-
1
-
-
0028183014
-
-
Fredholm, B. B.; Abbracchio, M. P.; Burnstock, G.; Daly, J. W.; Harden, T. K.; Jacobson, K. A.; Leff, P.; Williams, M. Nomenclature and classification of purinoceptors. Pharmacol. Rev., 1994, 46, 143-156.
-
(1994)
Nomenclature and classification of purinoceptors. Pharmacol. Rev
, vol.46
, pp. 143-156
-
-
Fredholm, B.B.1
Abbracchio, M.P.2
Burnstock, G.3
Daly, J.W.4
Harden, T.K.5
Jacobson, K.A.6
Leff, P.7
Williams, M.8
-
2
-
-
0034750364
-
Recent advances in adenosine receptor antagonist research
-
Hess, S. Recent advances in adenosine receptor antagonist research. Expert Opin. Ther. Patents, 2001, 11, 1533-1561.
-
(2001)
Expert Opin. Ther. Patents
, vol.11
, pp. 1533-1561
-
-
Hess, S.1
-
3
-
-
33947310062
-
-
Ishiwata, K.; Kimura, Y.; De Vries, Erik F. J.; Elsinga, P. H. PET Tracers for Mapping Adenosine Receptors as Probes for Diagnosis of CNS Disorders. Cent. Nerv. Syst. Agents Med. Chem., 2007, 7, 57-77.
-
(2007)
PET Tracers for Mapping Adenosine Receptors As Probes for Diagnosis of CNS Disorders. Cent. Nerv. Syst. Agents Med. Chem
, vol.7
, pp. 57-77
-
-
Ishiwata, K.1
Kimura, Y.2
De Vries Erik, F.J.3
Elsinga, P.H.4
-
5
-
-
17844371308
-
Adenosine in tissue protection and tissue regeneration
-
Linden, J. Adenosine in Tissue Protection and Tissue Regeneration. Mol. Pharmacol., 2005, 67, 1385-1387.
-
(2005)
Mol. Pharmacol
, vol.67
, pp. 1385-1387
-
-
Linden, J.1
-
6
-
-
0034923094
-
The role and regulation of adenosine in the central nervous system
-
Dunwiddie, T.; Masino, S. The role and regulation of adenosine in the central nervous system. Annu. Rev. Neurosci., 2001, 24, 31-55.
-
(2001)
Annu. Rev. Neurosci
, vol.24
, pp. 31-55
-
-
Dunwiddie, T.1
Masino, S.2
-
7
-
-
0035069332
-
Adenosine in the treatment of stroke: Yes, maybe, or absolutely not? Expert Opin
-
von Lubitz, D. K. Adenosine in the treatment of stroke: yes, maybe, or absolutely not? Expert Opin. Investig. Drugs, 2001, 10, 619-632.
-
(2001)
Investig. Drugs
, vol.10
, pp. 619-632
-
-
Von Lubitz, D.K.1
-
8
-
-
0036973951
-
Adenosine receptors in the nervous system: Pathophysiological implications
-
Ribeiro, J. A.; Sebastião, A. M.; de Mendonça, A. Adenosine receptors in the nervous system: pathophysiological implications. Prog. Neurobiol., 2002, 68, 377-392.
-
(2002)
Prog. Neurobiol
, vol.68
, pp. 377-392
-
-
Ribeiro, J.A.1
Sebastião, A.M.2
De Mendonça, A.3
-
9
-
-
33644770260
-
Adenosine receptors as therapeutic targets
-
Jacobson, K. A.; Gao, Z. Adenosine receptors as therapeutic targets. Nat. Rev. Drug Discov., 2006, 5, 247-264.
-
(2006)
Nat. Rev. Drug Discov
, vol.5
, pp. 247-264
-
-
Jacobson, K.A.1
Gao, Z.2
-
10
-
-
0345600929
-
Adenosine A2A receptors and depression
-
El Yacoubi, M.; Costentin, J.; Vaugeois, J. M. Adenosine A2A receptors and depression. Neurology, 2003, 61, S82-S87.
-
(2003)
Neurology
, vol.61
-
-
El Yacoubi, M.1
Costentin, J.2
Vaugeois, J.M.3
-
11
-
-
0037038328
-
Synthesis and Evaluation of No-Carrier-Added 8-Cyclopentyl-3-(3-[18F] fluoropropyl)-1- propylxanthine ([18F]CPFPX): A Potent and Selective A1- Adenosine Receptor Antagonist for in Vivo Imaging
-
Holschbach, M. H.; Olsson, R. A.; Bier, D.; Wutz, W.; Sihver, W.; Schüller, M.; Palm, B.; Coenen, H. H. Synthesis and Evaluation of No-Carrier-Added 8-Cyclopentyl-3-(3-[18F]fluoropropyl)-1- propylxanthine ([18F]CPFPX): A Potent and Selective A1- Adenosine Receptor Antagonist for in Vivo Imaging. J. Med. Chem., 2002, 45, 5150-5156.
-
(2002)
J. Med. Chem
, vol.45
, pp. 5150-5156
-
-
Holschbach, M.H.1
Olsson, R.A.2
Bier, D.3
Wutz, W.4
Sihver, W.5
Schüller, M.6
Palm, B.7
Coenen, H.H.8
-
12
-
-
80054872347
-
Adenosine A(1) receptors in the central nervous system: Their functions in health and disease, and possible elucidation by PET imaging
-
Paul, S.; Elsinga, P. H.; Ishiwata, K.; Dierckx, R. A.; van Waarde, A. Adenosine A(1) receptors in the central nervous system: their functions in health and disease, and possible elucidation by PET imaging. Curr. Med. Chem., 2011, 18, 4820-4835.
-
(2011)
Curr. Med. Chem
, vol.18
, pp. 4820-4835
-
-
Paul, S.1
Elsinga, P.H.2
Ishiwata, K.3
Dierckx, R.A.4
Van Waarde, A.5
-
13
-
-
69249202366
-
Triggering neurotrophic factor actions through adenosine A2A receptor activation: Implications for neuroprotection
-
Sebastião, A. M.; Ribeiro, J. A. Triggering neurotrophic factor actions through adenosine A2A receptor activation: implications for neuroprotection. Br. J. Pharmacol., 2009, 158, 15-22.
-
(2009)
Br. J. Pharmacol
, vol.158
, pp. 15-22
-
-
Sebastião, A.M.1
Ribeiro, J.A.2
-
14
-
-
0031754497
-
Receptors for purines and pyrimidines
-
Ralevic, V.; Burnstock, G. Receptors for Purines and Pyrimidines. Pharmacol. Rev., 1998, 50, 413-492.
-
(1998)
Pharmacol. Rev
, vol.50
, pp. 413-492
-
-
Ralevic, V.1
Burnstock, G.2
-
15
-
-
0026590186
-
Characterization of human striatal A2-adenosine receptors using radioligand binding and photoaffinity labeling
-
Ji, X. D.; Stiles, G. L.; van Galen, P. J.; Jacobson, K. A. Characterization of human striatal A2-adenosine receptors using radioligand binding and photoaffinity labeling. J. Recept. Res., 1992, 12, 149-169.
-
(1992)
J. Recept. Res
, vol.12
, pp. 149-169
-
-
Ji, X.D.1
Stiles, G.L.2
Van Galen, P.J.3
Jacobson, K.A.4
-
16
-
-
0020355715
-
Autoradiographic localization of adenosine receptors in rat brain using [3H]cyclohexyladenosine
-
Goodman, R. R.; Synder, S. H. Autoradiographic localization of adenosine receptors in rat brain using [3H]cyclohexyladenosine. J. Neurosci., 1982, 2, 1230-1241.
-
(1982)
J. Neurosci
, vol.2
, pp. 1230-1241
-
-
Goodman, R.R.1
Synder, S.H.2
-
17
-
-
0029658870
-
The selective adenosine A2A receptor antagonist SCH 58261 discriminates between two different binding sites for [3H]-CGS 21680 in the rat brain
-
Lindstrom, K.; Ongini, E.; Fredholm, B. B. The selective adenosine A2A receptor antagonist SCH 58261 discriminates between two different binding sites for [3H]-CGS 21680 in the rat brain. Naunyn Schmiedebergs Arch. Pharmacol., 1996, 354, 539-541.
-
(1996)
Naunyn Schmiedebergs Arch. Pharmacol
, vol.354
, pp. 539-541
-
-
Lindstrom, K.1
Ongini, E.2
Fredholm, B.B.3
-
18
-
-
0030250999
-
Pharmacology of adenosine A2A receptors
-
Ongini, E.; Fredholm, B. B. Pharmacology of adenosine A2A receptors. Trends Pharmacol. Sci., 1996, 17, 364-372.
-
(1996)
Trends Pharmacol. Sci
, vol.17
, pp. 364-372
-
-
Ongini, E.1
Fredholm, B.B.2
-
19
-
-
79952033865
-
International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and classification of adenosine receptors - An update
-
Fredholm, B. B.; IJzerman, A. P.; Jacobson, K. A.; Linden, J.; Muller, C. E. International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and classification of adenosine receptors - an update. Pharmacol. Rev., 2011, 63, 1-34.
-
(2011)
Pharmacol. Rev
, vol.63
, pp. 1-34
-
-
Fredholm, B.B.1
Ijzerman, A.P.2
Jacobson, K.A.3
Linden, J.4
Muller, C.E.5
-
20
-
-
0033408368
-
Central adenosine A2A receptors: An overview
-
Moreau, J.; Huber, G. Central adenosine A2A receptors: an overview. Brain Res. Rev., 1999, 31, 65-82.
-
(1999)
Brain Res. Rev
, vol.31
, pp. 65-82
-
-
Moreau, J.1
Huber, G.2
-
21
-
-
33750077251
-
Review of the therapeutic management of Parkinson's disease. Report of a joint task force of the European Federation of Neurological Societies (EFNS) and the Movement Disorder Society-European Section (MDS-ES). Part II: Late (complicated) Parkinson's disease
-
Horstink, M.; Tolosa, E.; Bonuccelli, U.; Deuschl, G.; Friedman, A.; Kanovsky, P.; Larsen, J. P.; Lees, A.; Oertel, W.; Poewe, W.; Rascol, O.; Sampaio, C. Review of the therapeutic management of Parkinson's disease. Report of a joint task force of the European Federation of Neurological Societies (EFNS) and the Movement Disorder Society-European Section (MDS-ES). Part II: late (complicated) Parkinson's disease. Eur. J. Neurol., 2006, 13, 1186-1202.
