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Journal Abstract Search

360 related items for PubMed ID: 8730729

  • 1. Binding of the radioligand [3H]-SCH 58261, a new non-xanthine A2A adenosine receptor antagonist, to rat striatal membranes.
    Zocchi C, Ongini E, Ferrara S, Baraldi PG, Dionisotti S.
    Br J Pharmacol; 1996 Apr; 117(7):1381-6. PubMed ID: 8730729
    [Abstract] [Full Text] [Related]

  • 2. Characterization of human A2A adenosine receptors with the antagonist radioligand [3H]-SCH 58261.
    Dionisotti S, Ongini E, Zocchi C, Kull B, Arslan G, Fredholm BB.
    Br J Pharmacol; 1997 Jun; 121(3):353-60. PubMed ID: 9179373
    [Abstract] [Full Text] [Related]

  • 3. G protein coupling of CGS 21680 binding sites in the rat hippocampus and cortex is different from that of adenosine A1 and striatal A2A receptors.
    Cunha RA, Constantino MD, Ribeiro JA.
    Naunyn Schmiedebergs Arch Pharmacol; 1999 Apr; 359(4):295-302. PubMed ID: 10344528
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  • 4. 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 RA, Johansson B, Constantino MD, Sebastião AM, Fredholm BB.
    Naunyn Schmiedebergs Arch Pharmacol; 1996 Feb; 353(3):261-71. PubMed ID: 8692280
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  • 5. Binding of the novel nonxanthine A2A adenosine receptor antagonist [3H]SCH58261 to coronary artery membranes.
    Belardinelli L, Shryock JC, Ruble J, Monopoli A, Dionisotti S, Ongini E, Dennis DM, Baker SP.
    Circ Res; 1996 Dec; 79(6):1153-60. PubMed ID: 8943953
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  • 6. [3H]CGS 21680, a selective A2 adenosine receptor agonist directly labels A2 receptors in rat brain.
    Jarvis MF, Schulz R, Hutchison AJ, Do UH, Sills MA, Williams M.
    J Pharmacol Exp Ther; 1989 Dec; 251(3):888-93. PubMed ID: 2600819
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  • 8. Binding of [3H]KF17837S, a selective adenosine A2 receptor antagonist, to rat brain membranes.
    Nonaka H, Mori A, Ichimura M, Shindou T, Yanagawa K, Shimada J, Kase H.
    Mol Pharmacol; 1994 Nov; 46(5):817-22. PubMed ID: 7969067
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  • 10. Effects of adenosine receptor agonists and antagonists on audiogenic seizure-sensible DBA/2 mice.
    De Sarro G, De Sarro A, Di Paola ED, Bertorelli R.
    Eur J Pharmacol; 1999 Apr 29; 371(2-3):137-45. PubMed ID: 10357250
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  • 13. Species differences in brain adenosine A1 receptor pharmacology revealed by use of xanthine and pyrazolopyridine based antagonists.
    Maemoto T, Finlayson K, Olverman HJ, Akahane A, Horton RW, Butcher SP.
    Br J Pharmacol; 1997 Nov 29; 122(6):1202-8. PubMed ID: 9401787
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  • 14. The non-xanthine heterocyclic compound SCH 58261 is a new potent and selective A2a adenosine receptor antagonist.
    Zocchi C, Ongini E, Conti A, Monopoli A, Negretti A, Baraldi PG, Dionisotti S.
    J Pharmacol Exp Ther; 1996 Feb 29; 276(2):398-404. PubMed ID: 8632302
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  • 15. Characterization of the binding of a novel nonxanthine adenosine antagonist radioligand, [3H]CGS 15943, to multiple affinity states of the adenosine A1 receptor in the rat cortex.
    Jarvis MF, Williams M, Do UH, Sills MA.
    Mol Pharmacol; 1991 Jan 29; 39(1):49-54. PubMed ID: 1987452
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  • 17. Binding of [3H]MSX-2 (3-(3-hydroxypropyl)-7-methyl-8-(m-methoxystyryl)-1-propargylxanthine) to rat striatal membranes--a new, selective antagonist radioligand for A(2A) adenosine receptors.
    Müller CE, Maurinsh J, Sauer R.
    Eur J Pharm Sci; 2000 Jan 29; 10(4):259-65. PubMed ID: 10838015
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  • 18. Autoradiographic comparison of the potency of several structurally unrelated adenosine receptor antagonists at adenosine A1 and A(2A) receptors.
    Fredholm BB, Lindström K.
    Eur J Pharmacol; 1999 Sep 10; 380(2-3):197-202. PubMed ID: 10513579
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  • 19. [3H]-SCH 58261 labelling of functional A2A adenosine receptors in human neutrophil membranes.
    Varani K, Gessi S, Dionisotti S, Ongini E, Borea PA.
    Br J Pharmacol; 1998 Apr 10; 123(8):1723-31. PubMed ID: 9605581
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  • 20. Use of the triazolotriazine [3H]ZM 241385 as a radioligand at recombinant human A2B adenosine receptors.
    Ji XD, Jacobson KA.
    Drug Des Discov; 1999 Nov 10; 16(3):217-26. PubMed ID: 10624567
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