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Tesamorelin 10mg 10vials

Tesamorelin 10mg 10vials

Original price was: $600.00.Current price is: $300.00.

Tesamorelin is a synthetic 44-amino acid GHRH analog featuring an N-terminal trans-3-hexenoic acid modification for enhanced DPP-4 resistance and a 40-50 minute half-life. It stimulates reliable pulsatile GH release specifically targeting visceral adipose tissue lipolysis.

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Description

Tesamorelin Long-Acting GHRH Analog Research Peptide

Pharmacodynamics

Tesamorelin actively targets and binds to the GHRH receptors of the anterior pituitary. This highly specific binding interaction initiates a cyclic AMP-dependent intracellular signaling cascade. The cascade subsequently forces intense pulsatile exocytosis of growth hormone vesicles. Compared to shorter, unmodified analogs like Sermorelin, the lipid group modification at the N-terminus dramatically enhances the peptide’s resistance to dipeptidyl peptidase-4 (DPP-4) enzymatic cleavage. Quantitative pharmacokinetic data confirms this trait extends the biological half-life in vivo to approximately 40 to 50 minutes. This extended receptor activation provides a more robust, sustained GH pulse, which has been shown in clinical research models to heavily upregulate targeted adipocyte lipolysis.

About This Compound

Tesamorelin is a synthetic 44-amino acid polypeptide structurally equivalent to endogenous growth hormone-releasing hormone. By strategically integrating a trans-3-hexenoic acid group at the N-terminus, researchers have developed a highly stable compound specifically for evaluating lipid metabolism and basal GH restoration targeting visceral adipose tissue.

Specification Sheet

  • Sequence Modification: N-terminal trans-3-hexenoic acid linked to 44-amino acid chain
  • Molecular Formula: C211H366N72O67S
  • Molecular Weight: 5135.9 g/mol
  • Purity: >99% (HPLC validated)
  • Appearance: Sterile filtered white lyophilized powder

Known Effects

  • Research models indicate noticeable, targeted reductions in trunk and visceral adipose deposits.
  • Study data demonstrates improved overall lipid profiles, such as triglycerides, during sustained research protocols.
  • Multiple research groups note enhanced deep slow-wave sleep architecture and accelerated musculoskeletal recovery.
  • Researchers observe a continuous, stable elevation in circulating IGF-1 without disrupting natural endocrine feedback loops.

In Brief:
Tesamorelin offers researchers a highly stable, long-acting GHRH analog with unparalleled targeting potential for evaluating visceral lipolysis and endogenous GH pulsing.

Frequently Asked Questions

[Q] How does Tesamorelin differ from CJC-1295?

Tesamorelin contains the full 44-amino acid sequence with a specific lipid modification, showing a stronger clinical track record for targeted visceral fat lipolysis.

[Q] Must it be administered in a fasted state?

Yes, any elevation in systemic insulin from food intake will immediately block the peptide’s ability to stimulate pituitary growth hormone release.

[Q] Why do I experience a facial flush after injecting?

This is a completely normal, harmless physiological reaction caused by the rapid localized vasodilation when the compound enters systemic circulation.

[Q] How long does a reconstituted vial of Tesamorelin last?

When properly reconstituted with Bacteriostatic Bac.water and continuously refrigerated at 2??C to 8??C, the peptide solution remains active for approximately 14 to 21 days.

[Q] Can it be combined with other secretagogues?

Yes, advanced researchers frequently stack GHRH analogs like Tesamorelin with a ghrelin agonist like Ipamorelin to evaluate massive synergistic pulse effects.

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. Consult a qualified healthcare professional before use.

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