-
(2006)
Eur. J. Neurol
, vol.13
, pp. 1186-1202
-
-
Horstink, M.1
Tolosa, E.2
Bonuccelli, U.3
Deuschl, G.4
Friedman, A.5
Kanovsky, P.6
Larsen, J.P.7
Lees, A.8
Oertel, W.9
Poewe, W.10
Rascol, O.11
Sampaio, C.12
-
22
-
-
33750067356
-
Review of the therapeutic management of Parkinson's disease. Report of a joint task force of the European Federation of Neurological Societies and the Movement Disorder Society? European Section. Part I: Early (uncomplicated) Parkinson's disease
-
Horstink, M.; Tolosa, E.; Bonuccelli, U.; Deuschl, G.; Friedman, A.; Kanovsky, P.; Larsen, J. P.; Lees, A.; Oertel, W.; Poewe, W.; Rascol, O.; Sampaio, C. Review of the therapeutic management of Parkinson's disease. Report of a joint task force of the European Federation of Neurological Societies and the Movement Disorder Society? European Section. Part I: early (uncomplicated) Parkinson's disease. Eur. J. Neurol., 2006, 13, 1170-1185.
-
(2006)
Eur. J. Neurol
, vol.13
, pp. 1170-1185
-
-
Horstink, M.1
Tolosa, E.2
Bonuccelli, U.3
Deuschl, G.4
Friedman, A.5
Kanovsky, P.6
Larsen, J.P.7
Lees, A.8
Oertel, W.9
Poewe, W.10
Rascol, O.11
Sampaio, C.12
-
23
-
-
34548030225
-
Levodopa-induced dyskinesias
-
quiz 1523
-
Fabbrini, G.; Brotchie, J. M.; Grandas, F.; Nomoto, M.; Goetz, C. G. Levodopa-induced dyskinesias. Mov. Disord., 2007, 22, 1379- 89; quiz 1523.
-
(2007)
Mov. Disord
, vol.22
, pp. 1379-1389
-
-
Fabbrini, G.1
Brotchie, J.M.2
Grandas, F.3
Nomoto, M.4
Goetz, C.G.5
-
24
-
-
20444489689
-
Motor fluctuations and dyskinesias in Parkinson's disease: Clinical manifestations
-
Jankovic, J. Motor fluctuations and dyskinesias in Parkinson's disease: clinical manifestations. Mov. Disord., 2005, 20 Suppl 11, S11-S16.
-
(2005)
Mov. Disord
, vol.20
, Issue.SUPPL. 11
-
-
Jankovic, J.1
-
25
-
-
34547191858
-
Medical management of levodopaassociated motor complications in patients with Parkinson's disease
-
Jankovic, J.; Stacy, M. Medical management of levodopaassociated motor complications in patients with Parkinson's disease. CNS Drugs, 2007, 21, 677-692.
-
(2007)
CNS Drugs
, vol.21
, pp. 677-692
-
-
Jankovic, J.1
Stacy, M.2
-
26
-
-
70349327971
-
Adenosine A2A receptors and Parkinson's disease
-
Morelli, M.; Carta, A. R.; Jenner, P. Adenosine A2A receptors and Parkinson's disease. Handb. Exp. Pharmacol., 2009, 193, 589-615.
-
(2009)
Handb. Exp. Pharmacol
, vol.193
, pp. 589-615
-
-
Morelli, M.1
Carta, A.R.2
Jenner, P.3
-
27
-
-
0037015027
-
Synergistic interaction between adenosine A2A and glutamate mGlu5 receptors: Implications for striatal neuronal function
-
Ferre, S.; Karcz-Kubicha, M.; Hope, B. T.; Popoli, P.; Burgueno, J.; Gutierrez, M. A.; Casado, V.; Fuxe, K.; Goldberg, S. R.; Lluis, C.; Franco, R.; Ciruela, F. Synergistic interaction between adenosine A2A and glutamate mGlu5 receptors: implications for striatal neuronal function. Proc. Natl. Acad. Sci. U. S. A., 2002, 99, 11940-11945.
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 11940-11945
-
-
Ferre, S.1
Karcz-Kubicha, M.2
Hope, B.T.3
Popoli, P.4
Burgueno, J.5
Gutierrez, M.A.6
Casado, V.7
Fuxe, K.8
Goldberg, S.R.9
Lluis, C.10
Franco, R.11
Ciruela, F.12
-
28
-
-
3242765264
-
Simultaneous blockade of adenosine A2A and metabotropic glutamate mGlu5 receptors increase their efficacy in reversing Parkinsonian deficits in rats
-
Coccurello, R.; Breysse, N.; Amalric, M. Simultaneous blockade of adenosine A2A and metabotropic glutamate mGlu5 receptors increase their efficacy in reversing Parkinsonian deficits in rats. Neuropsychopharmacology, 2004, 29, 1451-1461.
-
(2004)
Neuropsychopharmacology
, vol.29
, pp. 1451-1461
-
-
Coccurello, R.1
Breysse, N.2
Amalric, M.3
-
29
-
-
36148983766
-
Adenosine A2A receptors and basal ganglia physiology
-
Schiffmann, S. N.; Fisone, G.; Moresco, R.; Cunha, R. A.; Ferre, S. Adenosine A2A receptors and basal ganglia physiology. Prog. Neurobiol., 2007, 83, 277-292.
-
(2007)
Prog. Neurobiol
, vol.83
, pp. 277-292
-
-
Schiffmann, S.N.1
Fisone, G.2
Moresco, R.3
Cunha, R.A.4
Ferre, S.5
-
30
-
-
58149096475
-
Looking for the role of cannabinoid receptor heteromers in striatal function
-
Ferré, S.; Goldberg, S. R.; Lluis, C.; Franco, R. Looking for the role of cannabinoid receptor heteromers in striatal function. Neuropharmacology, 2009, 56, Supplement 1, 226-234.
-
(2009)
Neuropharmacology
, vol.56
, Issue.SUPPL. 1
, pp. 226-234
-
-
Ferré, S.1
Goldberg, S.R.2
Lluis, C.3
Franco, R.4
-
31
-
-
40849137554
-
Antagonistic cannabinoid CB1/dopamine D2 receptor interactions in striatal CB1/D2 heteromers. A combined neurochemical and behavioral analysis
-
Marcellino, D.; Carriba, P.; Filip, M.; Borgkvist, A.; Frankowska, M.; Bellido, I.; Tanganelli, S.; Muller, C. E.; Fisone, G.; Lluis, C.; Agnati, L. F.; Franco, R.; Fuxe, K. Antagonistic cannabinoid CB1/dopamine D2 receptor interactions in striatal CB1/D2 heteromers. A combined neurochemical and behavioral analysis. Neuropharmacology, 2008, 54, 815-823.
-
(2008)
Neuropharmacology
, vol.54
, pp. 815-823
-
-
Marcellino, D.1
Carriba, P.2
Filip, M.3
Borgkvist, A.4
Frankowska, M.5
Bellido, I.6
Tanganelli, S.7
Muller, C.E.8
Fisone, G.9
Lluis, C.10
Agnati, L.F.11
Franco, R.12
Fuxe, K.13
-
32
-
-
0028946706
-
Adenosine receptor subtypes: Characterization and therapeutic regulation
-
Olah, M. E.; Stiles, G. L. Adenosine receptor subtypes: characterization and therapeutic regulation. Annu. Rev. Pharmacol. Toxicol., 1995, 35, 581-606.
-
(1995)
Annu. Rev. Pharmacol. Toxicol
, vol.35
, pp. 581-606
-
-
Olah, M.E.1
Stiles, G.L.2
-
33
-
-
0032543955
-
A2Aadenosine receptor reserve for coronary vasodilation
-
Shryock, J. C.; Snowdy, S.; Baraldi, P. G.; Cacciari, B.; Spalluto, G.; Monopoli, A.; Ongini, E.; Baker, S. P.; Belardinelli, L. A2Aadenosine receptor reserve for coronary vasodilation. Circulation, 1998, 98, 711-718.
-
(1998)
Circulation
, vol.98
, pp. 711-718
-
-
Shryock, J.C.1
Snowdy, S.2
Baraldi, P.G.3
Cacciari, B.4
Spalluto, G.5
Monopoli, A.6
Ongini, E.7
Baker, S.P.8
Belardinelli, L.9
-
34
-
-
0030612311
-
Adenosine A2 receptor function in rat ventricular myocytes
-
Dobson, J. G.,Jr; Fenton, R. A. Adenosine A2 receptor function in rat ventricular myocytes. Cardiovasc. Res., 1997, 34, 337-347.
-
(1997)
Cardiovasc. Res
, vol.34
, pp. 337-347
-
-
Dobson Jr., J.G.1
Fenton, R.A.2
-
35
-
-
27144538224
-
Greater adenosine A2A receptor densities in cardiac and skeletal muscle in endurance- trained men: A [11C] TMSX PET study
-
Mizuno, M.; Kimura, Y.; Tokizawa, K.; Ishii, K.; Oda, K.; Sasaki, T.; Nakamura, Y.; Muraoka, I.; Ishiwata, K. Greater adenosine A2A receptor densities in cardiac and skeletal muscle in endurance- trained men: a [11C]TMSX PET study. Nucl. Med. Biol., 2005, 32, 831-836.
-
(2005)
Nucl. Med. Biol
, vol.32
, pp. 831-836
-
-
Mizuno, M.1
Kimura, Y.2
Tokizawa, K.3
Ishii, K.4
Oda, K.5
Sasaki, T.6
Nakamura, Y.7
Muraoka, I.8
Ishiwata, K.9
-
36
-
-
70349331089
-
Adenosine receptor ligands and PET imaging of the CNS
-
Bauer, A.; Ishiwata, K. Adenosine Receptor Ligands and PET Imaging of the CNS. Handb. Exp. Pharmacol., 2009, 193, 617-642.
-
(2009)
Handb. Exp. Pharmacol
, vol.193
, pp. 617-642
-
-
Bauer, A.1
Ishiwata, K.2
-
37
-
-
0036025117
-
Applications of adenosine receptor ligands in medical imaging by positron emission tomography
-
Holschbach, M. H.; Olsson, R. A. Applications of adenosine receptor ligands in medical imaging by positron emission tomography. Curr. Pharm. Des., 2002, 8, 2345-2352.
