VITA, PATRIZIA
VITA, PATRIZIA
Scuola di Scienze del Farmaco e dei Prodotti della Salute
2’-C-Methyl derivatives of tecadenoson and 2-chloro-tecadenoson with increased selectivity for human A1 adenosine receptor
2006-01-01 Cappellacci, Loredana; Franchetti, Palmarisa; Vita, Patrizia; Petrelli, Riccardo; Pasqualini, M; Costa, B; Spinetti, F; Martini, C; Klotz, K. N.; Lavecchia, A; Grifantini, Mario
3’-C-Methyl-ribosyl nucleosides as cytotoxic compounds
2005-01-01 Cappellacci, L.; Franchetti, P.; Grifantini, M.; Pasqualini, M.; Petrelli, R.; Vita, P.; Jayaram, H.; Horvath, Z.; Szekeres, T.
5'-Chloro-5'-deoxy-N6-(±)-endo-norbornyladenosine, a potent and highly selective human A1 adenosine receptor agonist modulates neuropathic pain in mice.
2009-01-01 Livio, Luongo; Cappellacci, Loredana; Enza, Palazzo; Claudia, Rossi; Vita, Patrizia; Petrelli, Riccardo; Grifantini, Mario; Sabatino, Maione
5'-CHLORO-5'-DEOXY-N6-(±)-endo-NORBORNYLADENOSINE, A POTENT AND HIGHLY SELECTIVE HUMAN A1 ADENOSINE RECEPTOR AGONIST, PREVENTS HYPERALGESIA/ALLODYNIA AND EARLY OVER-EXPRESSION OF PRO-APOPTOTIC AND PRO-INFLAMMATORY GENES IN A MICE MODEL OF NEUROPATHIC PAIN
2010-01-01 V., De Novellis; Cappellacci, Loredana; L., Luongo; Vita, Patrizia; Petrelli, Riccardo; Grifantini, Mario; S., Maione
5’-CHLORO-5’-DEOXY-N6-SUBSTITUTED ADENOSINE DERIVATIVES: SYNTHESIS, ADENOSINE RECEPTOR AFFINITY AND ANTINOCICEPTIVE ACTIVITY
2013-01-01 Petrelli, Riccardo; Torquati, Ilaria; Vita, Patrizia; L., Luongo; K. N., Klotz; S., Kachler; F., Guida; M., De Chiaro; S., Maione; Franchetti, Palmarisa; Grifantini, Mario; Cappellacci, Loredana
5’-deoxy-5’-N-pyrazolyl-N6-substituded adenosine derivates as A1 adenosine receptor agonists: synthesis and antinociception in mice
2015-01-01 Petrelli, Riccardo; Torquati, Ilaria; Livio, Luongo; Sonja, Kachler; Vita, Patrizia; Scortichini, Mirko; Antonio, Lavecchia; Sabatino, Maione; Karl Nornert, Klotz; Cappellacci, Loredana
ADP- and ATP-mimetics derived from 2'(3')-C-methyladenosine as human P2Y1 and P2Y2 receptor ligands
2012-01-01 Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Torquati, Ilaria; Jacobson, Ka; Barrett, Mo; Franklin, D; Harden, Kt; Franchetti, Palmarisa; Grifantini, Mario
ADP-, and ATP-mimetics derived from 2'(3')-C-methyladenosine as human P2Y1 and P2Y2 ligands
2011-01-01 Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Torquati, Ilaria; Kenneth A., Jacobson; Matthew, Barrett; T., Kendall Harden; Franchetti, Palmarisa; Grifantini, Mario
Affinity and selectivity of tecadenoson, 2-chloro-tecadenoson and 2’-C-methyl analogues at bovine and pig A1 adenosine receptor
2005-01-01 Cappellacci, Loredana; Franchetti, Palmarisa; Grifantini, Mario; Vita, Patrizia; Petrelli, Riccardo; Pasqualini, M.; Costa, B.; Spinetti, F.; Martini, C.; Klotz, K.; Lavecchia, A.
