Search Results - "Gawell, L"

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    Synthesis of N, N-diethyl-4-[phenyl-(piperidin-4-ylidene)methyl]-[carboxy-14C]benzamide, a potent δ opioid receptor agonist by Gawell, Lars

    “…The synthesis of carbon‐14 labelled N,N‐diethyl‐4‐[phenyl‐(piperidin‐4‐ylidene)methyl]‐benzamide is described. The radioisotope is introduced via an…”
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    Preventing Biomolecular Adsorption in Electrowetting-Based Biofluidic Chips by Yoon, Jeong-Yeol, Garrell, Robin L

    Published in Analytical chemistry (Washington) (01-10-2003)
    “…Electrowetting-on-dielectric (EWOD) is a new method for moving liquids in biofluidic chips through electrical modification of the surface hydrophobicity…”
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    Synthesis of 5-substituted 5-hydroxy-2-pyrrolidones, metabolites of the antipsychotic benzamide remoxipride by Gawell, L, Hagberg, C E, Högberg, T, Widman, M

    “…This paper describes the synthesis of 5-[(3-bromo-2,6-dimethoxybenzamido)-methyl]-5-hydroxy-2-pyrrolidon e (3) and its 1-ethyl analogue 2, two urinary…”
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    Some in vitro receptor binding properties of [3H]eticlopride, a novel substituted benzamide, selective for dopamine-D2 receptors in the rat brain by Hall, H, Köhler, C, Gawell, L

    Published in European journal of pharmacology (08-05-1985)
    “…The substituted benzamide compound eticlopride, (S)-(-)-5-chloro-3-ethyl-N-[(1-ethyl-2-pyrrolidinyl) methyl]-6-methoxysalicylamide hydrochloride (FLB 131), has…”
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    Regional in vivo binding of the substituted benzamide [3H]eticlopride in the rat brain: evidence for selective labelling of dopamine receptors by Köhler, C, Hall, H, Gawell, L

    Published in European journal of pharmacology (21-01-1986)
    “…The novel substituted benzamide eticlopride, (S)-(-)-5-chloro-3-ethyl-N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxy salicylamide hydrochloride (A38503; FLB…”
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    Raclopride, a new selective ligand for the dopamine-D2 receptors by Hall, H, Köhler, C, Gawell, L, Farde, L, Sedvall, G

    “…1. The use of raclopride, a new compound of the salicylamide series, as a ligand for the labelling of dopamine-D2 receptors in vitro and in vivo is described…”
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    Specific in vitro and in vivo binding of 3H-raclopride. A potent substituted benzamide drug with high affinity for dopamine D-2 receptors in the rat brain by Köhler, C, Hall, H, Ogren, S O, Gawell, L

    Published in Biochemical pharmacology (01-07-1985)
    “…The substituted benzamide drug raclopride, [((-)-(S)-3,5-dichloro-N-((1-ethyl-2-pyrrolidinyl) methyl)-6-methoxy-salicylamide tartrate; FLA 870(-); A40664] was…”
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    Stereoselective high-affinity binding of 3H-alaproclate to membranes from rat cerebral cortex by Ross, S B, Gawell, L, Hall, H

    Published in Pharmacology & toxicology (01-11-1987)
    “…The binding of 3H-alaproclate, a selective 5-hydroxytryptamine uptake inhibitor, to membranes prepared from the rat cerebral cortex was investigated by a…”
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