-
(2002)
Curr. Pharm. des
, vol.8
, pp. 2345-2352
-
-
Holschbach, M.H.1
Olsson, R.A.2
-
38
-
-
0034090878
-
Morphological and functional imaging studies on the diagnosis and progression of Parkinson's disease
-
Brooks, D. J. Morphological and functional imaging studies on the diagnosis and progression of Parkinson's disease. J. Neurol., 2000, 247, II11-II18.
-
(2000)
J. Neurol
, vol.247
-
-
Brooks D., .J.1
-
39
-
-
0141533021
-
Potential of an adenosine A2A receptor antagonist [11C] TMSX for myocardial imaging by positron emission tomography: A first human study
-
Ishiwata, K.; Kawamura, K.; Kimura, Y.; Oda, K.; Ishii, K. Potential of an adenosine A2A receptor antagonist [11C]TMSX for myocardial imaging by positron emission tomography: a first human study. Ann. Nucl. Med., 2003, 17, 457-462.
-
(2003)
Ann. Nucl. Med
, vol.17
, pp. 457-462
-
-
Ishiwata, K.1
Kawamura, K.2
Kimura, Y.3
Oda, K.4
Ishii, K.5
-
40
-
-
4644330956
-
Potential of [11C] TMSX for the evaluation of adenosine A2A receptors in the skeletal muscle by positron emission tomography
-
Ishiwata, K.; Mizuno, M.; Kimura, Y.; Kawamura, K.; Oda, K.; Sasaki, T.; Nakamura, Y.; Muraoka, I.; Ishii, K. Potential of [11C]TMSX for the evaluation of adenosine A2A receptors in the skeletal muscle by positron emission tomography. Nucl. Med. Biol., 2004, 31, 949-956.
-
(2004)
Nucl. Med. Biol
, vol.31
, pp. 949-956
-
-
Ishiwata, K.1
Mizuno, M.2
Kimura, Y.3
Kawamura, K.4
Oda, K.5
Sasaki, T.6
Nakamura, Y.7
Muraoka, I.8
Ishii, K.9
-
41
-
-
55349100125
-
Myocardial blood flow and adenosine A2A receptor density in endurance athletes and untrained men
-
Heinonen, I.; Nesterov, S. V.; Liukko, K.; Kemppainen, J.; Någren, K.; Luotolahti, M.; Virsu, P.; Oikonen, V.; Nuutila, P.; Kujala, U. M.; Kainulainen, H.; Boushel, R.; Knuuti, J.; Kalliokoski, K. K. Myocardial blood flow and adenosine A2A receptor density in endurance athletes and untrained men. J. Physiol., 2008, 586, 5193-5202.
-
(2008)
J. Physiol
, vol.586
, pp. 5193-5202
-
-
Heinonen, I.1
Nesterov, S.V.2
Liukko, K.3
Kemppainen, J.4
Någren, K.5
Luotolahti, M.6
Virsu, P.7
Oikonen, V.8
Nuutila, P.9
Kujala, U.M.10
Kainulainen, H.11
Boushel, R.12
Knuuti, J.13
Kalliokoski, K.K.14
-
42
-
-
84863476384
-
Differential effects of age on human striatal adenosine A(1) and A(2A) receptors
-
Mishina, M.; Kimura, Y.; Naganawa, M.; Ishii, K.; Oda, K.; Sakata, M.; Toyohara, J.; Kobayashi, S.; Katayama, Y.; Ishiwata, K. Differential effects of age on human striatal adenosine A(1) and A(2A) receptors. Synapse, 2012, 66, 832-839.
-
(2012)
Synapse
, vol.66
, pp. 832-839
-
-
Mishina, M.1
Kimura, Y.2
Naganawa, M.3
Ishii, K.4
Oda, K.5
Sakata, M.6
Toyohara, J.7
Kobayashi, S.8
Katayama, Y.9
Ishiwata, K.10
-
43
-
-
34547214859
-
Evaluation of distribution of adenosine A2A receptors in normal human brain measured with [11C]TMSX PET
-
Mishina, M.; Ishiwata, K.; Kimura, Y.; Naganawa, M.; Oda, K.; Kobayashi, S.; Katayama, Y.; Ishii, K. Evaluation of distribution of adenosine A2A receptors in normal human brain measured with [11C]TMSX PET. Synapse, 2007, 61, 778-784.
-
(2007)
Synapse
, vol.61
, pp. 778-784
-
-
Mishina, M.1
Ishiwata, K.2
Kimura, Y.3
Naganawa, M.4
Oda, K.5
Kobayashi, S.6
Katayama, Y.7
Ishii, K.8
-
44
-
-
34247579206
-
Quantification of adenosine A2A receptors in the human brain using [11C] TMSX and positron emission tomography
-
Naganawa, M.; Kimura, Y.; Mishina, M.; Manabe, Y.; Chihara, K.; Oda, K.; Ishii, K.; Ishiwata, K. Quantification of adenosine A2A receptors in the human brain using [11C]TMSX and positron emission tomography. Eur. J. Nucl. Med. Mol. Imaging, 2007, 34, 679-687.
-
(2007)
Eur. J. Nucl. Med. Mol. Imaging
, vol.34
, pp. 679-687
-
-
Naganawa, M.1
Kimura, Y.2
Mishina, M.3
Manabe, Y.4
Chihara, K.5
Oda, K.6
Ishii, K.7
Ishiwata, K.8
-
45
-
-
79952234223
-
Adenosine A2A Receptors Measured with [11C]TMSX PET in the Striata of Parkinson's Disease Patients
-
Mishina, M.; Ishiwata, K.; Naganawa, M.; Kimura, Y.; Kitamura, S.; Suzuki, M.; Hashimoto, M.; Ishibashi, K.; Oda, K.; Sakata, M.; Hamamoto, M.; Kobayashi, S.; Katayama, Y.; Ishii, K. Adenosine A2A Receptors Measured with [11C]TMSX PET in the Striata of Parkinson's Disease Patients. PLoS One, 2011, 6, e17338.
-
(2011)
PLoS One
, vol.6
-
-
Mishina, M.1
Ishiwata, K.2
Naganawa, M.3
Kimura, Y.4
Kitamura, S.5
Suzuki, M.6
Hashimoto, M.7
Ishibashi, K.8
Oda, K.9
Sakata, M.10
Hamamoto, M.11
Kobayashi, S.12
Katayama, Y.13
Ishii, K.14
-
46
-
-
47749149925
-
Positron emission tomography analysis of [11C]KW-6002 binding to human and rat adenosine A2A receptors in the brain
-
Brooks, D. J.; Doder, M.; Osman, S.; Luthra, S. K.; Hirani, E.; Hume, S.; Kase, H.; Kilborn, J.; Martindill, S.; Mori, A. Positron emission tomography analysis of [11C]KW-6002 binding to human and rat adenosine A2A receptors in the brain. Synapse, 2008, 62, 671-681.
-
(2008)
Synapse
, vol.62
, pp. 671-681
-
-
Brooks, D.J.1
Doder, M.2
Osman, S.3
Luthra, S.K.4
Hirani, E.5
Hume, S.6
Kase, H.7
Kilborn, J.8
Martindill, S.9
Mori, A.10
-
47
-
-
33947505232
-
Synergistic effects of adenosine A2A antagonist and LDOPA on rotational behaviors in 6-hydroxydopamine-induced hemi-Parkinsonian mouse model
-
Matsuya, T.; Takuma, K.; Sato, K.; Asai, M.; Murakami, Y.; Miyoshi, S.; Noda, A.; Nagai, T.; Mizoguchi, H.; Nishimura, S.; Yamada, K. Synergistic effects of adenosine A2A antagonist and LDOPA on rotational behaviors in 6-hydroxydopamine-induced hemi-Parkinsonian mouse model. J. Pharmacol. Sci., 2007, 103, 329-332.
-
(2007)
J. Pharmacol. Sci
, vol.103
, pp. 329-332
-
-
Matsuya, T.1
Takuma, K.2
Sato, K.3
Asai, M.4
Murakami, Y.5
Miyoshi, S.6
Noda, A.7
Nagai, T.8
Mizoguchi, H.9
Nishimura, S.10
Yamada, K.11
-
48
-
-
80051691328
-
Striatal adenosine A(2A) receptor-mediated positron emission tomographic imaging in 6-hydroxydopamine-lesioned rats using [(18)F]-MRS5425
-
Bhattacharjee, A. K.; Lang, L.; Jacobson, O.; Shinkre, B.; Ma, Y.; Niu, G.; Trenkle, W. C.; Jacobson, K. A.; Chen, X.; Kiesewetter, D. O. Striatal adenosine A(2A) receptor-mediated positron emission tomographic imaging in 6-hydroxydopamine-lesioned rats using [(18)F]-MRS5425. Nucl. Med. Biol., 2011, 38, 897-906.
-
(2011)
Nucl. Med. Biol
, vol.38
, pp. 897-906
-
-
Bhattacharjee, A.K.1
Lang, L.2
Jacobson, O.3
Shinkre, B.4
Ma, Y.5
Niu, G.6
Trenkle, W.C.7
Jacobson, K.A.8
Chen, X.9
Kiesewetter, D.O.10
-
49
-
-
79958163183
-
Adenosine 2A receptor availability in dyskinetic and nondyskinetic patients with Parkinson disease
-
Ramlackhansingh, A. F.; Bose, S. K.; Ahmed, I.; Turkheimer, F. E.; Pavese, N.; Brooks, D. J. Adenosine 2A receptor availability in dyskinetic and nondyskinetic patients with Parkinson disease. Neurology, 2011, 76, 1811-1816.
-
(2011)
Neurology
, vol.76
, pp. 1811-1816
-
-
Ramlackhansingh, A.F.1
Bose, S.K.2
Ahmed, I.3
Turkheimer, F.E.4
Pavese, N.5
Brooks, D.J.6
-
50
-
-
77951087570
-
An open-label, positron emission tomography study to assess adenosine A2A brain receptor occupancy of vipadenant (BIIB014) at steady-state levels in healthy male volunteers
-
Brooks, D. J.; Papapetropoulos, S.; Vandenhende, F.; Tomic, D.; He, P.; Coppell, A.; O'Neill, G. An open-label, positron emission tomography study to assess adenosine A2A brain receptor occupancy of vipadenant (BIIB014) at steady-state levels in healthy male volunteers. Clin. Neuropharmacol., 2010, 33, 55-60.
