Peptide Registry

Tesofensine (NS2330)

$139.00

  • Contents: Tesofensine (NS2330; triple DAT/NET/SERT reuptake inhibitor small molecule)
  • Format: Encapsulated solid
  • Appearance: White to off-white solid
  • Purity: >99%
Quantity Discount Price
1 - 3 - $139.00
4 - 7 10% $125.10
8 + 18% $113.98
SKU: N/A Category: Brand:

Description

Tesofensine (NS2330) is an orally bioavailable synthetic small molecule that simultaneously inhibits the dopamine transporter (DAT; IC50 6.5 nM), norepinephrine transporter (NET; IC50 1.7 nM), and serotonin transporter (SERT; IC50 11 nM), elevating synaptic concentrations of all three monoamines through balanced transporter inhibition. Its long plasma half-life of approximately 234 hours produces sustained steady-state monoamine transporter inhibition relevant to chronic CNS signaling research protocols. Originally investigated in clinical trials for Parkinson’s disease and multiple metabolic research programs, it provides a defined three-transporter reference compound for research where simultaneous DAT, NET, and SERT inhibition are the experimental variables.

Storage and Handling

Store in a cool, dry place away from heat, moisture, and direct light. Keep container tightly sealed when not in use. Tesofensine is stable under standard ambient storage conditions; refer to the lot-specific certificate of analysis for specific requirements.

Compliance Notice

Tesofensine capsules are for laboratory research use only. They are not for human or veterinary use and carry no therapeutic, diagnostic, or clinical indication. FDA has not evaluated this product. By purchasing this product, the buyer confirms that they will follow appropriate institutional safety procedures and use it exclusively for controlled research.

Frequently Asked Questions

What makes Tesofensine a distinct research tool compared to selective monoamine reuptake inhibitors?

Selective reuptake inhibitors isolate individual transporter pharmacology. Tesofensine simultaneously inhibits DAT, NET, and SERT at nanomolar potency, producing combined monoaminergic input that selective inhibitors cannot replicate. Researchers studying how simultaneous three-transporter inhibition affects synaptic monoamine dynamics and downstream signaling use Tesofensine as the triple-inhibitor reference compound.

Why is capsule format appropriate for Tesofensine research?

Tesofensine is an orally bioavailable small molecule with a documented plasma half-life of approximately 234 hours following oral administration. Its long half-life produces sustained steady-state transporter inhibition relevant to chronic CNS signaling protocols, making capsule format the mechanistically appropriate delivery method.