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Binding of the prototypical adenosine A2A receptor agonist CGS 21680 to the cerebral cortex of adenosine A1 and A2Areceptor knockout miceLOPES, Luisa V; HALLDNER, Linda; REBOLA, Nelson et al.British journal of pharmacology. 2004, Vol 141, Num 6, pp 1006-1014, issn 0007-1188, 9 p.Article

Binding of the radioligand [3H]-SCH 58261, a new non-xanthine A2A adenosine receptor antagonist, to rat striatal membranesZOCCHI, C; ONGINI, E; FERRARA, S et al.British journal of pharmacology. 1996, Vol 117, Num 7, pp 1381-1386, issn 0007-1188Article

Adenosine A2A receptor antagonists are potential antidepressants : evidence based on pharmacology and A2A receptor knockout miceEL YACOUBI, Malika; LEDENT, Catherine; PARMENTIER, Marc et al.British journal of pharmacology. 2001, Vol 134, Num 1, pp 68-77, issn 0007-1188Article

Lack of tolerance to motor stimulant effects of a selective adenosine A2A receptor antagonistHALLDNER, Linda; LOZZA, Gianluca; LINDSTRÖM, Karin et al.European journal of pharmacology. 2000, Vol 406, Num 3, pp 345-354, issn 0014-2999Article

Caffeine reduces hypnotic effects of alcohol through adenosine A2A receptor blockadeEL YACOUBI, M; LEDENT, C; PARMENTIER, M et al.Neuropharmacology. 2003, Vol 45, Num 7, pp 977-985, issn 0028-3908, 9 p.Article

Characterization of human A2A adenosine receptors with the antagonist radioligand [3H]-SCH 58261DIONISOTTI, S; ONGINI, E; ZOCCHI, C et al.British journal of pharmacology. 1997, Vol 121, Num 3, pp 353-360, issn 0007-1188Article

Adenosine and memory storage : effect of A1 and A2 receptor antagonistsKOPF, S. R; MELANI, A; PEDATA, F et al.Psychopharmacologia. 1999, Vol 146, Num 2, pp 214-219, issn 0033-3158Article

Neuropharmacology of the adenosine A2A receptorsONGINI, E; DIONISOTTI, S; MORELLI, M et al.Drug development research. 1996, Vol 39, Num 3-4, pp 450-460, issn 0272-4391Conference Paper

Adenosine's role in hypercapnia-evoked cerebral vasodilation in the ratPHILLIS, J. W; LUNGU, C. L; BARBU, D. E et al.Neuroscience letters. 2004, Vol 365, Num 1, pp 6-9, issn 0304-3940, 4 p.Article

SCH 58261 differentially influences quinolinic acid-induced effects in striatal and in hippocampal slicesTEBANO, Maria Teresa; DOMENICI, Maria Rosaria; POPOLI, Patrizia et al.European journal of pharmacology. 2002, Vol 450, Num 3, pp 253-257, issn 0014-2999Article

Selective adenosine A2A receptor antagonistsONGINI, Ennio; MONOPOLI, Angela; CACCIARI, Barbara et al.Il Farmaco (Pavia). 2001, Vol 56, Num 1-2, pp 87-90, issn 0014-827XConference Paper

Blockade of adenosine A2A receptors by SCH 58261 results in neuroprotective effects in cerebral ischaemia in ratsMONOPOLI, A; LOZZA, G; FORLANI, A et al.Neuroreport (Oxford). 1998, Vol 9, Num 17, pp 3955-3959, issn 0959-4965Article

4-Amino-6-benzylamino-1,2-dihydro-2-phenyl-1,2,4-triazolo[4,5-a]-quinoxalin-1-on e : A new A2A adenosine receptor antagonist with high selectivity versus A1 receptorsCOLOTTA, V; CATARZI, D; VARANO, F et al.Archiv der Pharmazie (Weinheim). 1999, Vol 332, Num 2, pp 39-41, issn 0365-6233Article

Design, synthesis, and biological evaluation of C9- and C2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as new A2A and A3 adenosine receptors antagonistsBARALDI, Pier Giovanni; FRUTTAROLO, Francesca; BOREA, Pier Andrea et al.Journal of medicinal chemistry (Print). 2003, Vol 46, Num 7, pp 1229-1241, issn 0022-2623, 13 p.Article

SCH 58261 (an adenosine A2A receptor antagonist) reduces, only at low doses, K+-evoked glutamate release in the striatumPINTOR, Annita; QUARTA, Davide; PEZZOLA, Antonella et al.European journal of pharmacology. 2001, Vol 421, Num 3, pp 177-180, issn 0014-2999Article

Synthesis of the tritium labeled SCH 58261, a new non-xanthine A2A adenosine receptor antagonistBARALDI, P. G; CACCIARI, B; DIONISOTTI, S et al.Journal of labelled compounds & radiopharmaceuticals. 1996, Vol 38, Num 8, pp 725-732, issn 0362-4803Article

Modulation by adenosine A2A receptors of dopamine-mediated motor behavior as a basis for antiparkinson's disease drugsMORELLI, Micaela; PINNA, Annalisa.Drug development research. 2001, Vol 52, Num 1-2, pp 387-393, issn 0272-4391Conference Paper

SCH 58261 : A selective A2A adenosine receptor antagonistONGINI, E.Drug development research. 1997, Vol 42, Num 2, pp 63-70, issn 0272-4391Article

Dual actions of A2A adenosine receptor antagonists on motor dysfunction and neurodegenerative processesONGINI, Ennio; MONOPOLI, Angela; IMPAGNATIELLO, Francesco et al.Drug development research. 2001, Vol 52, Num 1-2, pp 379-386, issn 0272-4391Conference Paper

Increased adenosine A2A receptors in the brain of Parkinson's disease patients with dyskinesiasCALON, Frédéric; DRIDI, Mehdi; HORNYKIEWICZ, Oleh et al.Brain. 2004, Vol 127, pp 1075-1084, issn 0006-8950, 10 p., 5Article

Effects of SCH 58261, an adenosine A2A receptor antagonist, on quinpirole-induced turning in 6-hydroxydopamine-lesioned rats : Lack of tolerance after chronic caffeine intakePOPOLI, P; REGGIO, R; PEZZOLA, A et al.Neuropsychopharmacology (New York, NY). 2000, Vol 22, Num 5, pp 522-529, issn 0893-133XArticle

Selective blockade of A2A receptor protects against neurotoxicity induced by kainic acid in young ratsBORTOLATTO, Cristiani F; JESSE, Cristiano R; WILHELM, Ethel A et al.Fundamental & clinical pharmacology. 2012, Vol 26, Num 4, pp 495-502, issn 0767-3981, 8 p.Article

Adenosine A2A and dopamine receptor interactions in basal ganglia of dopamine denervated ratsCARTA, Anna R; PINNA, Annalisa; TRONCI, Elisabetta et al.Neurology. 2003, Vol 61, Num 11, pp S39-S43, issn 0028-3878, SUP6Article

Biaryl and heteroaryl derivatives of SCH 58261 as potent and selective adenosine A2A receptor antagonistsSHAH, Unmesh; BOYLE, Craig D; SHIYONG WANG et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 14, pp 4199-4203, issn 0960-894X, 5 p.Article

Design, synthesis, and evaluation of fused heterocyclic analogs of SCH 58261 as adenosine A2A receptor antagonistsSHAH, Unmesh; LANKIN, Claire M; HONGTAO ZHANG et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 14, pp 4204-4209, issn 0960-894X, 6 p.Article

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