Search Results - "Gawell, L"
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New Diarylmethylpiperazines as Potent and Selective Nonpeptidic δ Opioid Receptor Agonists with Increased In Vitro Metabolic Stability
Published in Journal of medicinal chemistry (19-10-2000)“…Nonpeptide δ opioid agonists are analgesics with a potentially improved side-effect and abuse liability profile, compared to classical opioids. Andrews…”
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N,N-Diethyl-4-(phenylpiperidin-4-ylidenemethyl)benzamide: A Novel, Exceptionally Selective, Potent δ Opioid Receptor Agonist with Oral Bioavailability and Its Analogues
Published in Journal of medicinal chemistry (19-10-2000)“…The design, synthesis, and pharmacological evaluation of a novel class of δ opioid receptor agonists, N,N-diethyl-4-(phenylpiperidin-4-ylidenemethyl)benzamide…”
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Binding of a specific 5-HT uptake inhibitor, [3H]norzimelidine, to rat brain homogenates
Published in European journal of pharmacology (21-05-1982)Get more information
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Synthesis of N, N-diethyl-4-[phenyl-(piperidin-4-ylidene)methyl]-[carboxy-14C]benzamide, a potent δ opioid receptor agonist
Published in Journal of labelled compounds & radiopharmaceuticals (01-02-2003)“…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
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
Published in Acta chemica Scandinavica (Copenhagen. 1989) (01-05-1989)“…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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Studies on orchidaceae alkaloids. XXXVII. Dendrowardine, a quaternary alkaloid from Dendrobium wardianum Wr
Published in Acta chemica Scandinavica (1973)Get more information
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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
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
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
Published in Progress in neuro-psychopharmacology & biological psychiatry (1988)“…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
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
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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