Library

Memantinas

Memantine is an adamantane derivative and NMDA receptor antagonist primarily prescribed for the management of moderate-to-severe Alzheimer's disease. It works by blocking glutamate-mediated neuronal excitotoxicity, distinguishing it mechanistically from the cholinesterase inhibitors typically used in Alzheimer's treatment. At supratherapeutic doses, memantine can produce prolonged dissociative effects reportedly lasting 16 or more hours, placing it among the longest-duration dissociatives available.

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

Also known as: Dmaa, Ebixa, Axura, D-145, Memaxa, Namenda, Akatinol, Memantinum, Memantina, DRG-0267, Dimethylamylamine, 1,3-DMAA, Methylhexanamine

Classification

  • Chemical: Medicine
  • Psychoactive: Dissociative
  • Psychoactive: Nootropic
  • Psychoactive: Stimulant
  • Tag: adamantane
  • Tag: Adamantane derivative
  • Tag: Habit-Forming
  • Tag: Pharmaceutical
  • Tag: Research-Chemical
  • Tag: Tentative

Effects

  • Sedation
  • Stimulation
  • Incoordination
  • Nausea
  • Insomnia
  • Bodily Buzzing
  • Confusion
  • Anxiety
  • Dissociation
  • Memory Suppression
  • Dizziness
  • Motor Control Loss
  • Hallucinations
  • Open Eye Visuals
  • Visual Trails
  • Closed Eye Visuals
  • Double Vision
  • Increased Libido

Routes of Administration

Oral

Dosage

  • Heavy: 40-80 mg
  • Light: 10 – 30 mg
  • Common: 30 – 50 mg
  • Strong: 50 – 80 mg
  • Threshold: 5-10 mg

Duration

  • Onset: 0.5-1.5 h
  • Comeup: 2-3 h
  • Peak: 3-12 h
  • Offset: 5-24 h
  • After Effects: 24-72 h
  • Total Duration: 8-24 h

Harm Reduction

Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.

Sources

Substance data is aggregated from the following public harm-reduction and reference sources.

Links

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Memantine - DrugsPRO substancijos vadovas

Memantine: Memantine is an adamantane derivative and NMDA receptor antagonist primarily prescribed for the management of moderate-to-severe Alzheimer's disease. It works by blocking glutamate-mediated neuronal excitotoxicity, distinguishing it mechanistically from the cholinesterase inhibitors typic

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