Semaglutide 5mg Research Product: Complete Scientific Overview
Order semaglutide 5mg vial. Semaglutide is a long-acting GLP-1 receptor agonist originally developed for type 2 diabetes and now widely researched for its effects on weight management, metabolic health, and neuroprotection.
What Is Semaglutide?
Semaglutide is a synthetic analog of human glucagon-like peptide-1 (GLP-1) with structural modifications that extend its half-life and enhance receptor binding affinity. Order semaglutide 5mg vial
Key Product Identifiers
| Parameter | Details |
|---|---|
| Common Names | Semaglutide |
| CAS Number | 910463-68-2 |
| Molecular Formula | C₁₈₇H₂₉₁N₄₅O₅₉ |
| Molecular Weight | 4114 g/mol |
| Sequence | His-{Aib}-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-{Lys(AEEA-AEEA-γGlu-C18 diacid)}-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-Gly |
| Structure | 31-amino-acid peptide with fatty acid side chain for albumin binding |
| Purity (Research Grade) | ≥98-99% (HPLC) |
| Storage | -20°C, lyophilized powder, protected from moisture and light |
Mechanism of Action
Semaglutide acts as a selective, competitive GLP-1 receptor agonist with an EC50 of 6.2 pM, demonstrating potent receptor binding affinity. Order semaglutide 5mg vial
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Insulin Secretion: Stimulates glucose-dependent insulin release from pancreatic β-cells
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Glucagon Suppression: Inhibits glucagon secretion from pancreatic α-cells
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Gastric Emptying: Delays gastric emptying, promoting satiety
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Appetite Regulation: Reduces appetite through central GLP-1 receptor activation
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Mitochondrial Function: Regulates mitochondrial function and lipid metabolism
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Cellular Protection: Enhances autophagy and suppresses oxidative stress and apoptosis
The Aib (2-aminoisobutyric acid) residue at position 2 and the fatty acid side chain (C18 diacid conjugated via γGlu-AEEA-AEEA linkers) enable resistance to DPP-4 degradation and reversible albumin binding, extending the peptide’s half-life.
Product Specifications: 5mg Format
Standard Product Content
Research-grade semaglutide is typically supplied as a lyophilized (freeze-dried) powder in vials containing 5mg of the peptide.
| Specification | Standard Requirement |
|---|---|
| Form | White to off-white lyophilized powder |
| Purity | ≥98% (HPLC) |
| Vial Content | 5mg peptide per vial |
| Storage | -20°C, sealed, desiccated, protected from light |
| Shelf Life | 3 years when properly stored at -20°C |
| Grade | Research use only; not for human consumption |
Reconstitution Information
Semaglutide is insoluble in water under standard conditions, but can be dissolved in:
| Solvent | Solubility | Notes |
|---|---|---|
| 0.1M NaOH | 41 mg/mL (10 mM) | Requires pH adjustment; sonication recommended |
| 0.01M HCl | 41 mg/mL (10 mM) | pH adjustment to acidic range |
| DMSO | 50 mg/mL (12 mM) | Slightly soluble; sonication recommended |
| Water (neutral pH) | Insoluble | Requires pH adjustment to ≤1 or ≥14 |
Reconstitution Method:
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Allow the vial to reach room temperature
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Add calculated volume of appropriate solvent (e.g., 0.1M NaOH) to achieve desired concentration
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Sonicate gently until completely dissolved
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Aliquot and store at -80°C for long-term stability
How Many Doses in a 5mg Vial?