Antitumor effects of novel co-drugs linking histone deacetylase and ribonucleotide reductase inhibitors in hematological tumors
2011-01-01 A., Ferro; Cappellacci, Loredana; A., Mingrino; Petrelli, Riccardo; M., Tolomeo; Vita, Patrizia; N., D’Alessandro; L., Dusonchet; Franchetti, Palmarisa; Grifantini, Mario; M., Meli
ATP-mimetics derived from 2 '(3 ')-C-methyladenosine as human P2Y2 agonists
2008-01-01 Cappellacci, Loredana; Franchetti, Palmarisa; Petrelli, Riccardo; Vita, Patrizia; Jacobson, K. A.; Maddileti, S.; Harden, T. K.; Grifantini, Mario
Bisphosphonate Derivatives of 2’-C-Methyl-, and 3’-C-Methyl-Adenosine as Ligands at P2Y1 and P2Y2 Receptors
2012-01-01 Petrelli, Riccardo; Vita, Patrizia; Franchetti, P; Torquati, Ilaria; Barrett, O. M.; Harden, Kt; Grifantini, M; Cappellacci, Loredana
Design, synthesis and biological evaluation of novel inhibitors of NAD kinase
2012-01-01 Torquati, Ilaria; Vita, Patrizia; Petrelli, Riccardo; Di Stefano, M; Cappellacci, Loredana
Dual-target dimeric molecules with antitumor properties. Synthesis and biological activity of 3’-C-methyladenosine-valproates
2010-01-01 Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Franchetti, Palmarisa; Jayaram, Hn; Grifantini, Mario
EFFECTS OF METAL(III) COORDINATION ON BIOLOGICAL ACTIVITY OF 2,2'-BIPYRIDYL-6-CARBOTHIOAMIDE (BPYTA), A POTENT R2 RIBONUCLEOTIDE REDUCTASE INHIBITOR
2010-01-01 Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Grifantini, Mario; Heffeter P., Kowol CR; Franchetti, Palmarisa
First TiCl4-Mediated Diastereoslective Reduction of alpha-Nitro Ketones to beta-Nitro Alcohols by BH3.SMe2
2000-01-01 Ballini, Roberto; Bosica, Giovanna; Marcantoni, Enrico; Vita, Patrizia; Bartoli, G.
From the covalent linkage of drugs to novel inhibitors of ribonucleotide reductase: synthesis and biological evaluation of valproic esters of 3'-C-methyladenosine
2014-01-01 Petrelli, Riccardo; Maria, Meli; Vita, Patrizia; Torquati, Ilaria; Arianna, Ferro; Munender, Vodnala; Natale, D’Alessandro; Manlio, Tolomeo; DEL BELLO, Fabio; Praveen, Kusumanchi; Palmarisa, Franchetti; Mario, Grifantini; Hiremagalur N., Jayaram; Anders, Hofer; Cappellacci, Loredana
Inhibition of HIV-1 replication in macrophages by red blood cell-mediated delivery of a heterodinucleotide of lamivudine and tenofovir
2007-01-01 Franchetti, Palmarisa; Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Grifantini, Mario; Rossi, L.; Pierige', F.; Serafini, S.; Magnani, M.; Balestra, E.; Perno, C. F.
N6/5’-DISUBSTITUTED ADENOSINE AND 2-CHLORO-ADENOSINE DERIVATIVES AS POTENT AND SELECTIVE A1 ADENOSINE RECEPTOR AGONISTS: SYNTHESIS, BINDING ASSAYS AND ANTINOCICEPTIVE ACTIVITY IN MICE
2013-01-01 Petrelli, Riccardo; Vita, Patrizia; Torquati, Ilaria; L., Luongo; F., Guida; M., De Chiaro; K. N., Klotz; S., Kachler; P., Franchetti; S., Maione; M., Grifantini; Cappellacci, Loredana
N6/5’-DISUBSTITUTED ADENOSINE AND 2-CHLORO-ADENOSINE DERIVATIVES AS POTENT AND SELECTIVE A1 ADENOSINE RECEPTOR AGONISTS: SYNTHESIS, BINDING ASSAYS AND ANTINOCICEPTIVE ACTIVITY IN MICE
2014-01-01 Petrelli, Riccardo; Vita, Patrizia; Torquati, Ilaria; Livio, Luongo; Francesca, Guida; Maria De, Chiaro; Karl Norbert, Klotz; Sonja, Kachler; Palmarisa, Franchetti; Sabatino, Maione; Mario, Grifantini; Cappellacci, Loredana
