Isabella; E., Novellino; D., Taramelli; N., Basilico; S., Parapini; V., Yardley; S., Croft; S., KELLER MAERKI; M., Rottmann; R., Brun; M., Coletta; S., Marini; G., Guiso; S., Caccia; C., Fattorusso -
Design and Synthesis of Potent Antimalarial Agents Based on Clotrimazole Scaffold: Exploring an Innovative Pharmacophore. 1-gen-2007 Gemma, Sandra; Campiani, Giuseppe; Butini, Stefania; B., Joshi; G., Kukreja; M., Persico; B., Catalanotti; E., Novellino; Fattorusso, E; Nacci, Vito; Savini, Luisa; D., Taramelli; N., Basilico; G., Morace; V., Yardley; C., Fattorusso -
Design, synthesis, and structure-activity relationship studies of 4-quinolinyl- and 9-acrydinylhydrazones as potent antimalarial agents. 1-gen-2008 C., Fattorusso; Campiani, Giuseppe; G., Kukreja; M., Persico; Butini, Stefania; Romano, MARIA PIA; Altarelli, Maria; S., Ros; Brindisi, Margherita; Savini, Luisa; E., Novellino; Nacci, Vito; E., Fattorusso; S., Parapini; N., Basilico; D., Taramelli; V., Yardley; S., Croft; M., Borriello; Gemma, Sandra -
Development of molecular probes for the identification of extra interaction sites in the mid-gorge and peripheral sites of butyrylcholinesterase (BuChE). Rational design of novel, selective, and highly potent BuChE inhibitors. 1-gen-2005 Campiani, Giuseppe; Fattorusso, C; Butini, Stefania; Gaeta, A; Agnusdei, M; Gemma, Sandra; Persico, M; Catalanotti, B; Savini, Luisa; Nacci, Vito; Novellino, E; Holloway, Hw; Greig, Nh; Belinskaya, T; Fedorko, Jm; Saxena, A. -
Discovery of a new class of potential multifunctional atypical antipsychotic agents targeting dopamine d3 and serotonin 5-HT 1A and 5-HT2A receptors: Design, synthesis, and effects on behavior 1-gen-2009 Butini, Stefania; Gemma, Sandra; Campiani, Giuseppe; Franceschini, Silvia; Trotta, Francesco; Marianna, Borriello; Nicoleta, Ceres; Sindu, Ros; SANNA COCCONE, Salvatore; Bernetti, Matteo; MERI DE, Angelis; Brindisi, Margherita; Nacci, Vito; Fiorini, Isabella; Ettore, Novellino; Alfredo, Cagnotto; Tiziana, Mennini; KARIN SANDAGER, Nielsen; JESPER TOBIAS, Andreasen; JORGEN SCHEEL, Kruger; JENS D., Mikkelsen; AND CATERINA, Fattorusso -
Discovery of Huperzine A/Tacrine Hybrids as Potent Inhibitors of Human Cholinesterases Targeting Their Mid-gorge Recognition Sites 1-gen-2006 Gemma, Sandra; Gabellieri, Emanuele; Huleatt, P.; C., Fattorusso; M., Borriello; B., Catalanotti; Butini, Stefania; M., DE ANGELIS; E., Novellino; Nacci, Vito; T., Belinskaya; Saxena, Ashima; Campiani, Giuseppe -
Exploiting Protein Fluctuations at the Active-Site Gorge of Human Cholinesterases: Further Optimization of the Design Strategy to Develop Extremely Potent Inhibitors 1-gen-2008 Butini, Stefania; Campiani, Giuseppe; M., Borriello; Gemma, Sandra; Panico, Alessandro; M., Persico; B., Catalanotti; S., Ros; Brindisi, Margherita; M., Agnusdei; Fiorini, Isabella; Nacci, Vito; E., Novellino; T., Belinskaya; A., Saxena; C., Fattorusso -