A 5mg vial contains enough peptide for multiple research doses, depending on the experimental design. For reference, clinical dosing schedules are as follows:
FDA-Approved Dosing Schedules
| Brand Name | Indication | Starting Dose | Maintenance Dose | Schedule |
|---|---|---|---|---|
| Ozempic | Type 2 Diabetes | 0.25 mg weekly (4 weeks) | 0.5 mg or 1 mg weekly | Once weekly |
| Wegovy | Weight Management | 0.25 mg weekly (4 weeks) | 1.7 mg or 2.4 mg weekly | Once weekly |
| Rybelsus | Type 2 Diabetes | 3 mg daily (30 days) | 7 mg or 14 mg daily | Once daily |
Vial Yield Examples
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0.25 mg/week dose: 20 weekly injections from one 5mg vial
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0.5 mg/week dose: 10 weekly injections
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1 mg/week dose: 5 weekly injections
Research Applications
Semaglutide has been investigated across a broad range of preclinical and clinical research areas:
Metabolic Research
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Type 2 Diabetes: Potent hypoglycemic effects through GLP-1 receptor activation
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Obesity: Dose-dependent weight reduction; in DIO mouse models, 100 nmol/kg resulted in 22% body weight decrease from 43.6g to 34.8g
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Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD): Regulation of lipid metabolism
Cardiovascular Research
In doxorubicin-induced cardiac toxicity models, semaglutide (12 μg/kg/day, 6 weeks) demonstrated:
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Significant improvement in cardiac function
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Reduced myocardial injury markers
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Increased survival rates
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Inhibition of oxidative stress and mitochondrial dysfunction
Neurodegenerative Disease Research
Semaglutide has shown neuroprotective effects in:
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Parkinson’s Disease: In 6-OHDA-induced rat models, 25 nmol/kg semaglutide significantly improved neurological damage
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Potential mechanisms: Suppression of oxidative stress, enhanced autophagy, regulation of mitochondrial function
Cancer Research
GLP-1 receptor pathways are being investigated for their role in cancer metabolism and cell proliferation.
Storage and Stability
Lyophilized Powder
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Temperature: -20°C ± 5°C
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Conditions: Sealed, desiccated, protected from light
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Stability: Up to 3 years when properly stored
Reconstituted Solution
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Short-term: -80°C for up to 1 year
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Avoid freeze-thaw cycles to prevent peptide degradation
Quality Considerations
Research-Grade Quality Standards
Premium semaglutide research products should include:
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HPLC purity analysis (≥98-99%)
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Mass spectrometry verification of molecular weight (~4114 Da)
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Third-party laboratory testing documentation
Manufacturing Standards
Products manufactured under:
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GMP (Good Manufacturing Practice) guidelines
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ISO 9001 certification
Research Dosage Guidance
Preclinical studies have utilized semaglutide across a range of dosages:
| Research Model | Dosage | Route | Citation |
|---|---|---|---|
| DIO Mouse (obesity) | 1, 3, 10, 30, 100 nmol/kg | Subcutaneous | |
| Cardiac Toxicity (mouse) | 12 μg/kg/day (6 weeks) | Subcutaneous | |
| Parkinson’s Disease (rat) | 25 nmol/kg (every 2 days, 31 days) | Intraperitoneal | |
| In vitro cell studies | 1-100 nM | Cell culture |
Switching from Other GLP-1 Agonists
For researchers modeling transitions between GLP-1 therapies, a conservative approach is recommended when switching from liraglutide (Saxenda®) to semaglutide:
| Current Liraglutide Dose | Suggested Semaglutide, Starting Dose |
|---|---|
| 0.6 mg/day | 0.25 mg/week |
| 1.2 mg/day | 0.25 mg/week |
| 1.8 mg/day | 0.25 or 0.5 mg/week |
| 2.4 mg/day | 0.25 or 0.5 mg/week |
| 3.0 mg/day | 0.5 mg/week |
No washout period is required; semaglutide can be started the day after stopping liraglutide.
Summary of Key Research Applications
| Application Area | Key Findings | Citation |
|---|---|---|
| Type 2 Diabetes | Potent glycemic control via GLP-1R activation | |
| Obesity | Dose-dependent weight reduction; 22% loss in mouse models | |
| Cardiovascular | Improved function; reduced injury markers; increased survival | |
| Neurodegenerative | Neuroprotection in Parkinson’s models | |
| Liver/Metabolic | Regulation of lipid metabolism in MASLD | |
| Mitochondrial Function | Repairs dysfunction; reduces oxidative stress |




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