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All products discussed on this site are Research Use Only (RUO) compounds intended strictly for laboratory research. Nothing here is medical advice, and these products are not for human or veterinary use.

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Tesofensine: Research Profile, Dosages & Supplier Prices

Metabolic research (small molecule) · Powder (oral small molecule) · Also known as: NS2330, triple monoamine reuptake inhibitor

Tesofensine is a metabolic research (small molecule) compound with a molecular weight of 328.3 g/mol and a research half-life of ~8-9 days (very long). Tesofensine is a triple monoamine reuptake inhibitor - blocking serotonin, norepinephrine and dopamine reuptake - originally developed for Parkinson's and Alzheimer's disease. During those trials researchers noticed substantial, dose-dependent weight loss, and development pivoted to obesity, where Phase 2 data showed weight loss roughly double that of then-available medications.

Research Use Only (RUO). Not for human or veterinary use. Not medical advice.

SequenceNon-peptide small molecule
FormulaC17H23Cl2NO
Mol. weight328.3 g/mol
Half-life~8-9 days (very long)
Forms soldPowder (oral small molecule)

What is Tesofensine?

Its weight-loss effect comes from combined appetite suppression and increased energy expenditure and fat oxidation, driven by the triple neurotransmitter action. Though not a peptide, it is a staple of metabolic research catalogs and is frequently studied alongside GLP-1 agonists as a mechanistically distinct (central monoaminergic vs incretin) approach. The very long half-life of over a week is a defining pharmacokinetic feature.

Mechanism of Action (Research Context)

Triple reuptake inhibitor of serotonin, norepinephrine and dopamine transporters (SERT/NET/DAT). Central appetite suppression plus increased thermogenesis and fat oxidation; dopaminergic action modulates food reward pathways.

Research Areas

Obesity and appetite regulationMonoamine transporter pharmacologyEnergy expenditure / thermogenesisFood reward signaling

Tesofensine Dosages in Research

0.25mg0.5mg1mg (trial reference doses)

Phase 2 obesity trials used 0.25-1 mg once daily. Microgram-to-milligram compound with ~8-9 day half-life. Research-context only.

Dosage information is a summary of published laboratory research and is provided for informational purposes only. These compounds are not for human use.

Storage & Handling

Powder: room temperature desiccated or 2-8C, protected from light. Stable small molecule.

Tesofensine Supplier Price Comparison

No tracked suppliers stock Tesofensine yet — inventory syncs run continuously. Check our supplier reviews.

Tesofensine FAQ

No - it is a small-molecule triple monoamine reuptake inhibitor. It appears in metabolic research catalogs because it is studied for the same obesity research questions as GLP-1 peptides.
Obesity primarily: Phase 2 trials showed roughly double the weight loss of older medications. Mechanistically it combines appetite suppression with increased energy expenditure via serotonin, norepinephrine and dopamine reuptake blockade.
98%+ HPLC purity and mass spec identity at 328.3 Da. Note the long half-life means steady-state accumulation matters in study design.
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