Sfoglia per Titolo
Synthesis of the tritium labeled SCH 58261, a new non-xanthine A(2A) adenosine receptor antagonist
file con accesso da definire1996 Baraldi, Pier Giovanni; Cacciari, Barbara; Dionisotti, S; Egan, J; Spalluto, G; Zocchi, C.
Synthesis of thiourea-tethered C-glycosyl amino acids via isothiocyanate-amine coupling
file con accesso da definire2009 Barghash, R. F.; Massi, Alessandro; Dondoni, Alessandro
SYNTHESIS OF TRISACCHARIDE DERIVATIVES WITH THE SEQUENCE OF THE DESIALYLATED CAD BLOOD-GROUP DETERMINANT
file con accesso da definire1985 Catelani, G; Marra, Alberto; Paquet, F; Sinay, P.
Synthesis of Unsymmetrical Squaramides as Allosteric GSK-3β Inhibitors Promoting β-Catenin-Mediated Transcription of TCF/LEF in Retinal Pigment Epithelial Cells
2022 Carullo, G.; Bottoni, L.; Pasquini, S.; Papa, A.; Contri, C.; Brogi, S.; Calderone, V.; Orlandini, M.; Gemma, S.; Varani, K.; Butini, S.; Galvagni, F.; Vincenzi, F.; Campiani, G.
synthesis stability evaluation and permeability study of a zidovudine-bile acid prodrug
file con accesso da definire2011 Dalpiaz, Alessandro; Fogagnolo, Marco; Pavan, Barbara; Perrone, Daniela; I., Poppi
Synthesis, antibacterial activity and structure-activity relationships of N-(pyridin-2-yl) 3-substituted-4-diazopyrazole-5-carboxamides
file con accesso da definire1994 Baraldi, Pier Giovanni; Brigidi, P.; Garuti, L.; Recanatini, M.; Roberti, M.
Synthesis, antibacterial activity and structure-activity relationships of N-substituted 3-methyl-4-diazo-5-pyrazolecarboxamides.
file con accesso da definire1989 Baraldi, Pier Giovanni; Brigidi, P.; Casolari, Alberto; Manfredini, Stefano; Periotto, V.; Recanatini, M.; Roberti, M.; Rossi, M.
Synthesis, antibacterial activity and structure-activity relationships of N-substituted 4-diazopyrazole-5-carboxamides. 2
file con accesso da definire1991 Baraldi, Pier Giovanni; Cacciari, Barbara; Leoni, Alberto; Recanatini, Maurizio; Roberti, Marinella; Rossi, Maddalena; Manfredini, Stefano; Periotto, Vittorio; Simoni, Daniele
Synthesis, Antimitotic and Antivascular Activity of 1-(3’,4’,5’-Trimethoxybenzoyl)-3-Arylamino-5-Amino-1,2,4-Triazoles
file con accesso da definire2014 Romagnoli, Romeo; Baraldi, Pier Giovanni; Kimatrai Salvador, M.; Prencipe, Filippo; Bertolasi, Valerio; Cancellieri, M.; Brancale, A.; Hamel, E.; Castagliuolo, I.; Consolaro, F.; Porcù, E.; Basso, G.; Viola, G.
Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications
file con accesso da definire2012 Baldisserotto, Anna; Malisardi, Gemma; Scalambra, Emanuela; Andreotti, Elisa; C., Romagnoli; Vicentini, Chiara Beatrice; Manfredini, Stefano; Vertuani, Silvia
Synthesis, antiviral and antiproliferative activity of a new class of 5-(alkyl or arylthio)-6-vinyl uracils
file con accesso da definire1996 Baraldi, Pier Giovanni; Cacciari, Barbara; Romagnoli, Romeo; Spalluto, G; Garuti, L; Roberti, M; Pani, A; Perra, G; Scintu, F; Pinna, N; Musiu, C; Lacolla, P.
Synthesis, binding and thermodynamic studies of new highly selective A2A adenosine receptor antagonists
file con accesso da definire1997 Cacciari, Barbara; Baraldi, Pier Giovanni; Spalluto, Giampiero; Ongini, E.; Dionisotti, S.; Varani, Katia; Gessi, Stefania; Borea, Pier Andrea
Synthesis, Biological Activity and Molecular Docking of Chimeric Peptides Targeting Opioid and NOP Receptors
2022 Wtorek, Karol; Ghidini, Alessia; Gentilucci, Luca; Adamska-Bartłomiejczyk, Anna; Piekielna-Ciesielska, Justyna; Ruzza, Chiara; Sturaro, Chiara; Calò, Girolamo; Pieretti, Stefano; Kluczyk, Alicja; Mcdonald, John; Lambert, David G; Janecka, Anna
Synthesis, biological activity and molecular modeling studies of 1,2,3,4-tetrahydroisoquinoline derivatives as conformationally constrained analogues of KN62, a potent antagonist of the P2X(7)-receptor containing a tyrosine moiety
file con accesso da definire2002 Baraldi, Pier Giovanni; Makaeva, R; Pavani, Maria Giovanna; Nunez, Md; Spalluto, G; Moro, S; Falzoni, S; DI VIRGILIO, Francesco; Romagnoli, Romeo
Synthesis, biological activity, and molecular modeling investigation of new pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as human A(3) adenosine receptor antagonists
file con accesso da definire2002 Baraldi, Pier Giovanni; Cacciari, Barbara; Moro, S; Spalluto, G; Pastorin, G; DA ROS, T; Klotz, Kn; Varani, Katia; Gessi, Stefania; Borea, Pier Andrea
Synthesis, biological and modeling studies of new water soluble hA3 adenosine receptor antagonists.