-
(2010)
Clin. Neuropharmacol
, vol.33
, pp. 55-60
-
-
Brooks, D.J.1
Papapetropoulos, S.2
Vandenhende, F.3
Tomic, D.4
He, P.5
Coppell, A.6
O'Neill, G.7
-
51
-
-
46449134214
-
Purinergic signalling and disorders of the central nervous system
-
Burnstock, G. Purinergic signalling and disorders of the central nervous system. Nat. Rev. Drug Discov., 2008, 7, 575-590.
-
(2008)
Nat. Rev. Drug Discov
, vol.7
, pp. 575-590
-
-
Burnstock, G.1
-
52
-
-
38749132550
-
Adenosine receptor antagonists: Translating medicinal chemistry and pharmacology into clinical utility
-
Baraldi, P. G.; Tabrizi, M. A.; Gessi, S.; Borea, P. A. Adenosine receptor antagonists: translating medicinal chemistry and pharmacology into clinical utility. Chem. Rev., 2008, 108, 238-263.
-
(2008)
Chem. Rev
, vol.108
, pp. 238-263
-
-
Baraldi, P.G.1
Tabrizi, M.A.2
Gessi, S.3
Borea, P.A.4
-
53
-
-
14544288232
-
Therapeutic potential of adenosine A2A receptor antagonists in Parkinson's disease
-
Xu, K.; Bastia, E.; Schwarzschild, M. Therapeutic potential of adenosine A2A receptor antagonists in Parkinson's disease. Pharmacol. Ther., 2005, 105, 267-310.
-
(2005)
Pharmacol. Ther
, vol.105
, pp. 267-310
-
-
Xu, K.1
Bastia, E.2
Schwarzschild, M.3
-
54
-
-
22344455811
-
Adenosine A2A receptor antagonists for Parkinson's disease: Rationale, therapeutic potential and clinical experience
-
Hauser, R. A.; Schwarzschild, M. A. Adenosine A2A receptor antagonists for Parkinson's disease: rationale, therapeutic potential and clinical experience. Drugs Aging, 2005, 22, 471-482.
-
(2005)
Drugs Aging
, vol.22
, pp. 471-482
-
-
Hauser, R.A.1
Schwarzschild, M.A.2
-
55
-
-
0036080003
-
A(2A) adenosine receptor: A novel therapeutic target in renal disease
-
Okusa, M. D. A(2A) adenosine receptor: a novel therapeutic target in renal disease. Am. J. Physiol. Renal Physiol., 2002, 282, F10-F18.
-
(2002)
Am. J. Physiol. Renal Physiol
, vol.282
-
-
Okusa, M.D.1
-
56
-
-
26444445618
-
New therapies for the treatment of Parkinson's disease: Adenosine A2A receptor antagonists
-
Pinna, A.; Wardas, J.; Simola, N.; Morelli, M. New therapies for the treatment of Parkinson's disease: adenosine A2A receptor antagonists. Life Sci., 2005, 77, 3259-3267.
-
(2005)
Life Sci
, vol.77
, pp. 3259-3267
-
-
Pinna, A.1
Wardas, J.2
Simola, N.3
Morelli, M.4
-
57
-
-
73449139510
-
Novel investigational adenosine A2A receptor antagonists for Parkinson's disease
-
Pinna, A. Novel investigational adenosine A2A receptor antagonists for Parkinson's disease. Expert Opin. Investig. Drugs, 2009, 18, 1619-1631.
-
(2009)
Expert Opin. Investig. Drugs
, vol.18
, pp. 1619-1631
-
-
Pinna, A.1
-
58
-
-
34548295509
-
Therapeutic potential of adenosine receptor antagonists and agonists
-
Press, N. J.; Gessi, S.; Borea, P. A.; Polosa, R. Therapeutic potential of adenosine receptor antagonists and agonists. Expert Opin. Ther. Pat., 2007, 17, 979-991.
-
(2007)
Expert Opin. Ther. Pat
, vol.17
, pp. 979-991
-
-
Press, N.J.1
Gessi, S.2
Borea, P.A.3
Polosa, R.4
-
59
-
-
47749126216
-
Highlights on the development of A(2A) adenosine receptor agonists and antagonists
-
Cristalli, G.; Cacciari, B.; Dal Ben, D.; Lambertucci, C.; Moro, S.; Spalluto, G.; Volpini, R. Highlights on the development of A(2A) adenosine receptor agonists and antagonists. ChemMedChem, 2007, 2, 260-281.
-
(2007)
ChemMedChem
, vol.2
, pp. 260-281
-
-
Cristalli, G.1
Cacciari, B.2
Dal Ben, D.3
Lambertucci, C.4
Moro, S.5
Spalluto, G.6
Volpini, R.7
-
60
-
-
0030152887
-
Synthesis and preliminary evaluation of [11C] KF17837, a selective adenosine A2A antagonist
-
Ishiwata, K.; Noguchi, J.; Toyama, H.; Sakiyama, Y.; Koike, N.; Ishii, S.; Oda, K.; Endo, K.; Suzuki, F.; Senda, M. Synthesis and preliminary evaluation of [11C]KF17837, a selective adenosine A2A antagonist. Appl. Radiat. Isot., 1996, 47, 507-511.
-
(1996)
Appl. Radiat. Isot
, vol.47
, pp. 507-511
-
-
Ishiwata, K.1
Noguchi, J.2
Toyama, H.3
Sakiyama, Y.4
Koike, N.5
Ishii, S.6
Oda, K.7
Endo, K.8
Suzuki, F.9
Senda, M.10
-
61
-
-
0033621991
-
11Clabeled KF18446: A potential central nervous system adenosine A2a receptor ligand
-
Ishiwata, K.; Noguchi, J.; Wakabayashi, S.; Shimada, J.; Ogi, N.; Nariai, T.; Tanaka, A.; Endo, K.; Suzuki, F.; Senda, M. 11Clabeled KF18446: a potential central nervous system adenosine A2a receptor ligand. J. Nucl. Med., 2000, 41, 345-354.
-
(2000)
J. Nucl. Med
, vol.41
, pp. 345-354
-
-
Ishiwata, K.1
Noguchi, J.2
Wakabayashi, S.3
Shimada, J.4
Ogi, N.5
Nariai, T.6
Tanaka, A.7
Endo, K.8
Suzuki, F.9
Senda, M.10
-
62
-
-
0030911839
-
In vivo biodistribution of [N-11C-methyl]KF 17837 using 3-D-PET: Evaluation as a ligand for the study of adenosine A2A receptors
-
Stone-Elander, S.; Thorell, J.; Eriksson, L.; Fredholm, B. B.; Ingvar, M. In vivo biodistribution of [N-11C-methyl]KF 17837 using 3-D-PET: Evaluation as a ligand for the study of adenosine A2A receptors. Nucl. Med. Biol., 1997, 24, 187-191.
-
(1997)
Nucl. Med. Biol
, vol.24
, pp. 187-191
-
-
Stone-Elander, S.1
Thorell, J.2
Eriksson, L.3
Fredholm, B.B.4
Ingvar, M.5
-
63
-
-
0343199237
-
Preparation and primary evaluation of [11C] CSC as a possible tracer for mapping adenosine A2A receptors by PET
-
Marian, T.; Boros, I.; Lengyel, Z.; Balkay, L.; Horvath, G.; Emri, M.; Sarkadi, E.; Szentmiklosi, A. J.; Fekete, I.; Tron, L. Preparation and primary evaluation of [11C]CSC as a possible tracer for mapping adenosine A2A receptors by PET. Appl. Radiat. Isot., 1999, 50, 887-893.
-
(1999)
Appl. Radiat. Isot
, vol.50
, pp. 887-893
-
-
Marian, T.1
Boros, I.2
Lengyel, Z.3
Balkay, L.4
Horvath, G.5
Emri, M.6
Sarkadi, E.7
Szentmiklosi, A.J.8
Fekete, I.9
Tron, L.10
-
64
-
-
0035889674
-
Evaluation of [4-O-methyl-(11)C]KW-6002 as a potential PET ligand for mapping central adenosine A(2A) receptors in rats
-
Hirani, E.; Gillies, J.; Karasawa, A.; Shimada, J.; Kase, H.; Opacka-Juffry, J.; Osman, S.; Luthra, S. K.; Hume, S. P.; Brooks, D. J. Evaluation of [4-O-methyl-(11)C]KW-6002 as a potential PET ligand for mapping central adenosine A(2A) receptors in rats. Synapse, 2001, 42, 164-176.
-
(2001)
Synapse
, vol.42
, pp. 164-176
-
-
Hirani, E.1
Gillies, J.2
Karasawa, A.3
Shimada, J.4
Kase, H.5
Opacka-Juffry, J.6
Osman, S.7
Luthra, S.K.8
Hume, S.P.9
Brooks, D.J.10
-
65
-
-
3042800189
-
Improved synthesis of [11C]SA4503, [11C]MPDX and [11C]TMSX by use of [11C]methyl triflate
-
Kawamura, K.; Ishiwata, K. Improved synthesis of [11C]SA4503, [11C]MPDX and [11C]TMSX by use of [11C]methyl triflate. Ann. Nucl. Med., 2004, 18, 165-168.
-
(2004)
Ann. Nucl. Med
, vol.18
, pp. 165-168
-
-
Kawamura, K.1
Ishiwata, K.2
-
66
-
-
0033759297
-
Carbon-11-labeled KF21213: A highly selective ligand for mapping CNS adenosine A2A receptors with positron emission tomography
-
Wang, W.; Ishiwata, K.; Nonaka, H.; Ishii, S.; Kiyosawa, M.; Shimada, J.; Suzuki, F.; Senda, M. Carbon-11-labeled KF21213: a highly selective ligand for mapping CNS adenosine A2A receptors with positron emission tomography. Nucl. Med. Biol., 2000, 27, 541-546.
