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Journal Abstract Search

359 related items for PubMed ID: 2374150

  • 1. 4-Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants.
    Sarges R, Howard HR, Browne RG, Lebel LA, Seymour PA, Koe BK.
    J Med Chem; 1990 Aug; 33(8):2240-54. PubMed ID: 2374150
    [Abstract] [Full Text] [Related]

  • 2. [1,2,4]Triazolo[4,3-a]quinoxalin-4-amines: a new class of A1 receptor selective adenosine antagonists.
    Trivedi BK, Bruns RF.
    J Med Chem; 1988 May; 31(5):1011-4. PubMed ID: 3361571
    [Abstract] [Full Text] [Related]

  • 3. 7-Deaza-2-phenyladenines: structure-activity relationships of potent A1 selective adenosine receptor antagonists.
    Müller CE, Hide I, Daly JW, Rothenhäusler K, Eger K.
    J Med Chem; 1990 Oct; 33(10):2822-8. PubMed ID: 2213835
    [Abstract] [Full Text] [Related]

  • 4. Characterization of the A2 adenosine receptor labeled by [3H]NECA in rat striatal membranes.
    Bruns RF, Lu GH, Pugsley TA.
    Mol Pharmacol; 1986 Apr; 29(4):331-46. PubMed ID: 3010074
    [Abstract] [Full Text] [Related]

  • 5. [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
    [Abstract] [Full Text] [Related]

  • 6. Effects of the new A2 adenosine receptor antagonist 8FB-PTP, an 8 substituted pyrazolo-triazolo-pyrimidine, on in vitro functional models.
    Dionisotti S, Conti A, Sandoli D, Zocchi C, Gatta F, Ongini E.
    Br J Pharmacol; 1994 Jun; 112(2):659-65. PubMed ID: 8075885
    [Abstract] [Full Text] [Related]

  • 7. 1,2,4-Triazolo[1,5-a]quinoxaline derivatives: synthesis and biological evaluation as adenosine receptor antagonists.
    Catarzi D, Colotta V, Varano F, Filacchioni G, Martini C, Trincavelli L, Lucacchini A.
    Farmaco; 2004 Feb; 59(2):71-81. PubMed ID: 14871498
    [Abstract] [Full Text] [Related]

  • 8. 8-Polycycloalkyl-1,3-dipropylxanthines as potent and selective antagonists for A1-adenosine receptors.
    Shimada J, Suzuki F, Nonaka H, Ishii A.
    J Med Chem; 1992 Mar 06; 35(5):924-30. PubMed ID: 1548682
    [Abstract] [Full Text] [Related]

  • 9. Synthesis, ligand-receptor modeling studies and pharmacological evaluation of novel 4-modified-2-aryl-1,2,4-triazolo[4,3-a]quinoxalin-1-one derivatives as potent and selective human A3 adenosine receptor antagonists.
    Colotta V, Catarzi D, Varano F, Lenzi O, Filacchioni G, Martini C, Trincavelli L, Ciampi O, Traini C, Pugliese AM, Pedata F, Morizzo E, Moro S.
    Bioorg Med Chem; 2008 Jun 01; 16(11):6086-102. PubMed ID: 18468446
    [Abstract] [Full Text] [Related]

  • 10. 1H-imidazo[4,5-c]quinolin-4-amines: novel non-xanthine adenosine antagonists.
    van Galen PJ, Nissen P, van Wijngaarden I, IJzerman AP, Soudijn W.
    J Med Chem; 1991 Mar 01; 34(3):1202-6. PubMed ID: 2002461
    [Abstract] [Full Text] [Related]

  • 11. N6,9-disubstituted adenines: potent, selective antagonists at the A1 adenosine receptor.
    Thompson RD, Secunda S, Daly JW, Olsson RA.
    J Med Chem; 1991 Sep 01; 34(9):2877-82. PubMed ID: 1895305
    [Abstract] [Full Text] [Related]

  • 12. 1-substituted 4-[chloropyrazolyl][1,2,4]triazolo[4,3-a]quinoxalines: synthesis and structure-activity relationships of a new class of benzodiazepine and adenosine receptor ligands.
    Matuszczak B, Pekala E, Müller CE.
    Arch Pharm (Weinheim); 1998 May 01; 331(5):163-9. PubMed ID: 9691247
    [Abstract] [Full Text] [Related]

  • 13. Excitatory transmitter amino acid release from the ischemic rat cerebral cortex: effects of adenosine receptor agonists and antagonists.
    Simpson RE, O'Regan MH, Perkins LM, Phillis JW.
    J Neurochem; 1992 May 01; 58(5):1683-90. PubMed ID: 1348522
    [Abstract] [Full Text] [Related]

  • 14. N6-substituted N-alkyladenosine-5'-uronamides: bifunctional ligands having recognition groups for A1 and A2 adenosine receptors.
    Olsson RA, Kusachi S, Thompson RD, Ukena D, Padgett W, Daly JW.
    J Med Chem; 1986 Sep 01; 29(9):1683-9. PubMed ID: 3018244
    [Abstract] [Full Text] [Related]

  • 15. Synthesis and structure-activity relationships of 4-cycloalkylamino-1, 2, 4-triazolo[4, 3-a]quinoxalin-1- one derivatives as A1 and A3 adenosine receptor antagonists.
    Colotta V, Catarzi D, Varano F, Filacchioni G, Martini C, Trincavelli L, Lucacchini A, Colotta V.
    Arch Pharm (Weinheim); 2004 Jan 01; 337(1):35-41. PubMed ID: 14760626
    [Abstract] [Full Text] [Related]

  • 16. Novel 3-aralkyl-7-(amino-substituted)-1,2,3-triazolo[4,5-d]pyrimidines with high affinity toward A1 adenosine receptors.
    Betti L, Biagi G, Giannaccini G, Giorgi I, Livi O, Lucacchini A, Manera C, Scartoni V.
    J Med Chem; 1998 Feb 26; 41(5):668-73. PubMed ID: 9513594
    [Abstract] [Full Text] [Related]

  • 17. 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 26; 39(1):49-54. PubMed ID: 1987452
    [Abstract] [Full Text] [Related]

  • 18. Repeated treatment with adenosine A1 receptor agonist and antagonist modifies the anticonvulsant properties of CPPene.
    De Sarro G, Donato Di Paola E, Falconi U, Ferreri G, De Sarro A.
    Eur J Pharmacol; 1996 Dec 19; 317(2-3):239-45. PubMed ID: 8997606
    [Abstract] [Full Text] [Related]

  • 19. Trifunctional agents as a design strategy for tailoring ligand properties: irreversible inhibitors of A1 adenosine receptors.
    Boring DL, Ji XD, Zimmet J, Taylor KE, Stiles GL, Jacobson KA.
    Bioconjug Chem; 1991 Dec 19; 2(2):77-88. PubMed ID: 1868116
    [Abstract] [Full Text] [Related]

  • 20. N6-phenyladenosines: pronounced effect of phenyl substituents on affinity for A2 adenosine receptors.
    Kwatra MM, Leung E, Hosey MM, Green RD.
    J Med Chem; 1987 May 19; 30(5):954-6. PubMed ID: 3572985
    [Abstract] [Full Text] [Related]

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