file con accesso da definire2005 Pastorin, G.; Da Ros, T.; Bolcato, C.; Montopoli, C.; Moro, S.; Cacciari, Barbara; Baraldi, Pier Giovanni; Varani, Katia; Borea, Pier Andrea; Spalluto, G.
Synthesis, biological evaluation and docking studies of a novel class of sulfur-bridged diazabicyclo[3.3.1]nonanes
2020 Murineddu, Gabriele; Asproni, Battistina; Corona, Paola; Gessi, Stefania; Merighi, Stefania; Battistello, Enrica; Sturaro, Chiara; Calo', Girolamo; Galeotti, Nicoletta; Temml, Veronika; Herdlinger, Sonja; Schuster, Daniela; Pinna, Gerard A.
Synthesis, biological evaluation and structural analysis of novel peripherally active morphiceptin analogs
file con accesso da definire2016 Adamska, Anna; Kluczyk, Alicja; Cerlesi, Maria Camilla; Calo', Girolamo; Janecka, Anna; Borics, Attila
Synthesis, biological properties and molecular modelling investigation of the first potent, selective and water soluble human A3 adenosine receptor antagonist.
file con accesso da definire2002 Maconi, A.; Pastorin, G.; Da Ros, T.; Spalluto, Giampiero; Gao, Z. G.; Jacobson, K. A.; Baraldi, Pier Giovanni; Cacciari, Barbara; Varani, Katia; Moro, S.; Borea, Pier Andrea
Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist
file con accesso da definire2002 Maconi, A; Pastorin, G; DA ROS, T; Spalluto, G; Gao, Zg; Jacobson, Ka; Baraldi, Pier Giovanni; Cacciari, Barbara; Varani, Katia; Moro, S; Borea, Pier Andrea
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Synthesis of the tritium labeled SCH 58261, a new non-xanthine A(2A) adenosine receptor antagonist | 1996 | Baraldi, Pier Giovanni; Cacciari, Barbara; Dionisotti, S; Egan, J; Spalluto, G; Zocchi, C. | file con accesso da definire |
Synthesis of thiourea-tethered C-glycosyl amino acids via isothiocyanate-amine coupling | 2009 | Barghash, R. F.; Massi, Alessandro; Dondoni, Alessandro | file con accesso da definire |
SYNTHESIS OF TRISACCHARIDE DERIVATIVES WITH THE SEQUENCE OF THE DESIALYLATED CAD BLOOD-GROUP DETERMINANT | 1985 | Catelani, G; Marra, Alberto; Paquet, F; Sinay, P. | file con accesso da definire |
Synthesis of Unsymmetrical Squaramides as Allosteric GSK-3β Inhibitors Promoting β-Catenin-Mediated Transcription of TCF/LEF in Retinal Pigment Epithelial Cells | 2022 | Carullo, G.; Bottoni, L.; Pasquini, S.; Papa, A.; Contri, C.; Brogi, S.; Calderone, V.; Orlandini..., M.; Gemma, S.; Varani, K.; Butini, S.; Galvagni, F.; Vincenzi, F.; Campiani, G. | |
synthesis stability evaluation and permeability study of a zidovudine-bile acid prodrug | 2011 | Dalpiaz, Alessandro; Fogagnolo, Marco; Pavan, Barbara; Perrone, Daniela; I., Poppi | file con accesso da definire |
Synthesis, antibacterial activity and structure-activity relationships of N-(pyridin-2-yl) 3-substituted-4-diazopyrazole-5-carboxamides | 1994 | Baraldi, Pier Giovanni; Brigidi, P.; Garuti, L.; Recanatini, M.; Roberti, M. | file con accesso da definire |
Synthesis, antibacterial activity and structure-activity relationships of N-substituted 3-methyl-4-diazo-5-pyrazolecarboxamides. | 1989 | Baraldi, Pier Giovanni; Brigidi, P.; Casolari, Alberto; Manfredini, Stefano; Periotto, V.; Recana...tini, M.; Roberti, M.; Rossi, M. | file con accesso da definire |
Synthesis, antibacterial activity and structure-activity relationships of N-substituted 4-diazopyrazole-5-carboxamides. 2 | 1991 | Baraldi, Pier Giovanni; Cacciari, Barbara; Leoni, Alberto; Recanatini, Maurizio; Roberti, Marinel...la; Rossi, Maddalena; Manfredini, Stefano; Periotto, Vittorio; Simoni, Daniele | file con accesso da definire |
Synthesis, Antimitotic and Antivascular Activity of 1-(3’,4’,5’-Trimethoxybenzoyl)-3-Arylamino-5-Amino-1,2,4-Triazoles | 2014 | Romagnoli, Romeo; Baraldi, Pier Giovanni; Kimatrai Salvador, M.; Prencipe, Filippo; Bertolasi, Va...lerio; Cancellieri, M.; Brancale, A.; Hamel, E.; Castagliuolo, I.; Consolaro, F.; Porcù, E.; Basso, G.; Viola, G. | file con accesso da definire |
Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications | 2012 | Baldisserotto, Anna; Malisardi, Gemma; Scalambra, Emanuela; Andreotti, Elisa; C., Romagnoli; Vice...ntini, Chiara Beatrice; Manfredini, Stefano; Vertuani, Silvia | file con accesso da definire |
Synthesis, antiviral and antiproliferative activity of a new class of 5-(alkyl or arylthio)-6-vinyl uracils | 1996 | Baraldi, Pier Giovanni; Cacciari, Barbara; Romagnoli, Romeo; Spalluto, G; Garuti, L; Roberti, M; ...Pani, A; Perra, G; Scintu, F; Pinna, N; Musiu, C; Lacolla, P. | file con accesso da definire |
Synthesis, binding and thermodynamic studies of new highly selective A2A adenosine receptor antagonists | 1997 | Cacciari, Barbara; Baraldi, Pier Giovanni; Spalluto, Giampiero; Ongini, E.; Dionisotti, S.; Varan...i, Katia; Gessi, Stefania; Borea, Pier Andrea | file con accesso da definire |
Synthesis, Biological Activity and Molecular Docking of Chimeric Peptides Targeting Opioid and NOP Receptors | 2022 | Wtorek, Karol; Ghidini, Alessia; Gentilucci, Luca; Adamska-Bartłomiejczyk, Anna; Piekielna-Ciesie...lska, Justyna; Ruzza, Chiara; Sturaro, Chiara; Calò, Girolamo; Pieretti, Stefano; Kluczyk, Alicja; Mcdonald, John; Lambert, David G; Janecka, Anna | |
Synthesis, biological activity and molecular modeling studies of 1,2,3,4-tetrahydroisoquinoline derivatives as conformationally constrained analogues of KN62, a potent antagonist of the P2X(7)-receptor containing a tyrosine moiety | 2002 | Baraldi, Pier Giovanni; Makaeva, R; Pavani, Maria Giovanna; Nunez, Md; Spalluto, G; Moro, S; Falz...oni, S; DI VIRGILIO, Francesco; Romagnoli, Romeo | file con accesso da definire |
Synthesis, biological activity, and molecular modeling investigation of new pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as human A(3) adenosine receptor antagonists | 2002 | Baraldi, Pier Giovanni; Cacciari, Barbara; Moro, S; Spalluto, G; Pastorin, G; DA ROS, T; Klotz, K...n; Varani, Katia; Gessi, Stefania; Borea, Pier Andrea | file con accesso da definire |
Synthesis, biological and modeling studies of new water soluble hA3 adenosine receptor antagonists. | 2005 | Pastorin, G.; Da Ros, T.; Bolcato, C.; Montopoli, C.; Moro, S.; Cacciari, Barbara; Baraldi, Pier ...Giovanni; Varani, Katia; Borea, Pier Andrea; Spalluto, G. | file con accesso da definire |
Synthesis, biological evaluation and docking studies of a novel class of sulfur-bridged diazabicyclo[3.3.1]nonanes | 2020 | Murineddu, Gabriele; Asproni, Battistina; Corona, Paola; Gessi, Stefania; Merighi, Stefania; Batt...istello, Enrica; Sturaro, Chiara; Calo', Girolamo; Galeotti, Nicoletta; Temml, Veronika; Herdlinger, Sonja; Schuster, Daniela; Pinna, Gerard A. | |
Synthesis, biological evaluation and structural analysis of novel peripherally active morphiceptin analogs | 2016 | Adamska, Anna; Kluczyk, Alicja; Cerlesi, Maria Camilla; Calo', Girolamo; Janecka, Anna; Borics, A...ttila | file con accesso da definire |
Synthesis, biological properties and molecular modelling investigation of the first potent, selective and water soluble human A3 adenosine receptor antagonist. | 2002 | Maconi, A.; Pastorin, G.; Da Ros, T.; Spalluto, Giampiero; Gao, Z. G.; Jacobson, K. A.; Baraldi, ...Pier Giovanni; Cacciari, Barbara; Varani, Katia; Moro, S.; Borea, Pier Andrea | file con accesso da definire |
Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist | 2002 | Maconi, A; Pastorin, G; DA ROS, T; Spalluto, G; Gao, Zg; Jacobson, Ka; Baraldi, Pier Giovanni; Ca...cciari, Barbara; Varani, Katia; Moro, S; Borea, Pier Andrea | file con accesso da definire |
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