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Disambiguation of "Spalluto, G."

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Synthesis, biological activity, and molecular modeling investigation of new pyrazolo4,3-e-1,2,4-triazolo1,5-cpyrimidine derivatives as human A(3) adenosine receptor antagonists

, , , , , , , , , and . J Med Chem, 45 (4): 770-80 (February 2002)Baraldi, Pier Giovanni Cacciari, Barbara Moro, Stefano Spalluto, Giampiero Pastorin, Giorgia Da Ros, Tatiana Klotz, Karl-Norbert Varani, Katia Gessi, Stefania Borea, Pier Andrea Research Support, Non-U.S. Gov't United States Journal of medicinal chemistry J Med Chem. 2002 Feb 14;45(4):770-80..

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Giuseppe G G Manzardo

G Baumann

G Lüers

G Schweitzer

G Dohmen

 

Other publications of authors with the same name

Exploring potency and selectivity receptor antagonist profiles using a multilabel classification approach: the human adenosine receptors as a key study, , , , , , , , and . J Chem Inf Model, 49 (12): 2820-36 (December 2009)Michielan, Lisa Stephanie, Federico Terfloth, Lothar Hristozov, Dimitar Cacciari, Barbara Klotz, Karl-Norbert Spalluto, Giampiero Gasteiger, Johann Moro, Stefano Research Support, Non-U.S. Gov't United States Journal of chemical information and modeling J Chem Inf Model. 2009 Dec;49(12):2820-36..New 2,6,9-trisubstituted adenines as adenosine receptor antagonists: a preliminary SAR profile, , , , , , , and . Purinergic Signal, 3 (4): 339-46 (September 2007)Lambertucci, Catia Cristalli, Gloria Dal Ben, Diego Kachare, Dhuldeo D Bolcato, Chiara Klotz, Karl-Norbert Spalluto, Giampiero Volpini, Rosaria Netherlands Purinergic signalling Purinergic Signal. 2007 Sep;3(4):339-46. Epub 2007 Sep 19..Linear and nonlinear 3D-QSAR approaches in tandem with ligand-based homology modeling as a computational strategy to depict the pyrazolo-triazolo-pyrimidine antagonists binding site of the human adenosine A2A receptor, , , , , , , , , and . J Chem Inf Model, 48 (2): 350-63 (February 2008)Michielan, Lisa Bacilieri, Magdalena Schiesaro, Andrea Bolcato, Chiara Pastorin, Giorgia Spalluto, Giampiero Cacciari, Barbara Klotz, Karl Norbet Kaseda, Chosei Moro, Stefano Research Support, Non-U.S. Gov't United States Journal of chemical information and modeling J Chem Inf Model. 2008 Feb;48(2):350-63. Epub 2008 Jan 24..(3)HMRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors, , , , , , , , , and . Mol Pharmacol, 57 (5): 968-75 (May 2000)Varani, K Merighi, S Gessi, S Klotz, K N Leung, E Baraldi, P G Cacciari, B Romagnoli, R Spalluto, G Borea, P A United states Molecular pharmacology Mol Pharmacol. 2000 May;57(5):968-75..Synthesis, biological activity, and molecular modeling investigation of new pyrazolo4,3-e-1,2,4-triazolo1,5-cpyrimidine derivatives as human A(3) adenosine receptor antagonists, , , , , , , , , and . J Med Chem, 45 (4): 770-80 (February 2002)Baraldi, Pier Giovanni Cacciari, Barbara Moro, Stefano Spalluto, Giampiero Pastorin, Giorgia Da Ros, Tatiana Klotz, Karl-Norbert Varani, Katia Gessi, Stefania Borea, Pier Andrea Research Support, Non-U.S. Gov't United States Journal of medicinal chemistry J Med Chem. 2002 Feb 14;45(4):770-80..Synthesis, biological studies and molecular modeling investigation of 1,3-dimethyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro 1,2,4-triazolo 3,4-f-purines as potential adenosine receptor antagonists, , , , , , , and . Farmaco, 60 (4): 299-306 (April 2005)Pastorin, Giorgia Bolcato, Chiara Cacciari, Barbara Kachler, Sonja Klotz, Karl-Norbert Montopoli, Christian Moro, Stefano Spalluto, Giampiero Research Support, Non-U.S. Gov't Italy Farmaco (Societa chimica italiana : 1989) Farmaco. 2005 Apr;60(4):299-306..Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: A complete structure-activity profile, , , , , , and . Purinergic Signal, 3 (3): 183-93 (June 2007)Cacciari, Barbara Bolcato, Chiara Spalluto, Giampiero Klotz, Karl-Norbet Bacilieri, Magdalena Deflorian, Francesca Moro, Stefano Netherlands Purinergic signalling Purinergic Signal. 2007 Jun;3(3):183-93. Epub 2006 Nov 14..Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypes, , , , , , , and . Purinergic Signal, 4 (1): 39-46 (March 2008)Bolcato, Chiara Cusan, Claudia Pastorin, Giorgia Spalluto, Giampiero Cacciari, Barbara Klotz, Karl Norbert Morizzo, Erika Moro, Stefano Netherlands Purinergic signalling Purinergic Signal. 2008 Mar;4(1):39-46. Epub 2007 Jul 25..Pyrazolo4,3-e1,2,4-triazolo1,5-cpyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists: influence of the chain at the N(8) pyrazole nitrogen, , , , , , , , , and 1 other author(s). J Med Chem, 43 (25): 4768-80 (December 2000)Baraldi, P G Cacciari, B Romagnoli, R Spalluto, G Moro, S Klotz, K N Leung, E Varani, K Gessi, S Merighi, S Borea, P A Research Support, Non-U.S. Gov't United states Journal of medicinal chemistry J Med Chem. 2000 Dec 14;43(25):4768-80..Pyrazolo4,3-e-1,2,4-triazolo1,5-cpyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists, , , , , , , , , and . J Med Chem, 42 (22): 4473-8 (November 1999)Baraldi, P G Cacciari, B Romagnoli, R Spalluto, G Klotz, K N Leung, E Varani, K Gessi, S Merighi, S Borea, P A In Vitro Research Support, Non-U.S. Gov't United states Journal of medicinal chemistry J Med Chem. 1999 Nov 4;42(22):4473-8..