| Titolo | Data di pubblicazione | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 2’-C-Methyl derivatives of tecadenoson and 2-chloro-tecadenoson with increased selectivity for human A1 adenosine receptor | 1-gen-2006 | Cappellacci, Loredana; Franchetti, Palmarisa; Vita, Patrizia; Petrelli, Riccardo; Pasqualini, M; Costa, B; Spinetti, F; Martini, C; Klotz, K. N.; Lavecchia, A; Grifantini, Mario | Poster atto convegno su rivista | |
| 3’-C-Methyl-ribosyl nucleosides as cytotoxic compounds | 1-gen-2005 | Cappellacci, L.; Franchetti, P.; Grifantini, M.; Pasqualini, M.; Petrelli, R.; Vita, P.; Jayaram, H.; Horvath, Z.; Szekeres, T. | Contributo in atto di convegno su volume | |
| 5'-Chloro-5'-deoxy-N6-(±)-endo-norbornyladenosine, a potent and highly selective human A1 adenosine receptor agonist modulates neuropathic pain in mice. | 1-gen-2009 | Livio, Luongo; Cappellacci, Loredana; Enza, Palazzo; Claudia, Rossi; Vita, Patrizia; Petrelli, Riccardo; Grifantini, Mario; Sabatino, Maione | Poster atto convegno su volume | |
| 5'-CHLORO-5'-DEOXY-N6-(±)-endo-NORBORNYLADENOSINE, A POTENT AND HIGHLY SELECTIVE HUMAN A1 ADENOSINE RECEPTOR AGONIST, PREVENTS HYPERALGESIA/ALLODYNIA AND EARLY OVER-EXPRESSION OF PRO-APOPTOTIC AND PRO-INFLAMMATORY GENES IN A MICE MODEL OF NEUROPATHIC PAIN | 1-gen-2010 | V., De Novellis; Cappellacci, Loredana; L., Luongo; Vita, Patrizia; Petrelli, Riccardo; Grifantini, Mario; S., Maione | Contributo in atto di convegno su rivista | |
| 5’-CHLORO-5’-DEOXY-N6-SUBSTITUTED ADENOSINE DERIVATIVES: SYNTHESIS, ADENOSINE RECEPTOR AFFINITY AND ANTINOCICEPTIVE ACTIVITY | 1-gen-2013 | Petrelli, Riccardo; Torquati, Ilaria; Vita, Patrizia; L., Luongo; K. N., Klotz; S., Kachler; F., Guida; M., De Chiaro; S., Maione; Franchetti, Palmarisa; Grifantini, Mario; Cappellacci, Loredana | Poster atto convegno su volume | |
| 5’-deoxy-5’-N-pyrazolyl-N6-substituded adenosine derivates as A1 adenosine receptor agonists: synthesis and antinociception in mice | 1-gen-2015 | Petrelli, Riccardo; Torquati, Ilaria; Livio, Luongo; Sonja, Kachler; Vita, Patrizia; Scortichini, Mirko; Antonio, Lavecchia; Sabatino, Maione; Karl Nornert, Klotz; Cappellacci, Loredana | Poster atto convegno su volume | |
| ADP- and ATP-mimetics derived from 2'(3')-C-methyladenosine as human P2Y1 and P2Y2 receptor ligands | 1-gen-2012 | Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Torquati, Ilaria; Jacobson, Ka; Barrett, Mo; Franklin, D; Harden, Kt; Franchetti, Palmarisa; Grifantini, Mario | Contributo in atto di convegno su rivista | |
| ADP-, and ATP-mimetics derived from 2'(3')-C-methyladenosine as human P2Y1 and P2Y2 ligands | 1-gen-2011 | Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Torquati, Ilaria; Kenneth A., Jacobson; Matthew, Barrett; T., Kendall Harden; Franchetti, Palmarisa; Grifantini, Mario | Poster atto convegno su volume | |
| Affinity and selectivity of tecadenoson, 2-chloro-tecadenoson and 2’-C-methyl analogues at bovine and pig A1 adenosine receptor | 1-gen-2005 | Cappellacci, Loredana; Franchetti, Palmarisa; Grifantini, Mario; Vita, Patrizia; Petrelli, Riccardo; Pasqualini, M.; Costa, B.; Spinetti, F.; Martini, C.; Klotz, K.; Lavecchia, A. | Poster atto convegno su volume | |
| Antitumor effects of novel co-drugs linking histone deacetylase and ribonucleotide reductase inhibitors in hematological tumors | 1-gen-2011 | A., Ferro; Cappellacci, Loredana; A., Mingrino; Petrelli, Riccardo; M., Tolomeo; Vita, Patrizia; N., D’Alessandro; L., Dusonchet; Franchetti, Palmarisa; Grifantini, Mario; M., Meli | Poster atto convegno su volume | |
