Literature DB >> 8891608

N3-phenacyluridine, a novel hypnotic compound, interacts with the benzodiazepine receptor.

T Kimura1, J Kuze, K Watanabe, S Kondo, I K Ho, I Yamamoto.   

Abstract

N3-Phenacyluridine (3-phenacyl-1-beta-D-ribofuranosyluracil) has potent sedative and hypnotic activities following intracerebroventricular injection in mice. To study the mechanism of action of N3-phenacyluridine, the interaction of this compound with the benzodiazepine receptor has been investigated. Results obtained showed that this compound inhibited specific binding of [3H]flunitrazepam to synaptic membranes of bovine cortex in a concentration-dependent fashion (IC50 = 129 microM). Scatchard analysis of [3H]flunitrazepam binding revealed that N3-phenacyluridine interacted with the ligand at the benzodiazepine receptor binding site in a competitive manner. Ro15-1788 (8-fluoro-3-carboethoxy-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5a ]1, 4-benzodiazepine), a benzodiazepine receptor antagonist, also inhibited the specific binding of [3H]flunitrazepam in the presence of the compound. The results suggest that the pharmacological activity of N3-phenacyluridine may be partially mediated through the benzodiazepine receptor.

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Year:  1996        PMID: 8891608     DOI: 10.1016/0014-2999(96)00434-7

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  1 in total

1.  A developmental cell-type switch in cortical interneurons leads to a selective defect in cortical oscillations.

Authors:  Naoki Takada; Hyun Jae Pi; Vitor H Sousa; Jack Waters; Gord Fishell; Adam Kepecs; Pavel Osten
Journal:  Nat Commun       Date:  2014-10-30       Impact factor: 14.919

  1 in total

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