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Research-grade compound. Laboratory use only. Not intended for human or animal use, ingestion, or injection. No medical claims are made or implied.

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Research-grade Tesofensine. 99.3% avg purity, HPLC & MS verified. Oral tablets in sealed bottle. For laboratory research use only. Not for human consumption.
| Quantity | Price Each | Total | Savings |
|---|---|---|---|
| 1 unit | €150.99 | €150.99 | -- |
| 3+ | €143.44 | €430.32 | 5% off |
| 5+Most Popular | €135.89 | €679.46 | 10% off |
| 10+ | €128.34 | €1,283.42 | 15% off |
Free shipping on orders over €200
Important Notice
This product is intended for laboratory and research use only. Not for human or veterinary use. By purchasing, you confirm this product will be used exclusively for in-vitro research purposes.
99.3% average HPLC purity, verified by independent third-party testing
Janoshik report published when available
24h dispatch, EU-wide shipping from €4.99
Independent lab verification for every batch
This compound was developed for Parkinson disease. The metabolic endpoint research was an accident. NeuroSearch ran Phase 2 trials in Parkinson and Alzheimer subjects, observed unremarkable neurological effects, and noticed unexpected substantial metabolic endpoint changes as a secondary finding. That result reoriented the development program. CAS: 402856-42-2. MW 395.9 Da. Tesofensine is a triple monoamine reuptake inhibitor — blocking serotonin, dopamine, and norepinephrine transporters simultaneously.
This is not incretin pharmacology. GLP-1 agonists work through hormonal receptor signaling. Tesofensine works through monoamine reuptake inhibition: serotonin drives satiety via hypothalamic 5-HT receptors, norepinephrine increases sympathetic tone and thermogenesis, dopamine modulates reward circuits and food-seeking behavior. Three systems, all at once, through neural rather than endocrine pathways.
The pharmacological overlap with sibutramine (the withdrawn dual SNRI) is real but shouldn't be overstated. Sibutramine's cardiovascular liability was specifically about sympathomimetic cardiovascular effects. Tesofensine has a distinct receptor affinity profile and different pharmacokinetics — worth distinguishing carefully in research design. Phase 2b TIPO-1 trial data showed dose-dependent metabolic endpoint changes that caught the field's attention and drove the subsequent development interest in central mechanisms as an alternative to incretin pathways.
| Molecular Weight | 395.9 Da |
|---|---|
| CAS | 402856-42-2 |
| Purity | 99.3% avg by HPLC |
| Form | Capsule |
| Sizes | 500mcg (60 capsules) |
Storage: Room temperature, away from moisture and direct light.
Quality: HPLC purity analysis, mass spec identity confirmation, endotoxin testing on every batch. COA ships with every order. EU-based QC under CERTALAB S.R.L.
GLP-1 agonists work through hormonal receptor pathways — they mimic an incretin hormone and signal through the GLP-1 receptor to affect insulin, appetite, and gastric emptying. Tesofensine works centrally, blocking reuptake of three monoamines (serotonin, dopamine, norepinephrine) to modulate appetite circuits and metabolic rate through neural pathways. The two mechanisms are independent, which is why they're sometimes studied in combination for additive effects.
There's a pharmacological overlap — both inhibit monoamine reuptake — but the profiles differ. Sibutramine was a dual SNRI (serotonin and norepinephrine). Tesofensine adds dopamine reuptake inhibition and has a different receptor affinity profile overall. Sibutramine was withdrawn for cardiovascular reasons tied to sympathomimetic effects; tesofensine's cardiovascular profile in research contexts is different and should be evaluated on its own data rather than by analogy.
For research purposes only. Not for human consumption.
Researcher Confidence
Who actually tests this?
Every batch is independently verified by Janoshik Analytical (100,000+ verifications/month), Eurofins Scientific, and Analytical Sciences International. We publish every Certificate of Analysis.
View COAs →What if I get the wrong batch?
Every bottle label carries a lot number that maps to a specific Certificate of Analysis. If a batch fails spec, we don't ship it — full stop.
View COAs →Where does it ship from?
Romania (EU). We are CERTALAB SRL, CUI RO54451735, VAT-registered. SameDay for Romania, FanCourier for Central/Eastern EU, TCE Worldwide for the rest. 3–7 business days EU-wide.
Shipping details →What if there's a problem?
You have a 14-day withdrawal right under OUG 34/2014 (Romanian/EU consumer law), with ANPC/ODR escalation available. Contact us at support@certapeptides.com.
Returns policy →This product is intended for scientific research and development purposes only. It is a chemical substance that shall not be used as a drug, medicine, active substance, or ingredient in any product intended for human or animal consumption. Researchers must handle this compound in accordance with their institutional biosafety guidelines. Use only in properly equipped laboratory settings with appropriate personal protective equipment.
500mcgSAME FIELDKPV is a naturally occurring tripeptide (Lys-Pro-Val) derived from the C-terminal end of alpha-melanocyte-stimulating hormone (alpha-MSH). It has been studied for its immunomodulatory signaling in gastrointestinal and immune biology research models. Alpha-MSH-derived immunomodulatory tripeptide Intestinal epithelial barrier and PepT1 transporter research NF-kB pathway modulation studies For research purposes only. Not for human consumption.
SAME FIELDOral Semaglutide capsules for research into GLP-1 receptor agonism via enteric delivery. Available in 3mg and 7mg formulations. Supplied at 99.3% avg purity (HPLC-verified), with a Certificate of Analysis for every batch. Key research areas: Oral peptide bioavailability and absorption kinetics GLP-1 receptor-mediated glucose homeostasis Enteric coating and SNAC co-formulation studies For research purposes only. Not for human consumption.
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