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بريتازينيل

Bretazenil (Ro16-6028) is an imidazopyrrolobenzodiazepine anxiolytic drug which is derived from the benzodiazepine family, and was invented in 1988. It is most closely related in structure to the GABA antagonist flumazenil, although its effects are somewhat different. It is classified as a high-potency benzodiazepine due to its high affinity binding to benzodiazepine binding sites where it acts as a partial agonist. Its profile as a partial agonist and preclinical trial data suggests that it may have a reduced adverse effect profile. In particular bretazenil has been proposed to cause a less strong development of tolerance and withdrawal syndrome. Bretazenil differs from traditional 1,4-benzodiazepines by being a partial agonist and because it binds to α1, α2, α3, α4, α5 and α6 subunit containing GABAA receptor benzodiazepine receptor complexes. 1,4-benzodiazepines bind only to α1, α2, α3 and α5 GABAA benzodiazepine receptor complexes.

بريتازينيل molecular structure
بريتازينيل molecular structure diagram from the DrugsPRO substance library.

Classification

  • Chemical: Benzodiazepine
  • Psychoactive: Depressant

Effects

  • Sedation
  • Motor Impairment
  • Muscle Relaxation
  • Reduced Anxiety
  • Anxiety Suppression
  • Amnesia
  • Dulled Perception

Routes of Administration

No route information available yet.

Harm Reduction

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Sources

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Links

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Bretazenil - دليل المواد DrugsPRO

Bretazenil: Bretazenil (Ro16-6028) is an imidazopyrrolobenzodiazepine anxiolytic drug which is derived from the benzodiazepine family, and was invented in 1988. It is most closely related in structure to the GABA antagonist flumazenil, although its effects are somewhat different. It is classified as

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