-
(2000)
Nucl. Med. Biol
, vol.27
, pp. 541-546
-
-
Wang, W.1
Ishiwata, K.2
Nonaka, H.3
Ishii, S.4
Kiyosawa, M.5
Shimada, J.6
Suzuki, F.7
Senda, M.8
-
67
-
-
0027189806
-
Structure- activity relationships of 8-styrylxanthines as A2-selective adenosine antagonists
-
Jacobson, K. A.; Gallo-Rodriguez, C.; Melman, N.; Fischer, B.; Maillard, M.; van Bergen, A.; van Galen, P. J.; Karton, Y. Structure- activity relationships of 8-styrylxanthines as A2-selective adenosine antagonists. J. Med. Chem., 1993, 36, 1333-1342.
-
(1993)
J. Med. Chem
, vol.36
, pp. 1333-1342
-
-
Jacobson, K.A.1
Gallo-Rodriguez, C.2
Melman, N.3
Fischer, B.4
Maillard, M.5
Van Bergen, A.6
Van Galen, P.J.7
Karton, Y.8
-
68
-
-
0027141973
-
Photoisomerization of a potent and selective adenosine A2 antagonist, (E)-1,3- Dipropyl-8-(3,4-dimethoxystyryl)-7-methylxanthine
-
Nonaka, Y.; Shimada, J.; Nonaka, H.; Koike, N.; Aoki, N.; Kobayashi, H.; Kase, H.; Yamaguchi, K.; Suzuki, F. Photoisomerization of a potent and selective adenosine A2 antagonist, (E)-1,3- Dipropyl-8-(3,4-dimethoxystyryl)-7- methylxanthine. J. Med. Chem., 1993, 36, 3731-3733.
-
(1993)
J. Med. Chem
, vol.36
, pp. 3731-3733
-
-
Nonaka, Y.1
Shimada, J.2
Nonaka, H.3
Koike, N.4
Aoki, N.5
Kobayashi, H.6
Kase, H.7
Yamaguchi, K.8
Suzuki, F.9
-
69
-
-
0028176280
-
KF17837 ((E)-8-(3,4- dimethoxystyryl)-1,3-dipropyl-7-methylxanthine) a potent and selective adenosine A2 receptor antagonist
-
Nonaka, H.; Ichimura, M.; Takeda, M.; Nonaka, Y.; Shimada, J.; Suzuki, F.; Yamaguchi, K.; Kase, H. KF17837 ((E)-8-(3,4- dimethoxystyryl)-1,3-dipropyl- 7-methylxanthine) a potent and selective adenosine A2 receptor antagonist. Eur. J. Pharmacol., 1994, 267, 335-341.
-
(1994)
Eur. J. Pharmacol
, vol.267
, pp. 335-341
-
-
Nonaka, H.1
Ichimura, M.2
Takeda, M.3
Nonaka, Y.4
Shimada, J.5
Suzuki, F.6
Yamaguchi, K.7
Kase, H.8
-
70
-
-
0026690401
-
(E)-1,3- Dialkyl-7-methyl-8-(3,4,5-trimethoxy-styryl)xanthines: Potent and selective adenosine A2 antagonists
-
Shimada, J.; Suzuki, F.; Nonaka, H.; Ishii, A.; Ichikawa, S. (E)-1,3- Dialkyl-7-methyl-8-(3,4,5-trimethoxy-styryl)xanthines: Potent and selective adenosine A2 antagonists. J. Med. Chem., 1992, 35, 2342-2345.
-
(1992)
J. Med. Chem
, vol.35
, pp. 2342-2345
-
-
Shimada, J.1
Suzuki, F.2
Nonaka, H.3
Ishii, A.4
Ichikawa, S.5
-
71
-
-
0030610213
-
Myocardial adenosine A2a receptor imaging of rabbit by PET with [11C] KF17837
-
Ishiwata, K.; Sakiyama, Y.; Sakiyama, T.; Shimada, J.; Toyama, H.; Oda, K.; Suzuki, F.; Senda, M. Myocardial adenosine A2a receptor imaging of rabbit by PET with [11C]KF17837. Ann. Nucl. Med., 1997, 11, 219-225.
-
(1997)
Ann. Nucl. Med
, vol.11
, pp. 219-225
-
-
Ishiwata, K.1
Sakiyama, Y.2
Sakiyama, T.3
Shimada, J.4
Toyama, H.5
Oda, K.6
Suzuki, F.7
Senda, M.8
-
72
-
-
0031929827
-
Evaluation of carbon-11-labeled KF17837: A potential CNS adenosine A2a receptor ligand
-
Noguchi, J.; Ishiwata, K.; Wakabayashi, S.; Nariai, T.; Shumiya, S.; Ishii, S.; Toyama, H.; Endo, K.; Suzuki, F.; Senda, M. Evaluation of carbon-11-labeled KF17837: a potential CNS adenosine A2a receptor ligand. J. Nucl. Med., 1998, 39, 498-503.
-
(1998)
J. Nucl. Med
, vol.39
, pp. 498-503
-
-
Noguchi, J.1
Ishiwata, K.2
Wakabayashi, S.3
Nariai, T.4
Shumiya, S.5
Ishii, S.6
Toyama, H.7
Endo, K.8
Suzuki, F.9
Senda, M.10
-
73
-
-
0029670460
-
Evidence for high-affinity binding sites for the adenosine A2A receptor agonist [3H] CGS 21680 in the rat hippocampus and cerebral cortex that are different from striatal A2A receptors
-
Cunha, R. A.; Johansson, B.; Constantino, M. D.; Sebastiao, A. M.; Fredholm, B. B. Evidence for high-affinity binding sites for the adenosine A2A receptor agonist [3H] CGS 21680 in the rat hippocampus and cerebral cortex that are different from striatal A2A receptors. Naunyn Schmiedebergs Arch. Pharmacol., 1996, 353, 261-271.
-
(1996)
Naunyn Schmiedebergs Arch. Pharmacol
, vol.353
, pp. 261-271
-
-
Cunha, R.A.1
Johansson, B.2
Constantino, M.D.3
Sebastiao, A.M.4
Fredholm, B.B.5
-
74
-
-
0025328596
-
Autoradiographic evidence for G-protein coupled A2-receptors in rat neostriatum using [3H]-CGS 21680 as a ligand
-
Parkinson, F. E.; Fredholm, B. B. Autoradiographic evidence for G-protein coupled A2-receptors in rat neostriatum using [3H]-CGS 21680 as a ligand. Naunyn Schmiedebergs Arch. Pharmacol., 1990, 342, 85-89.
-
(1990)
Naunyn Schmiedebergs Arch. Pharmacol
, vol.342
, pp. 85-89
-
-
Parkinson, F.E.1
Fredholm, B.B.2
-
75
-
-
0025853692
-
Adenosine A2 receptors: Selective localization in the human basal ganglia and alterations with disease
-
Martinez-Mir, M. I.; Probst, A.; Palacios, J. M. Adenosine A2 receptors: selective localization in the human basal ganglia and alterations with disease. Neuroscience, 1991, 42, 697-706.
-
(1991)
Neuroscience
, vol.42
, pp. 697-706
-
-
Martinez-Mir, M.I.1
Probst, A.2
Palacios, J.M.3
-
76
-
-
0023413016
-
The distribution of adenosine a1 receptors and 5'-nucleotidase in the brain of some commonly used experimental animals
-
Fastbom, J.; Pazos, A.; Palacios, J. M. The distribution of adenosine a1 receptors and 5'-nucleotidase in the brain of some commonly used experimental animals. Neuroscience, 1987, 22, 813-826.
-
(1987)
Neuroscience
, vol.22
, pp. 813-826
-
-
Fastbom, J.1
Pazos, A.2
Palacios, J.M.3
-
77
-
-
0033776713
-
Evaluation of iodinated and brominated [11C]styrylxanthine derivatives as in vivo radioligands mapping adenosine A2A receptor in the central nervous system
-
Ishiwata, K.; Shimada, J.; Wang, W. F.; Harakawa, H.; Ishii, S.; Kiyosawa, M.; Suzuki, F.; Senda, M. Evaluation of iodinated and brominated [11C]styrylxanthine derivatives as in vivo radioligands mapping adenosine A2A receptor in the central nervous system. Ann. Nucl. Med., 2000, 14, 247-253.
-
(2000)
Ann. Nucl. Med
, vol.14
, pp. 247-253
-
-
Ishiwata, K.1
Shimada, J.2
Wang, W.F.3
Harakawa, H.4
Ishii, S.5
Kiyosawa, M.6
Suzuki, F.7
Senda, M.8
-
78
-
-
0034115544
-
Further characterization of a CNS adenosine A2a receptor ligand [11C] KF18446 with in vitro autoradiography and in vivo tissue uptake
-
Ishiwata, K.; Ogi, N.; Shimada, J.; Nonaka, H.; Tanaka, A.; Suzuki, F.; Senda, M. Further characterization of a CNS adenosine A2a receptor ligand [11C] KF18446 with in vitro autoradiography and in vivo tissue uptake. Ann. Nucl. Med., 2000, 14, 81-89.
-
(2000)
Ann. Nucl. Med
, vol.14
, pp. 81-89
-
-
Ishiwata, K.1
Ogi, N.2
Shimada, J.3
Nonaka, H.4
Tanaka, A.5
Suzuki, F.6
Senda, M.7
-
79
-
-
0034479434
-
Search for PET probes for imaging the globus pallidus studied with rat brainex vivo autoradiography
-
Ishiwata, K.; Ogi, N.; Shimada, J.; Wang, W.; Ishii, K.; Tanaka, A.; Suzuki, F.; Senda, M. Search for PET probes for imaging the globus pallidus studied with rat brainex vivo autoradiography. Ann. Nucl. Med., 2000, 14, 461-466.
-
(2000)
Ann. Nucl. Med
, vol.14
, pp. 461-466
-
-
Ishiwata, K.1
Ogi, N.2
Shimada, J.3
Wang, W.4
Ishii, K.5
Tanaka, A.6
Suzuki, F.7
Senda, M.8
-
80
-
-
0038268673
-
Preclinical studies on [11C] TMSX for mapping adenosine A2A receptors by positron emission tomography
-
Ishiwata, K.; Wang, W. F.; Kimura, Y.; Kawamura, K.; Ishii, K. Preclinical studies on [11C]TMSX for mapping adenosine A2A receptors by positron emission tomography. Ann. Nucl. Med., 2003, 17, 205-211.
