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PUBMED FOR HANDHELDS

Journal Abstract Search


136 related items for PubMed ID: 1675452

  • 1. R(-)2-fluoro-N-n-propylnorapomorphine: a very potent and D2-selective dopamine agonist.
    Baldessarini RJ, Kula NS, Gao Y, Campbell A, Neumeyer JL.
    Neuropharmacology; 1991 Jan; 30(1):97-9. PubMed ID: 1675452
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  • 4. Synthesis and dopamine receptor affinities of enantiomers of 2-substituted apomorphines and their N-n-propyl analogues.
    Gao YG, Baldessarini RJ, Kula NS, Neumeyer JL.
    J Med Chem; 1990 Jun; 33(6):1800-5. PubMed ID: 1971309
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  • 5. Stimulation of high-affinity adenosine A2 receptors decreases the affinity of dopamine D2 receptors in rat striatal membranes.
    Ferre S, von Euler G, Johansson B, Fredholm BB, Fuxe K.
    Proc Natl Acad Sci U S A; 1991 Aug 15; 88(16):7238-41. PubMed ID: 1678519
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  • 6. Synthesis and structural requirements of N-substituted norapomorphines for affinity and activity at dopamine D-1, D-2, and agonist receptor sites in rat brain.
    Gao YG, Ram VJ, Campbell A, Kula NS, Baldessarini RJ, Neumeyer JL.
    J Med Chem; 1990 Jan 15; 33(1):39-44. PubMed ID: 2136919
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  • 7. Inhibition of substantia nigra dopamine cell firing by R(-)-N-n-propylnorapomorphine: electrophysiological and autoradiographic studies after regional inactivation of dopamine receptors by microinjection of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline.
    Cox RF, Waszczak BL.
    Brain Res; 1993 Jun 04; 613(1):32-42. PubMed ID: 8102308
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  • 8. Synaptic concentration of dopamine in the mouse striatum in relationship to the kinetic properties of the dopamine receptors and uptake mechanism.
    Ross SB.
    J Neurochem; 1991 Jan 04; 56(1):22-9. PubMed ID: 1824780
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  • 9. Vanadate inhibits agonist binding to D2 dopamine receptor.
    Elazar Z, Fuchs S.
    J Mol Neurosci; 1991 Jan 04; 3(1):1-6. PubMed ID: 1679343
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  • 10. Characterization of normal and supersensitive dopamine receptors: effects of ergot drugs and neuropeptides.
    Fuxe K, Agnati LF, Köhler C, Kuonen D, Ogren SO, Andersson K, Hökfelt T.
    J Neural Transm; 1981 Jan 04; 51(1-2):3-37. PubMed ID: 7264628
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  • 11. Further characterization of structural requirements for agonists at the striatal dopamine D2 receptor and a comparison with those at the striatal dopamine D1 receptor. Studies with a series of monohydroxyaminotetralins on acetylcholine release from rat striatum.
    Seiler MP, Markstein R.
    Mol Pharmacol; 1984 Nov 04; 26(3):452-7. PubMed ID: 6238231
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  • 12. The benzazepine, SCH 23390, inhibits 3H-NPA binding in mouse brain in vivo.
    Andersen PH, Nielsen EB.
    Acta Pharmacol Toxicol (Copenh); 1986 Oct 04; 59(4):315-8. PubMed ID: 2948372
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  • 13. Heterogeneous distribution of dopamine D2 receptors within the rat striatum as revealed by autoradiography of [3H]N-n-propylnorapomorphine binding sites.
    Dubois A, Scatton B.
    Neurosci Lett; 1985 Jun 04; 57(1):7-12. PubMed ID: 3162114
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  • 16. 5-Oxygenated N-alkyl- and N,N-Dialkyl-2-amino-1-methyltetralins. Effects of structure and stereochemistry on dopamine-D2-receptor affinity.
    Grol CJ, Nordvall G, Johansson AM, Hacksell U.
    J Pharm Pharmacol; 1991 Jul 04; 43(7):481-5. PubMed ID: 1682460
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  • 17. Specific binding of [(11)C]raclopride and N-[(3)H]propyl-norapomorphine to dopamine receptors in living mouse striatum: occupancy by endogenous dopamine and guanosine triphosphate-free G protein.
    Cumming P, Wong DF, Gillings N, Hilton J, Scheffel U, Gjedde A.
    J Cereb Blood Flow Metab; 2002 May 04; 22(5):596-604. PubMed ID: 11973432
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  • 18. Correspondency between different affinity states and target size of the bovine striatal D2 dopamine receptor.
    Kuno T, Tanaka C.
    Biochem Biophys Res Commun; 1983 Nov 30; 117(1):65-70. PubMed ID: 6197972
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  • 19. Synthesis and dopamine receptor affinities of N-alkyl-11-hydroxy-2-methoxynoraporphines: N-alkyl substituents determine D1 versus D2 receptor selectivity.
    Si YG, Gardner MP, Tarazi FI, Baldessarini RJ, Neumeyer JL.
    J Med Chem; 2008 Feb 28; 51(4):983-7. PubMed ID: 18251489
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  • 20. Repeated D1 dopamine receptor agonist administration prevents the development of both D1 and D2 striatal receptor supersensitivity following denervation.
    Hu XT, White FJ.
    Synapse; 1992 Mar 28; 10(3):206-16. PubMed ID: 1532677
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