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Journal Abstract Search

142 related items for PubMed ID: 7932572

  • 1. Structure-activity relationship studies of N-sulfonyl analogs of cocaine: role of ionic interaction in cocaine binding.
    Kozikowski AP, Saiah MK, Bergmann JS, Johnson KM.
    J Med Chem; 1994 Sep 30; 37(20):3440-2. PubMed ID: 7932572
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  • 2. Isothiocyanate derivatives of cocaine: irreversible inhibition of ligand binding at the dopamine transporter.
    Boja JW, Rahman MA, Philip A, Lewin AH, Carroll FI, Kuhar MJ.
    Mol Pharmacol; 1991 Mar 30; 39(3):339-45. PubMed ID: 1826041
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  • 3. Halogenated mazindol analogs as potential inhibitors of the cocaine binding site at the dopamine transporter.
    Houlihan WJ, Boja JW, Parrino VA, Kopajtic TA, Kuhar MJ.
    J Med Chem; 1996 Dec 06; 39(25):4935-41. PubMed ID: 8960553
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  • 4. Chemistry and biology of the 2 beta-alkyl-3 beta-phenyl analogues of cocaine: subnanomolar affinity ligands that suggest a new pharmacophore model at the C-2 position.
    Kozikowski AP, Eddine Saiah MK, Johnson KM, Bergmann JS.
    J Med Chem; 1995 Aug 04; 38(16):3086-93. PubMed ID: 7636872
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  • 5. Modeling of the pH dependence of the binding of WIN 35,428 to the dopamine transporter in rat striatal membranes: is the bioactive form positively charged or neutral?
    Xu C, Reith ME.
    J Pharmacol Exp Ther; 1996 Sep 04; 278(3):1340-8. PubMed ID: 8819521
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  • 6. Relationships between the catechol substrate binding site and amphetamine, cocaine, and mazindol binding sites in a kinetic model of the striatal transporter of dopamine in vitro.
    Wayment H, Meiergerd SM, Schenk JO.
    J Neurochem; 1998 May 04; 70(5):1941-9. PubMed ID: 9572278
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  • 7. Cocaine displaces [3H]WIN 35,428 binding to dopamine uptake sites in vivo more rapidly than mazindol or GBR 12909.
    Pögün S, Scheffel U, Kuhar MJ.
    Eur J Pharmacol; 1991 Jun 06; 198(2-3):203-5. PubMed ID: 1864307
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  • 8. Translocation of dopamine and binding of 2 beta-carbomethoxy-3 beta-(4-fluorophenyl) tropane (WIN 35,428) measured under identical conditions in rat striatal synaptosomal preparations. Inhibition by various blockers.
    Xu C, Coffey LL, Reith ME.
    Biochem Pharmacol; 1995 Jan 31; 49(3):339-50. PubMed ID: 7857321
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  • 9. Novel 2-substituted cocaine analogs: binding properties at dopamine transport sites in rat striatum.
    Davies HM, Saikali E, Sexton T, Childers SR.
    Eur J Pharmacol; 1993 Jan 04; 244(1):93-7. PubMed ID: 8420793
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  • 13. Relationship between [3H]mazindol binding to dopamine uptake sites and [3H]dopamine uptake in rat striatum during aging.
    Shimizu I, Prasad C.
    J Neurochem; 1991 Feb 04; 56(2):575-9. PubMed ID: 1988557
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  • 14. Binding of the cocaine analog 2 beta-carbomethoxy-3 beta-(4-[125I]iodophenyl)tropane to serotonin and dopamine transporters: different ionic requirements for substrate and 2 beta-carbomethoxy-3 beta-(4-[125I]iodophenyl)tropane binding.
    Wall SC, Innis RB, Rudnick G.
    Mol Pharmacol; 1993 Feb 04; 43(2):264-70. PubMed ID: 8429827
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  • 15. WIN 35,428 and mazindol are mutually exclusive in binding to the cloned human dopamine transporter.
    Xu C, Reith ME.
    J Pharmacol Exp Ther; 1997 Aug 04; 282(2):920-7. PubMed ID: 9262359
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  • 20. Interaction between a hydroxypiperidine analogue of 4-(2-benzhydryloxy-ethyl)-1-(4-fluorobenzyl)piperidine and Aspartate 68 in the human dopamine transporter.
    Zhen J, Maiti S, Chen N, Dutta AK, Reith ME.
    Eur J Pharmacol; 2004 Dec 03; 506(1):17-26. PubMed ID: 15588620
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