-
(2003)
Ann. Nucl. Med
, vol.17
, pp. 205-211
-
-
Ishiwata, K.1
Wang, W.F.2
Kimura, Y.3
Kawamura, K.4
Ishii, K.5
-
81
-
-
0034676322
-
Design radiosynthesis, and biodistribution of a new potent and selective ligand for in vivo imaging of the adenosine A(2A) receptor system using positron emission tomography
-
Todde, S.; Moresco, R. M.; Simonelli, P.; Baraldi, P. G.; Cacciari, B.; Spalluto, G.; Varani, K.; Monopoli, A.; Matarrese, M.; Carpinelli, A.; Magni, F.; Kienle, M. G.; Fazio, F. Design, radiosynthesis, and biodistribution of a new potent and selective ligand for in vivo imaging of the adenosine A(2A) receptor system using positron emission tomography. J. Med. Chem., 2000, 43, 4359-4362.
-
(2000)
J. Med. Chem
, vol.43
, pp. 4359-4362
-
-
Todde, S.1
Moresco, R.M.2
Simonelli, P.3
Baraldi, P.G.4
Cacciari, B.5
Spalluto, G.6
Varani, K.7
Monopoli, A.8
Matarrese, M.9
Carpinelli, A.10
Magni, F.11
Kienle, M.G.12
Fazio, F.13
-
82
-
-
77957603165
-
Synthesis and evaluation of 1,2,4- triazolo[1,5-c]pyrimidine derivatives as A2A receptor-selective antagonists
-
Shinkre, B. A.; Kumar, T. S.; Gao, Z. G.; Deflorian, F.; Jacobson, K. A.; Trenkle, W. C. Synthesis and evaluation of 1,2,4- triazolo[1,5-c]pyrimidine derivatives as A2A receptor-selective antagonists. Bioorg. Med. Chem. Lett., 2010, 20, 5690-5694.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 5690-5694
-
-
Shinkre, B.A.1
Kumar, T.S.2
Gao, Z.G.3
Deflorian, F.4
Jacobson, K.A.5
Trenkle, W.C.6
-
83
-
-
79955483785
-
Molecular probes for the A2A adenosine receptor based on a pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine scaffold
-
Kumar, T. S.; Mishra, S.; Deflorian, F.; Yoo, L. S.; Phan, K.; Kecskes, M.; Szabo, A.; Shinkre, B.; Gao, Z. G.; Trenkle, W.; Jacobson, K. A. Molecular probes for the A2A adenosine receptor based on a pyrazolo[4,3-e][1,2,4] triazolo[1,5-c]pyrimidin-5-amine scaffold. Bioorg. Med. Chem. Lett., 2011, 21, 2740-2745.
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, pp. 2740-2745
-
-
Kumar, T.S.1
Mishra, S.2
Deflorian, F.3
Yoo, L.S.4
Phan, K.5
Kecskes, M.6
Szabo, A.7
Shinkre, B.8
Gao, Z.G.9
Trenkle, W.10
Jacobson, K.A.11
-
84
-
-
0037011899
-
7-Substituted 5- amino-2-(2-furyl)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c] pyrimidines as A2A adenosine receptor antagonists: A study on the importance of modifications at the side chain on the activity and solubility
-
Baraldi, P. G.; Cacciari, B.; Romagnoli, R.; Spalluto, G.; Monopoli, A.; Ongini, E.; Varani, K.; Borea, P. A. 7-Substituted 5- amino-2-(2-furyl) pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as A2A adenosine receptor antagonists: a study on the importance of modifications at the side chain on the activity and solubility. J. Med. Chem., 2002, 45, 115-126.
-
(2002)
J. Med. Chem
, vol.45
, pp. 115-126
-
-
Baraldi, P.G.1
Cacciari, B.2
Romagnoli, R.3
Spalluto, G.4
Monopoli, A.5
Ongini, E.6
Varani, K.7
Borea, P.A.8
-
85
-
-
17844371752
-
In vivo imaging of adenosine A2A receptors in rat and primate brain using [11C]SCH442416
-
Moresco, R. M.; Todde, S.; Belloli, S.; Simonelli, P.; Panzacchi, A.; Rigamonti, M.; Galli-Kienle, M.; Fazio, F. In vivo imaging of adenosine A2A receptors in rat and primate brain using [11C]SCH442416. Eur. J. Nucl. Med. Mol. Imaging, 2005, 32, 405-413.
-
(2005)
Eur. J. Nucl. Med. Mol. Imaging
, vol.32
, pp. 405-413
-
-
Moresco, R.M.1
Todde, S.2
Belloli, S.3
Simonelli, P.4
Panzacchi, A.5
Rigamonti, M.6
Galli-Kienle, M.7
Fazio, F.8
-
86
-
-
2442595210
-
Increased adenosine A2A receptors in the brain of Parkinson's disease patients with dyskinesias
-
Calon, F.; Dridi, M.; Hornykiewicz, O.; Bedard, P. J.; Rajput, A. H.; Di Paolo, T. Increased adenosine A2A receptors in the brain of Parkinson's disease patients with dyskinesias. Brain, 2004, 127, 1075-1084.
-
(2004)
Brain
, vol.127
, pp. 1075-1084
-
-
Calon, F.1
Dridi, M.2
Hornykiewicz, O.3
Bedard, P.J.4
Rajput, A.H.5
Di Paolo, T.6
-
87
-
-
46749156971
-
Brain adenosine A2A receptor occupancy by a novel A1/A2A receptor antagonist, ASP5854, in rhesus monkeys: Relationship to anticataleptic effect
-
Mihara, T.; Noda, A.; Arai, H.; Mihara, K.; Iwashita, A.; Murakami, Y.; Matsuya, T.; Miyoshi, S.; Nishimura, S.; Matsuoka, N. Brain adenosine A2A receptor occupancy by a novel A1/A2A receptor antagonist, ASP5854, in rhesus monkeys: relationship to anticataleptic effect. J. Nucl. Med., 2008, 49, 1183-1188.
-
(2008)
J. Nucl. Med
, vol.49
, pp. 1183-1188
-
-
Mihara, T.1
Noda, A.2
Arai, H.3
Mihara, K.4
Iwashita, A.5
Murakami, Y.6
Matsuya, T.7
Miyoshi, S.8
Nishimura, S.9
Matsuoka, N.10
-
88
-
-
84863687148
-
A2A receptor antagonism and dyskinesia in Parkinson's disease
-
Morelli, M.; Blandini, F.; Simola, N.; Hauser, R. A. A2A Receptor Antagonism and Dyskinesia in Parkinson's Disease. Parkinson's Disease, 2012, 2012, 8.
-
(2012)
Parkinson's Disease
, vol.2012
, pp. 8
-
-
Morelli, M.1
Blandini, F.2
Simola, N.3
Hauser, R.A.4
-
89
-
-
0025833464
-
Caffeine analogs: Structure-activity relationships at adenosine receptors
-
Daly, J. W.; Hide, I.; Muller, C. E.; Shamim, M. Caffeine Analogs: Structure-Activity Relationships at Adenosine Receptors. Pharmacology, 1991, 42, 309-321.
-
(1991)
Pharmacology
, vol.42
, pp. 309-321
-
-
Daly, J.W.1
Hide, I.2
Muller, C.E.3
Shamim, M.4
-
90
-
-
0031463493
-
Synthesis and structure-activity relationships of 3,7-dimethyl-1- propargylxanthine derivatives, A2A-selective adenosine receptor antagonists
-
Muller, C. E.; Geis, U.; Hipp, J.; Schobert, U.; Frobenius, W.; Pawlowski, M.; Suzuki, F.; Sandoval-Ramirez, J. Synthesis and structure-activity relationships of 3,7-dimethyl-1-propargylxanthine derivatives, A2A-selective adenosine receptor antagonists. J. Med. Chem., 1997, 40, 4396-4405.
-
(1997)
J. Med. Chem
, vol.40
, pp. 4396-4405
-
-
Muller, C.E.1
Geis, U.2
Hipp, J.3
Schobert, U.4
Frobenius, W.5
Pawlowski, M.6
Suzuki, F.7
Sandoval-Ramirez, J.8
-
91
-
-
0345698933
-
8-(Sulfostyryl)xanthines: Water-soluble A2A-selective adenosine receptor antagonists
-
Muller, C. E.; Sandoval-Ramirez, J.; Schobert, U.; Geis, U.; Frobenius, W.; Klotz, K. N. 8-(Sulfostyryl)xanthines: water-soluble A2A-selective adenosine receptor antagonists. Bioorg. Med. Chem., 1998, 6, 707-719.
-
(1998)
Bioorg. Med. Chem
, vol.6
, pp. 707-719
-
-
Muller, C.E.1
Sandoval-Ramirez, J.2
Schobert, U.3
Geis, U.4
Frobenius, W.5
Klotz, K.N.6
-
92
-
-
34248355605
-
Blocking striatal adenosine A2A receptors: A new strategy for basal ganglia disorders
-
Muller, C. E.; Ferre, S. Blocking striatal adenosine A2A receptors: a new strategy for basal ganglia disorders. Recent. Pat. CNS Drug Discov., 2007, 2, 1-21.
-
(2007)
Recent. Pat. CNS Drug Discov
, vol.2
, pp. 1-21
-
-
Muller, C.E.1
Ferre, S.2
-
93
-
-
70349303799
-
Recent developments in adenosine A2A receptor ligands
-
Cristalli, G.; Muller, C. E.; Volpini, R. Recent developments in adenosine A2A receptor ligands. Handb. Exp. Pharmacol., 2009, 193, 59-98.
-
(2009)
Handb. Exp. Pharmacol
, vol.193
, pp. 59-98
-
-
Cristalli, G.1
Muller, C.E.2
Volpini, R.3
-
94
-
-
0037717165
-
Impact of the aryl substituent kind and distance from pyrimido[2,1- f]purindiones on the adenosine receptor selectivity and antagonistic properties
-
Drabczynska, A.; Schumacher, B.; Muller, C. E.; Karolak-Wojciechowska, J.; Michalak, B.; Pekala, E.; Kiec-Kononowicz, K. Impact of the aryl substituent kind and distance from pyrimido[2,1- f]purindiones on the adenosine receptor selectivity and antagonistic properties. Eur. J. Med. Chem., 2003, 38, 397-402.
