Tesofensine is a triple-monoamine reuptake inhibitor originally developed for neurodegenerative disorders but repurposed for obesity treatment. Clinical pharmacokinetics show an elimination half-life of ≈220 hours with an active N-desalkyl metabolite (NS2360) lasting ≈374 hours; steady-state is reached only after 4-5 weeks. Single overdoses can linger for over a week. Community reports emphasize starting at ≤0.25 mg every 48 hours to limit insomnia, anxiety, and heart rate increases (8-15 bpm above baseline). Research chemical vendor authenticity varies; reagent testing with TLC plus chiral GC-MS is advised.
טסופנסין molecular structure diagram from the DrugsPRO substance library.
Also known as: Te, Ns-2330
Classification
Chemical: Tropane
Psychoactive: Stimulant
Tag: Appetite-suppressant
Tag: Phenyltropane
Tag: Research-Chemical
Effects
Mental Stimulation
Dry Mouth
Insomnia
Tachycardia
Diarrhea
Nausea
Motivation Enhancement
Focus Enhancement
Anxiety
Talkativeness
Alertness Enhancement
Thought Acceleration
Appetite Suppression
Light Sensitivity
Increased Libido
Disinhibition
Dehydration
Tactile Enhancement
Routes of Administration
Oral
Dosage
Threshold: 0.05 mg
Light: 0.05-0.20 mg
Common: 0.20-0.50 mg
Strong: 0.50-1 mg
Heavy: 1 mg
Duration
Onset: 0.5-2 h
Comeup: 2-4 h
Peak: 4-10 h
Offset: 12-24 h
After Effects: 24-72 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.
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Tesofensine - מדריך חומרים של DrugsPRO
Tesofensine: Tesofensine is a triple-monoamine reuptake inhibitor originally developed for neurodegenerative disorders but repurposed for obesity treatment. Clinical pharmacokinetics show an elimination half-life of ≈220 hours with an active N-desalkyl metabolite (NS2360) lasting ≈374 hours; steady-