Tesofensine

Fat LossTriple monoamine reuptake inhibitor / investigationalEmerging

Tesofensine is a triple monoamine reuptake inhibitor. Tesofensine inhibits presynaptic reuptake of noradrenaline, dopamine and serotonin, raising synaptic concentrations of all three. Appetite suppression in clinical studies is attributed mainly to noradrenergic and dopaminergic signalling in hypothalamic circuits regulating food intake.

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For research use only.

Key Facts

CAS
195875-84-4
Molecular Weight (MW)
328.3 g/mol
Half-life
โ€”
FDA status
Investigational New Drug (IND)
Administration Route
oral
Frequency
โ€”
Last updated
Aug 30, 2026
Reviewed
Aug 30, 2026

Vendor price snapshot

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Vendors listing this peptide
6
Listed offers
6
Price per mg range
$179.98โ€“$1000.00/mg

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Research summary

Small-molecule triple monoamine reuptake inhibitor originally developed for neurodegenerative disease and later investigated for obesity. Not FDA-approved. It is widely sold as a research chemical despite having no approved indication in the United States.

Peptide Library's Tesofensine profile summarises 5 cited studies listed in the Science section, the compound's regulatory status, and research-protocol parameters reported for it. It is a research reference, not medical advice.

Protocol

Dosage Range
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Frequency
โ€”
Cycle
โ€”
Administration Route
oral
Reconstitution Guide
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Sequence & molecular data

Sequence and molecular data for Tesofensine
Molecular formulaC17H23Cl2NO
Molecular weight328.3 g/mol
CAS number195875-84-4
PubChem CID11370864
FDA UNIIBLH9UKX9V1
ChEMBLCHEMBL3989690
DrugBankDB06156

Identifiers link to the public PubChem, FDA Substance Registration (UNII), ChEMBL and DrugBank records for the same entity.

Science

Mechanism of Action

Tesofensine inhibits presynaptic reuptake of noradrenaline, dopamine and serotonin, raising synaptic concentrations of all three. Appetite suppression in clinical studies is attributed mainly to noradrenergic and dopaminergic signalling in hypothalamic circuits regulating food intake. Its monoaminergic activity also underlies the cardiovascular effects โ€” increases in heart rate and blood pressure โ€” reported in trials.

Regulatory & research status

Tesofensine has been studied under an Investigational New Drug application. It is not approved for marketing.

Regulatory and research status for Tesofensine
FDA statusInvestigational New Drug (IND)
Research statusInvestigational; clinical development reported
AvailabilityResearch-Only
WADA (sport)Unknown / Not Listed
Library classificationClinical Trial

Benefits

โ€”

Potential Side Effects

No side effects listed yet for this entry.

Storage & stability

Lyophilized (freeze-dried) peptide powder is far more stable than the reconstituted solution. Keep sealed vials cold, dry and away from light; long-term storage is typically frozen, with short-term refrigeration for vials in use.

Once reconstituted in bacteriostatic water, keep the solution refrigerated, avoid repeated freezeโ€“thaw cycles and agitation, and label the vial with the reconstitution date and concentration. Discard any solution that turns cloudy or shows particulates.

Degradation rates differ by sequence: peptides containing methionine, cysteine, asparagine or glutamine are more prone to oxidation and deamidation, so shelf life after reconstitution is compound-specific rather than universal.

Read the full guide: how to store peptides before and after reconstitution โ†’

Source: Manning MC, Chou DK, Murphy BM, Payne RW, Katayama DS. Stability of protein pharmaceuticals: an update. Pharm Res. 2010;27(4):544โ€“575. (PMID 20143256). General guidance for research handling; not product-specific instructions.

Tesofensine: frequently asked questions

What is Tesofensine?

Small-molecule triple monoamine reuptake inhibitor originally developed for neurodegenerative disease and later investigated for obesity. Not FDA-approved. It is widely sold as a research chemical despite having no approved indication in the United States.

How does Tesofensine work?

Tesofensine inhibits presynaptic reuptake of noradrenaline, dopamine and serotonin, raising synaptic concentrations of all three. Appetite suppression in clinical studies is attributed mainly to noradrenergic and dopaminergic signalling in hypothalamic circuits regulating food intake.

Is Tesofensine FDA approved?

No. Tesofensine is investigational: it is in clinical development and has not been approved by the FDA for any indication. Investigational status means trials are ongoing or complete but regulatory review has not resulted in approval, and efficacy and safety are still being established.

What peptides are similar to Tesofensine?

Compounds most often compared with Tesofensine include 5-Amino-1MQ, SLU-PP-332, BAM15 and AICAR. They are grouped by shared mechanism or research area rather than by equivalence, and their regulatory status and evidence base differ.

References

Related research, comparisons & guides

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Compiled by Peptide Library Editorial ยท Reviewed Aug 30, 2026 ยท Updated Aug 30, 2026 ยท Version 1

This Tesofensine profile is compiled from published literature (5 cited studies linked above), public regulatory records and chemical registries. It describes what research reports; it is not medical advice, and nothing here is a dosing recommendation for humans. Peptide Library does not sell peptides. Editorial policy ยท How profiles are compiled ยท Report an error

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