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Semaglutide 5mg

$ 224,400

  • GLP-1 receptor agonist for advanced metabolic research.
  • Supports appetite control and glycemic regulation.
  • Contributes to the study of insulin sensitivity and energy metabolism.
  • High-purity compound, designed exclusively for research purposes.

 

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Description
🔹 IN-DEPTH SCIENTIFIC PROFILE

Semaglutide is a synthetic analog of glucagon-like peptide-1 (GLP-1) with 94% homology to native human GLP-1. This 31-amino-acid peptide (MW: 4113.58 Da) incorporates strategic modifications that extend its half-life:

Structural Modifications:

Substitution of Alanine by 2-aminoisobutyric acid (AIB) at position 8
Acylation at Lysine-26 with a C18 fatty acid via a spacer
A hydrophobic side chain that facilitates binding to serum albumin (>99%)

Molecular Mechanisms:

  • GLP-1R receptor: Selective activation in pancreatic β-cells, hypothalamus, and gastrointestinal tract
    cAMP/PKA pathway: Increase in intracellular cyclic AMP → glucose-dependent insulin secretion
  • Glucagon Suppression: Pancreatic alpha-cell inhibition during hyperglycemia
    Gastric Emptying: Delay Mediated by Vagal Signaling (70% Reduction)
  • Central Satiety Activation of POMC/CART neurons in the hypothalamic arcuate nucleus

Advanced Pharmacokinetics:

  • Subcutaneous bioavailability: 89%
  • Tmáx: 1-3 days post-injection
  • Median life 165-184 hours (weekly administration)
  • Renal clearance: <1% (primary proteolytic degradation)
  • Steady state: 4-5 weeks
🔹 APPLICATIONS, MECHANISMS, AND EXTENDED RESEARCH

Metabolic Regulation in Experimental Models
Glycemic Control

  • HbA1c reduction: 1.5–2.01 TP3T in diabetic models (Aroda et al., 2017)
  • Increased insulin secretion: 200-300% during oral tolerance testing
  • Improves insulin sensitivity: Reduced HOMA-IR index 40-50%

Body Weight Modulation:

  • Weight reduction: 12-15% in long-term studies (68 weeks) (Wilding et al., 2021)
  • Visceral fat loss: 25-30% above the subcutaneous tissue
  • Lean mass preservation: A loss of 85-90% corresponds to adipose tissue

Cardiovascular Effects (SUSTAIN Studies):

  • Reduction of MACE events: 26% vs. placebo (Marso et al., 2016)
  • Decrease in systolic blood pressure: 4-6 mmHg
  • Improves lipid profile: triglyceride reduction 15-20%

Neuroprotection and Cognitive Function

Neurodegeneration Models:

  • Reduction of beta-amyloid plaques in Alzheimer's models: 30-40% (Cai et al., 2018)
  • Prevention of dopaminergic neuronal loss in Parkinson's
  • Attenuation of neuroinflammation: decrease in IL-6, TNF-α (50–60%)

Synaptic Plasticity:

  • Increase in BDNF (Brain-Derived Neurotrophic Factor): 25-35%
  • Improved hippocampal long-term potentiation (LTP)
  • Neurogenesis in the dentate gyrus: increase 40%
🔹 ADVANCED RESEARCH PROTOCOLS

Dosing in Animal Models

Species Application Dosage Range Frequency Way
Mice Glycemic control 5-20 nmol/kg Weekly SC
Mice Weight reduction 10-50 nmol/kg Weekly SC
Primates Cardiovascular studies 2-10 nmol/kg Weekly SC

In Vitro Studies

Cell Cultures:

  • Pancreatic β cells (INS-1): 1-100 nM in complete medium.
  • Primary neurons: 10-50 nM with 48-72h exposure.
  • 3T3-L1 adipocytes 5-25 nM during differentiation.
🔹 OPTIMIZED RECONSTITUTION METHODS

Standard Protocol:

  1. Use sterile bacteriostatic water (pH 7.0-7.4)
  2. For 5mg vial: add 2.0mL → concentration 2.5mg/mL
  3. Inject slowly down the vial wall (avoid foaming)
  4. Gently roll for 30-60 seconds (DO NOT shake vigorously)
  5. Check for clear, particle-free solution

Post-Reconstitution Storage:

  • Refrigeration: 2-8°C for up to 56 days
  • Protect from direct light (amber vials recommended)
  • Prevent complete freezing (<-20°C)
  • Allow to reach room temperature before administration
🔹 RESEARCH FAQ

Q: How does Semaglutide compare to other GLP-1 agonists? R: It presents a higher affinity for GLP-1R (EC50: 0.38 nM vs 1-5 nM for liraglutide) and a 7-fold longer half-life, allowing for weekly administration versus daily.

P: Is it compatible for research in combination with insulin? A: Yes, studies show a synergistic effect on glycemic control with a 30% reduction in the required insulin dose (Aroda et al., 2017).

Q: What biochemical markers should be monitored in prolonged studies? R: Plasma glucose, HbA1c, C-peptide, glucagon, serum lipase, renal function (creatinine, BUN), and inflammatory markers (CRP, IL-6).

P: What is the optimal timing for metabolic evaluations? R: Steady state reached in 4-5 weeks; continuous glycemic measurements require at least 8 weeks for full effects.

🔹 RESEARCH REFERENCES
  1. Aroda VR, et al. (2017) “Efficacy and safety of once-weekly semaglutide versus once-daily insulin glargine” – Lancet Diabetes Endocrinol 5(5):355-366. [PubMed: 28344112]
  2. Wilding JPH, et al. (2021) “Once-Weekly Semaglutide in Adults with Overweight or Obesity” - The New England Journal of Medicine384(11):989-1002. [PubMed: 33567185]
  3. Marso SP, et al. (2016) “Semaglutide and Cardiovascular Outcomes in Diabetes” – The New England Journal of Medicine 375(19):1834-1844. [PubMed: 27633186]
  4. Cai HY, et al. (2018) “GLP-1 treatment protects Alzheimer model through enhancing neuronal insulin signaling” – Brain Res 1678:64-72. [PubMed: 29128461]
  5. Novo Nordisk Research (2017) “Pharmacokinetic properties of semaglutide” – Diabetes Obes Metab 19(1):140-147.
🔹 COA Certificate

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🔹 Endotoxin Certificate

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Research material only. This product is intended for scientific research in controlled laboratory settings only. It is not a drug. Not for human or animal use, not for diagnostic or therapeutic use.

Legal Notice

All products are sold in powder (lyophilized) form and require reconstitution with a suitable diluent for research purposes only. Laboratory supplies (e.g., syringes, bacteriostatic water, etc.) are not included. Dosage instructions are not provided.

We comply with all local and national laws and regulations related to product sales. exclusively for research.
We are not a pharmacy, nor do we offer, promote, or provide any advice for human or animal consumption.

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