-
(2003)
Eur. J. Med. Chem
, vol.38
, pp. 397-402
-
-
Drabczynska, A.1
Schumacher, B.2
Muller, C.E.3
Karolak-Wojciechowska, J.4
Michalak, B.5
Pekala, E.6
Kiec-Kononowicz, K.7
-
95
-
-
33748648816
-
Improving potency, selectivity, and water solubility of adenosine A1 receptor antagonists: Xanthines modified at position 3 and related pyrimido[1,2,3-cd]purinediones
-
Weyler, S.; Fulle, F.; Diekmann, M.; Schumacher, B.; Hinz, S.; Klotz, K. N.; Muller, C. E. Improving potency, selectivity, and water solubility of adenosine A1 receptor antagonists: xanthines modified at position 3 and related pyrimido[1,2,3-cd]purinediones. ChemMedChem, 2006, 1, 891-902.
-
(2006)
ChemMedChem
, vol.1
, pp. 891-902
-
-
Weyler, S.1
Fulle, F.2
Diekmann, M.3
Schumacher, B.4
Hinz, S.5
Klotz, K.N.6
Muller, C.E.7
-
96
-
-
0038265864
-
Medicinal chemistry of adenosine A3 receptor ligands
-
Muller, C. E. Medicinal chemistry of adenosine A3 receptor ligands. Curr. Top. Med. Chem., 2003, 3, 445-462.
-
(2003)
Curr. Top. Med. Chem
, vol.3
, pp. 445-462
-
-
Muller, C.E.1
-
97
-
-
33644756543
-
Synthesis and pharmacology of pyrido[2,3- d]pyrimidinediones bearing polar substituents as adenosine receptor antagonists
-
Bulicz, J.; Bertarelli, D. C.; Baumert, D.; Fulle, F.; Muller, C. E.; Heber, D. Synthesis and pharmacology of pyrido[2,3- d]pyrimidinediones bearing polar substituents as adenosine receptor antagonists. Bioorg. Med. Chem., 2006, 14, 2837-2849.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 2837-2849
-
-
Bulicz, J.1
Bertarelli, D.C.2
Baumert, D.3
Fulle, F.4
Muller, C.E.5
Heber, D.6
-
98
-
-
27444442267
-
2-n-Butyl-9-methyl-8- [1,2,3]triazol-2-yl-9H-purin-6-ylamine and analogues as A2A adenosine receptor antagonists. Design, synthesis, and pharmacological characterization
-
Minetti, P.; Tinti, M. O.; Carminati, P.; Castorina, M.; Di Cesare, M. A.; Di Serio, S.; Gallo, G.; Ghirardi, O.; Giorgi, F.; Giorgi, L.; Piersanti, G.; Bartoccini, F.; Tarzia, G. 2-n-Butyl-9-methyl-8- [1,2,3]triazol-2-yl-9H- purin-6-ylamine and analogues as A2A adenosine receptor antagonists. Design, synthesis, and pharmacological characterization. J. Med. Chem., 2005, 48, 6887-6896.
-
(2005)
J. Med. Chem
, vol.48
, pp. 6887-6896
-
-
Minetti, P.1
Tinti, M.O.2
Carminati, P.3
Castorina, M.4
Di Cesare, M.A.5
Di Serio, S.6
Gallo, G.7
Ghirardi, O.8
Giorgi, F.9
Giorgi, L.10
Piersanti, G.11
Bartoccini, F.12
Tarzia, G.13
-
99
-
-
0027179838
-
Synthesis of imidazo[1,2-c]pyrazolo[4,3-e]pyrimidines, pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines and 1,2,4-triazolo [5,1-i]purines: New potent adenosine A2 receptor antagonists
-
Gatta, F.; Del Giudice, M.; Borioni, A.; Borea, P.; Dionisotti, S.; Ongini, E. Synthesis of imidazo[1,2-c]pyrazolo[4,3-e]pyrimidines, pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines and 1,2,4-triazolo [5,1-i]purines: new potent adenosine A2 receptor antagonists. Eur. J. Med. Chem., 1993, 28, 569-576.
-
(1993)
Eur. J. Med. Chem
, vol.28
, pp. 569-576
-
-
Gatta, F.1
Del Giudice, M.2
Borioni, A.3
Borea, P.4
Dionisotti, S.5
Ongini, E.6
-
100
-
-
0032482371
-
Design synthesis, and biological evaluation of a second generation of pyrazolo[4,3-e]- 1,2,4-triazolo[1,5-c]pyrimidines as potent and selective A2A adenosine receptor antagonists
-
Baraldi, P. G.; Cacciari, B.; Spalluto, G.; Bergonzoni, M.; Dionisotti, S.; Ongini, E.; Varani, K.; Borea, P. A. Design, synthesis, and biological evaluation of a second generation of pyrazolo[4,3-e]- 1,2,4-triazolo[1,5-c] pyrimidines as potent and selective A2A adenosine receptor antagonists. J. Med. Chem., 1998, 41, 2126-2133.
-
(1998)
J. Med. Chem
, vol.41
, pp. 2126-2133
-
-
Baraldi, P.G.1
Cacciari, B.2
Spalluto, G.3
Bergonzoni, M.4
Dionisotti, S.5
Ongini, E.6
Varani, K.7
Borea, P.A.8
-
101
-
-
0030004579
-
Pyrazolo[4,3- e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives: Potent and selective A(2A) adenosine antagonists
-
Baraldi, P. G.; Cacciari, B.; Spalluto, G.; Pineda de las Infantas y Villatoro,M.J.; Zocchi, C.; Dionisotti, S.; Ongini, E. Pyrazolo[4,3- e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives: potent and selective A(2A) adenosine antagonists. J. Med. Chem., 1996, 39, 1164-1171.
-
(1996)
J. Med. Chem
, vol.39
, pp. 1164-1171
-
-
Baraldi, P.G.1
Cacciari, B.2
Spalluto, G.3
Pineda De Las Infantas Y Villatoro, M.J.4
Zocchi, C.5
Dionisotti, S.6
Ongini, E.7
-
102
-
-
33846903864
-
Potent selective, and orally active adenosine A2A receptor antagonists: Arylpiperazine derivatives of pyrazolo[4,3-e]-1,2,4-triazolo[1,5- c]pyrimidines
-
Neustadt, B. R.; Hao, J.; Lindo, N.; Greenlee, W. J.; Stamford, A. W.; Tulshian, D.; Ongini, E.; Hunter, J.; Monopoli, A.; Bertorelli, R.; Foster, C.; Arik, L.; Lachowicz, J.; Ng, K.; Feng, K. Potent, selective, and orally active adenosine A2A receptor antagonists: Arylpiperazine derivatives of pyrazolo[4,3-e]-1,2,4-triazolo[1,5- c]pyrimidines. Bioorg. Med. Chem. Lett., 2007, 17, 1376-1380.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 1376-1380
-
-
Neustadt, B.R.1
Hao, J.2
Lindo, N.3
Greenlee, W.J.4
Stamford, A.W.5
Tulshian, D.6
Ongini, E.7
Hunter, J.8
Monopoli, A.9
Bertorelli, R.10
Foster, C.11
Arik, L.12
Lachowicz, J.13
Ng, K.14
Feng, K.15
-
103
-
-
33847063396
-
3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonists
-
Silverman, L. S.; Caldwell, J. P.; Greenlee, W. J.; Kiselgof, E.; Matasi, J. J.; Tulshian, D. B.; Arik, L.; Foster, C.; Bertorelli, R.; Monopoli, A.; Ongini, E. 3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonists. Bioorg. Med. Chem. Lett., 2007, 17, 1659-1662.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 1659-1662
-
-
Silverman, L.S.1
Caldwell, J.P.2
Greenlee, W.J.3
Kiselgof, E.4
Matasi, J.J.5
Tulshian, D.B.6
Arik, L.7
Foster, C.8
Bertorelli, R.9
Monopoli, A.10
Ongini, E.11
-
104
-
-
18844438125
-
Derivatives of 4,6-diamino-1,2-dihydro-2-phenyl- 1,2,4-triazolo[4,3-a] quinoxalin-2H-1-one: Potential antagonist ligands for imaging the A2A adenosine receptor by positron emission tomography (PET)
-
Holschbach, M. H.; Bier, D.; Wutz, W.; Sihver, W.; Schuller, M.; Olsson, R. A. Derivatives of 4,6-diamino-1,2-dihydro-2-phenyl- 1,2,4-triazolo[4,3-a] quinoxalin-2H-1-one: potential antagonist ligands for imaging the A2A adenosine receptor by positron emission tomography (PET). Eur. J. Med. Chem., 2005, 40, 421-437.
-
(2005)
Eur. J. Med. Chem
, vol.40
, pp. 421-437
-
-
Holschbach, M.H.1
Bier, D.2
Wutz, W.3
Sihver, W.4
Schuller, M.5
Olsson, R.A.6
-
105
-
-
33244498053
-
Synthesis and evaluation of 7-amino- 2-(2(3)-furyl)-5-phenylethylamino- oxazolo [5,4-d]pyrimidines as potential A2A adenosine receptor antagonists for positron emission tomography (PET)
-
Holschbach, M. H.; Bier, D.; Stusgen, S.; Wutz, W.; Sihver, W.; Coenen, H. H.; Olsson, R. A. Synthesis and evaluation of 7-amino- 2-(2(3)-furyl)-5- phenylethylamino-oxazolo [5,4-d]pyrimidines as potential A2A adenosine receptor antagonists for positron emission tomography (PET). Eur. J. Med. Chem., 2006, 41, 7-15.
