Library

Ciklazodon

Cyclazodone is a centrally acting stimulant developed in the 1960s, structurally related to pemoline and 4-methylaminorex. It appeared on the research chemical market in 2017 with limited pharmacological data. While animal studies suggest lower cardiotoxicity and hepatotoxicity than amphetamine, the structurally related pemoline was withdrawn due to causing liver damage in children. Heavy or sustained usage may result in liver damage. Use accurate scales, start with low doses, and employ harm reduction practices.

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

Also known as: Cyclazadone, Cyclopropylpemoline, N-cyclopropylpemoline, NCP-pemoline

Classification

  • Chemical: Aminorex
  • Psychoactive: Nootropic
  • Psychoactive: Stimulant
  • Tag: 4-oxazolidinone
  • Tag: Oxazolinone
  • Tag: Research-Chemical
  • Tag: Aminorex

Effects

  • Stimulation
  • Physical Euphoria
  • Stamina Enhancement
  • Loss Of Appetite
  • Physical Energy
  • Teeth Grinding
  • Focus Enhancement
  • Motivation Enhancement
  • Wakefulness
  • Cognitive Euphoria
  • Analysis Enhancement
  • Thought Acceleration
  • Bodily Control Enhancement
  • Appetite Suppression
  • Increased Libido
  • Light Sensitivity
  • Increased Music Appreciation
  • Dehydration

Routes of Administration

Oral

Dosage

  • Threshold: 2–5 mg
  • Light: 5-10 mg
  • Common: 10-20 mg
  • Strong: 20-30 mg
  • Heavy: 35 mg+

Duration

  • Onset: 0.3-0.8 h
  • Comeup: 0.5-1 h
  • Peak: 2-4 h
  • Offset: 1-2 h
  • After Effects: 1-12 h
  • Total Duration: 5-8 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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Cyclazodone - DrugsPRO anyag útmutató

Cyclazodone: Cyclazodone is a centrally acting stimulant developed in the 1960s, structurally related to pemoline and 4-methylaminorex. It appeared on the research chemical market in 2017 with limited pharmacological data. While animal studies suggest lower cardiotoxicity and hepatotoxicity than amp

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