Search Results - "DE PAULIS, T"
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Sodium-dependent isomerization of dopamine D-2 receptors characterized using [125I]epidepride, a high-affinity substituted benzamide ligand
Published in The Journal of pharmacology and experimental therapeutics (01-03-1990)“…We have characterized the in vitro binding of a new ligand, [125I]epidepride, and used this substituted benzamide to assess the sensitivity of dopamine D-2…”
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2
Extrastriatal dopamine D2 receptors: distribution, pharmacological characterization and region-specific regulation by clozapine
Published in The Journal of pharmacology and experimental therapeutics (01-06-1992)“…The distribution of dopamine D2 receptors in the rat brain was determined by quantitative autoradiography of the binding of [125I]epidepride and the effects of…”
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3
Effect of Roasting on the Formation of Chlorogenic Acid Lactones in Coffee
Published in Journal of agricultural and food chemistry (09-03-2005)“…Of all plant constituents, coffee has one of the highest concentrations of chlorogenic acids. When roasting coffee, some of these are transformed into…”
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4
High Affinity Dopamine D2 Receptor Radioligands. 1. Regional Rat Brain Distribution of Iodinated Benzamides
Published in The Journal of nuclear medicine (1978) (01-08-1991)“…Five 125I-labeled substituted benzamides, which are close structural analogues of (S)-sulpiride, eticlopride, and isoremoxipride, were evaluated for their…”
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5
Chlorogenic Acids and Lactones in Regular and Water-Decaffeinated Arabica Coffees
Published in Journal of agricultural and food chemistry (25-01-2006)“…The market for decaffeinated coffees has been increasingly expanding over the years. Caffeine extraction may result in losses of other compounds such as…”
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6
High affinity dopamine D2 receptor radioligands. 2. [125I]epidepride, a potent and specific radioligand for the characterization of striatal and extrastriatal dopamine D2 receptors
Published in Life sciences (1973) (1991)“…Epidepride, (S)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-5-iodo-2,3-dimethoxybenzamide+ ++, the iodine analogue of isoremoxipride (FLB 457), was found to be a very…”
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7
Dosimetry of Iodine-123-Epidepride: A Dopamine D2 Receptor Ligand
Published in The Journal of nuclear medicine (1978) (01-07-1995)“…Substituted benzamides have been shown to have very high affinity and specificity for the dopamine D2 receptor. One of these is radiolabeled epidepride, an…”
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8
Antioxidant effects of dihydrocaffeic acid in human EA.hy926 endothelial cells
Published in The Journal of nutritional biochemistry (01-12-2004)“…Dihydrocaffeic acid (DHCA) is a metabolite of caffeic acid with potent antioxidant properties. Since DHCA has been detected in human plasma following coffee…”
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9
Quinides of roasted coffee enhance insulin action in conscious rats
Published in The Journal of nutrition (01-11-2003)“…Consumption of large amounts of coffee has been shown to decrease the incidence of type 2 diabetes. However, the specific compounds and mechanisms responsible…”
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10
Metabolism of zimelidine in rat, dog and man. Identification and synthesis of the principal metabolites
Published in Arzneimittel-Forschung (1981)“…Several metabolites of (Z)-3-(4-bromophenyl)-N,N-dimethyl-3-(3-pyridyl)allylamine (zimelidine) were isolated from urine of rat and dog after administration of…”
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11
Comprehensive analysis of major and minor chlorogenic acids and lactones in economically relevant Brazilian coffee cultivars
Published in Food chemistry (2008)“…Coffee is the most consumed beverage in the world and a significant source of phenolic compounds, particularly chlorogenic acids (CGA). During coffee roasting,…”
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12
Dicinnamoylquinides in roasted coffee inhibit the human adenosine transporter
Published in European journal of pharmacology (10-05-2002)“…Preliminary screening of a minor, non-xanthine constituent of roasted coffee, 3,4-diferuloyl-1,5-quinolactone (DIFEQ), showed inhibition of the adenosine…”
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13
4-Caffeoyl-1,5-quinide in roasted coffee inhibits [3H]naloxone binding and reverses anti-nociceptive effects of morphine in mice
Published in Psychopharmacologia (01-11-2004)“…Cinnamoylquinides are formed from the corresponding chlorogenic acids during coffee roasting. Instant coffee has been shown to displace binding of the mu…”
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14
Labeling of (S)-DES-4-amino-3-[125I]iodozacopride (DAIZAC), a high-affinity radioligand for the 5-HT-3 receptor
Published in Journal of labelled compounds & radiopharmaceuticals (01-11-1996)“…We have prepared (S)‐5‐chloro‐3‐[125I]iodo‐2‐methoxy‐N‐(1‐azabicyclo[2.2.2]oct‐3‐yl)‐benzamide ([125I]DAIZAC, [125I]‐3) as a radioligand for characterization…”
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15
On the topology of the norepinephrine transport carrier in rat hypothalamus. The site of action of tricyclic uptake inhibitors
Published in Molecular pharmacology (01-07-1978)Get more information
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16
M-100907 (Aventis)
Published in Current opinion in investigational drugs (London, England : 2000) (01-01-2001)“…M-100907 is a highly selective 5-HT2A antagonist that is being developed by Aventis Pharmaceuticals, formerly Hoechst Marion Roussel (HMR), for the potential…”
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17
Identification of extrastriatal dopamine D2 receptors in post mortem human brain with [125I]epidepride
Published in Brain research (23-04-1993)“…The regional distribution of striatal and extrastriatal dopamine D2 receptors in human brain was studied in vitro with (S)-N-[(1-ethyl-2-…”
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18
Solid state conformations and antidopaminergic effects of remoxipride hydrochloride and a closely related salicylamide, FLA 797, in relation to dopamine receptor models
Published in Molecular pharmacology (01-10-1986)“…The X-ray structures of two new 2,6-disubstituted benzamides, i.e., remoxipride hydrochloride monohydrate…”
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Anxiolytic-like effects of DAIZAC, a selective high-affinity 5-HT3 receptor antagonist, in the mouse elevated plus-maze
Published in Pharmacology, biochemistry and behavior (01-07-2001)Get full text
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20
Pharmacological characterization of morphine-6-sulfate and codeine-6-sulfate
Published in Brain research (18-09-1999)“…Morphine-6-sulfate (M6S) and codeine-6-sulfate (C6S) are mu-selective opiates which have been isolated from brain. M6S is an effective analgesic, with a…”
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