-
(2006)
Eur. J. Med. Chem
, vol.41
, pp. 7-15
-
-
Holschbach, M.H.1
Bier, D.2
Stusgen, S.3
Wutz, W.4
Sihver, W.5
Coenen, H.H.6
Olsson, R.A.7
-
106
-
-
13944274827
-
The discovery and synthesis of novel adenosine receptor (A(2A)) antagonists
-
Matasi, J. J.; Caldwell, J. P.; Hao, J.; Neustadt, B.; Arik, L.; Foster, C. J.; Lachowicz, J.; Tulshian, D. B. The discovery and synthesis of novel adenosine receptor (A(2A)) antagonists. Bioorg. Med. Chem. Lett., 2005, 15, 1333-1336.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 1333-1336
-
-
Matasi, J.J.1
Caldwell, J.P.2
Hao, J.3
Neustadt, B.4
Arik, L.5
Foster, C.J.6
Lachowicz, J.7
Tulshian, D.B.8
-
107
-
-
4444302993
-
Studies on adenosine A2a receptor antagonists: Comparison of three core heterocycles
-
Vu, C. B.; Pan, D.; Peng, B.; Sha, L.; Kumaravel, G.; Jin, X.; Phadke, D.; Engber, T.; Huang, C.; Reilly, J.; Tam, S.; Petter, R. C. Studies on adenosine A2a receptor antagonists: comparison of three core heterocycles. Bioorg. Med. Chem. Lett., 2004, 14, 4831-4834.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 4831-4834
-
-
Vu, C.B.1
Pan, D.2
Peng, B.3
Sha, L.4
Kumaravel, G.5
Jin, X.6
Phadke, D.7
Engber, T.8
Huang, C.9
Reilly, J.10
Tam, S.11
Petter, R.C.12
-
108
-
-
25144524190
-
Synthesis of [1,2,4]triazolo[1,5- a]pyrazines as adenosine A2A receptor antagonists
-
Dowling, J. E.; Vessels, J. T.; Haque, S.; Chang, H. X.; van Vloten, K.; Kumaravel, G.; Engber, T.; Jin, X.; Phadke, D.; Wang, J.; Ayyub, E.; Petter, R. C. Synthesis of [1,2,4]triazolo[1,5- a]pyrazines as adenosine A2A receptor antagonists. Bioorg. Med. Chem. Lett., 2005, 15, 4809-4813.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 4809-4813
-
-
Dowling, J.E.1
Vessels, J.T.2
Haque, S.3
Chang, H.X.4
Van Vloten, K.5
Kumaravel, G.6
Engber, T.7
Jin, X.8
Phadke, D.9
Wang, J.10
Ayyub, E.11
Petter, R.C.12
-
109
-
-
22844440107
-
2-(2-Furanyl)-7- phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs: Highly potent, orally active, adenosine A2A antagonists. Part 1
-
Matasi, J. J.; Caldwell, J. P.; Zhang, H.; Fawzi, A.; Cohen-Williams, M. E.; Varty, G. B.; Tulshian, D. B. 2-(2-Furanyl)-7- phenyl[1,2,4]triazolo[1,5-c] pyrimidin-5-amine analogs: highly potent, orally active, adenosine A2A antagonists. Part 1. Bioorg. Med. Chem. Lett., 2005, 15, 3670-3674.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 3670-3674
-
-
Matasi, J.J.1
Caldwell, J.P.2
Zhang, H.3
Fawzi, A.4
Cohen-Williams, M.E.5
Varty, G.B.6
Tulshian, D.B.7
-
110
-
-
22844437672
-
2-(2- Furanyl)-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amine analogs as adenosine A2A antagonists: The successful reduction of hERG activity. Part 2
-
Matasi, J. J.; Caldwell, J. P.; Zhang, H.; Fawzi, A.; Higgins, G. A.; Cohen-Williams, M. E.; Varty, G. B.; Tulshian, D. B. 2-(2- Furanyl)-7-phenyl[1, 2,4]triazolo[1,5-c]pyrimidin-5-amine analogs as adenosine A2A antagonists: the successful reduction of hERG activity. Part 2. Bioorg. Med. Chem. Lett., 2005, 15, 3675-3678.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 3675-3678
-
-
Matasi, J.J.1
Caldwell, J.P.2
Zhang, H.3
Fawzi, A.4
Higgins, G.A.5
Cohen-Williams, M.E.6
Varty, G.B.7
Tulshian, D.B.8
-
111
-
-
3843123315
-
Piperazine derivatives of [1,2,4]triazolo[1,5-a][1,3,5]triazine as potent and selective adenosine A2a receptor antagonists
-
Vu, C. B.; Peng, B.; Kumaravel, G.; Smits, G.; Jin, X.; Phadke, D.; Engber, T.; Huang, C.; Reilly, J.; Tam, S.; Grant, D.; Hetu, G.; Chen, L.; Zhang, J.; Petter, R. C. Piperazine derivatives of [1,2,4]triazolo[1,5-a][1,3,5] triazine as potent and selective adenosine A2a receptor antagonists. J. Med. Chem., 2004, 47, 4291-4299.
-
(2004)
J. Med. Chem
, vol.47
, pp. 4291-4299
-
-
Vu, C.B.1
Peng, B.2
Kumaravel, G.3
Smits, G.4
Jin, X.5
Phadke, D.6
Engber, T.7
Huang, C.8
Reilly, J.9
Tam, S.10
Grant, D.11
Hetu, G.12
Chen, L.13
Zhang, J.14
Petter, R.C.15
-
112
-
-
20144385978
-
Novel diamino derivatives of [1,2,4]triazolo[1,5-a][1,3,5]triazine as potent and selective adenosine A2a receptor antagonists
-
Vu, C. B.; Pan, D.; Peng, B.; Kumaravel, G.; Smits, G.; Jin, X.; Phadke, D.; Engber, T.; Huang, C.; Reilly, J.; Tam, S.; Grant, D.; Hetu, G.; Petter, R. C. Novel diamino derivatives of [1,2,4]triazolo[1,5-a][1,3,5]triazine as potent and selective adenosine A2a receptor antagonists. J. Med. Chem., 2005, 48, 2009-2018.
-
(2005)
J. Med. Chem
, vol.48
, pp. 2009-2018
-
-
Vu, C.B.1
Pan, D.2
Peng, B.3
Kumaravel, G.4
Smits, G.5
Jin, X.6
Phadke, D.7
Engber, T.8
Huang, C.9
Reilly, J.10
Tam, S.11
Grant, D.12
Hetu, G.13
Petter, R.C.14
-
113
-
-
9744276705
-
Novel bicyclic piperazine derivatives of triazolotriazine and triazolopyrimidines as highly potent and selective adenosine A2A receptor antagonists
-
Peng, H.; Kumaravel, G.; Yao, G.; Sha, L.; Wang, J.; Van Vlijmen, H.; Bohnert, T.; Huang, C.; Vu, C. B.; Ensinger, C. L.; Chang, H.; Engber, T. M.; Whalley, E. T.; Petter, R. C. Novel bicyclic piperazine derivatives of triazolotriazine and triazolopyrimidines as highly potent and selective adenosine A2A receptor antagonists. J. Med. Chem., 2004, 47, 6218-6229.
-
(2004)
J. Med. Chem
, vol.47
, pp. 6218-6229
-
-
Peng, H.1
Kumaravel, G.2
Yao, G.3
Sha, L.4
Wang, J.5
Van Vlijmen, H.6
Bohnert, T.7
Huang, C.8
Vu, C.B.9
Ensinger, C.L.10
Chang, H.11
Engber, T.M.12
Whalley, E.T.13
Petter, R.C.14
-
114
-
-
4444254922
-
Triamino derivatives of triazolotriazine and triazolopyrimidine as adenosine A2a receptor antagonists
-
Vu, C. B.; Shields, P.; Peng, B.; Kumaravel, G.; Jin, X.; Phadke, D.; Wang, J.; Engber, T.; Ayyub, E.; Petter, R. C. Triamino derivatives of triazolotriazine and triazolopyrimidine as adenosine A2a receptor antagonists. Bioorg. Med. Chem. Lett., 2004, 14, 4835-4838.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 4835-4838
-
-
Vu, C.B.1
Shields, P.2
Peng, B.3
Kumaravel, G.4
Jin, X.5
Phadke, D.6
Wang, J.7
Engber, T.8
Ayyub, E.9
Petter, R.C.10
-
115
-
-
56749103466
-
The 2.6 angstrom crystal structure of a human A2A adenosine receptor bound to an antagonist
-
Jaakola, V. P.; Griffith, M. T.; Hanson, M. A.; Cherezov, V.; Chien, E. Y.; Lane, J. R.; Ijzerman, A. P.; Stevens, R. C. The 2.6 angstrom crystal structure of a human A2A adenosine receptor bound to an antagonist. Science, 2008, 322, 1211-1217.
-
(2008)
Science
, vol.322
, pp. 1211-1217
-
-
Jaakola, V.P.1
Griffith, M.T.2
Hanson, M.A.3
Cherezov, V.4
Chien, E.Y.5
Lane, J.R.6
Ijzerman, A.P.7
Stevens, R.C.8
-
116
-
-
47349097287
-
Computational studies of the binding modes of A 2A adenosine receptor antagonists
-
Ye, Y.; Wei, J.; Dai, X.; Gao, Q. Computational studies of the binding modes of A 2A adenosine receptor antagonists. Amino Acids, 2008, 35, 389-396.
-
(2008)
Amino Acids
, vol.35
, pp. 389-396
-
-
Ye, Y.1
Wei, J.2
Dai, X.3
Gao, Q.4
-
117
-
-
0029043501
-
Site-directed mutagenesis identifies residues involved in ligand recognition in the human A2a adenosine receptor
-
Kim, J.; Wess, J.; van Rhee, A. M.; Schoneberg, T.; Jacobson, K. A. Site-directed mutagenesis identifies residues involved in ligand recognition in the human A2a adenosine receptor. J. Biol. Chem., 1995, 270, 13987-13997.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 13987-13997
-
-
Kim, J.1
Wess, J.2
Van Rhee, A.M.3
Schoneberg, T.4
Jacobson, K.A.5
-
118
-
-
58549113972
-
Potent and selective adenosine A2A receptor antagonists: 1,2,4-Triazolo[1,5- c]pyrimidines
-
Neustadt, B. R.; Liu, H.; Hao, J.; Greenlee, W. J.; Stamford, A. W.; Foster, C.; Arik, L.; Lachowicz, J.; Zhang, H.; Bertorelli, R.; Fredduzzi, S.; Varty, G.; Cohen-Williams, M.; Ng, K. Potent and selective adenosine A2A receptor antagonists: 1,2,4-Triazolo[1,5- c]pyrimidines. Bioorg. Med. Chem. Lett., 2009, 19, 967-971.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 967-971
-
-
Neustadt, B.R.1
Liu, H.2
Hao, J.3
Greenlee, W.J.4
Stamford, A.W.5
Foster, C.6
Arik, L.7
Lachowicz, J.8
Zhang, H.9
Bertorelli, R.10
Fredduzzi, S.11
Varty, G.12
Cohen-Williams, M.13
Ng, K.14
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