| ATP-mimetics derived from 2 '(3 ')-C-methyladenosine as human P2Y2 agonists | 1-gen-2008 | Cappellacci, Loredana; Franchetti, Palmarisa; Petrelli, Riccardo; Vita, Patrizia; Jacobson, K. A.; Maddileti, S.; Harden, T. K.; Grifantini, Mario | Poster atto convegno su rivista | |
| Bisphosphonate Derivatives of 2’-C-Methyl-, and 3’-C-Methyl-Adenosine as Ligands at P2Y1 and P2Y2 Receptors | 1-gen-2012 | Petrelli, Riccardo; Vita, Patrizia; Franchetti, P; Torquati, Ilaria; Barrett, O. M.; Harden, Kt; Grifantini, M; Cappellacci, Loredana | Poster atto convegno su volume | |
| Design, synthesis and biological evaluation of novel inhibitors of NAD kinase | 1-gen-2012 | Torquati, Ilaria; Vita, Patrizia; Petrelli, Riccardo; Di Stefano, M; Cappellacci, Loredana | Contributo in atto di convegno su volume | |
| Dual-target dimeric molecules with antitumor properties. Synthesis and biological activity of 3’-C-methyladenosine-valproates | 1-gen-2010 | Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Franchetti, Palmarisa; Jayaram, Hn; Grifantini, Mario | Poster atto convegno su volume | |
| EFFECTS OF METAL(III) COORDINATION ON BIOLOGICAL ACTIVITY OF 2,2'-BIPYRIDYL-6-CARBOTHIOAMIDE (BPYTA), A POTENT R2 RIBONUCLEOTIDE REDUCTASE INHIBITOR | 1-gen-2010 | Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Grifantini, Mario; Heffeter P., Kowol CR; Franchetti, Palmarisa | Poster atto convegno su volume | |
| First TiCl4-Mediated Diastereoslective Reduction of alpha-Nitro Ketones to beta-Nitro Alcohols by BH3.SMe2 | 1-gen-2000 | Ballini, Roberto; Bosica, Giovanna; Marcantoni, Enrico; Vita, Patrizia; Bartoli, G. | Articolo | |
| From the covalent linkage of drugs to novel inhibitors of ribonucleotide reductase: synthesis and biological evaluation of valproic esters of 3'-C-methyladenosine | 1-gen-2014 | Petrelli, Riccardo; Maria, Meli; Vita, Patrizia; Torquati, Ilaria; Arianna, Ferro; Munender, Vodnala; Natale, D’Alessandro; Manlio, Tolomeo; DEL BELLO, Fabio; Praveen, Kusumanchi; Palmarisa, Franchetti; Mario, Grifantini; Hiremagalur N., Jayaram; Anders, Hofer; Cappellacci, Loredana | Articolo | |
| Inhibition of HIV-1 replication in macrophages by red blood cell-mediated delivery of a heterodinucleotide of lamivudine and tenofovir | 1-gen-2007 | Franchetti, Palmarisa; Cappellacci, Loredana; Petrelli, Riccardo; Vita, Patrizia; Grifantini, Mario; Rossi, L.; Pierige', F.; Serafini, S.; Magnani, M.; Balestra, E.; Perno, C. F. | Articolo | |
| N6/5’-DISUBSTITUTED ADENOSINE AND 2-CHLORO-ADENOSINE DERIVATIVES AS POTENT AND SELECTIVE A1 ADENOSINE RECEPTOR AGONISTS: SYNTHESIS, BINDING ASSAYS AND ANTINOCICEPTIVE ACTIVITY IN MICE | 1-gen-2013 | Petrelli, Riccardo; Vita, Patrizia; Torquati, Ilaria; L., Luongo; F., Guida; M., De Chiaro; K. N., Klotz; S., Kachler; P., Franchetti; S., Maione; M., Grifantini; Cappellacci, Loredana | Poster atto convegno su volume | |
| N6/5’-DISUBSTITUTED ADENOSINE AND 2-CHLORO-ADENOSINE DERIVATIVES AS POTENT AND SELECTIVE A1 ADENOSINE RECEPTOR AGONISTS: SYNTHESIS, BINDING ASSAYS AND ANTINOCICEPTIVE ACTIVITY IN MICE | 1-gen-2014 | Petrelli, Riccardo; Vita, Patrizia; Torquati, Ilaria; Livio, Luongo; Francesca, Guida; Maria De, Chiaro; Karl Norbert, Klotz; Sonja, Kachler; Palmarisa, Franchetti; Sabatino, Maione; Mario, Grifantini; Cappellacci, Loredana | Poster atto convegno su rivista |