
Orforglipron CAS 2212020-52-3
Orforglipron (CAS 2212020-52-3) is a first-in-class, small-molecule, oral GLP-1 receptor agonist currently under clinical research for obesity management, weight loss, and type 2 diabetes.
- Product Introduction
Orforglipron (CAS 2212020-52-3) – Next-Generation Oral GLP-1 Receptor Agonist
What is Orforglipron?
Orforglipron (CAS 2212020-52-3) is a first-in-class, small-molecule, oral GLP-1 receptor agonist currently under clinical research for obesity management, weight loss, and type 2 diabetes.
Unlike traditional peptide-based GLP-1 analogs such as Semaglutide or Tirzepatide, Orforglipron is non-peptidic-making it more stable, easier to formulate, and suitable for oral delivery without injection.
This innovation represents a major advancement in metabolic and obesity research, enabling scientists to explore new pathways of appetite regulation, energy expenditure, and glucose homeostasis.
Key Benefits & Research Applications
For research and development use, Orforglipron has demonstrated potential in:
- Weight-Loss Studies – Promotes satiety and reduces caloric intake via GLP-1 pathway activation.
- Metabolic Regulation – Improves glucose tolerance and insulin sensitivity in preclinical models.
- Energy Balance Research – Enhances energy expenditure and lipid metabolism.
- Appetite Control Mechanisms – Modulates hypothalamic signaling related to hunger and satiety.
- Oral Formulation Studies – Ideal model compound for evaluating oral GLP-1 analog bioavailability and stability.
Molecular Structure & Chemical Information
- Chemical Name: Orforglipron
- CAS Number: 2212020-52-3
- Molecular Formula: C₂₁H₂₃N₅O₃
- Molecular Weight: ~393.44 g/mol
- Purity: ≥98% (HPLC verified)
- Form: White or off-white powder
- Solubility: Soluble in DMSO, ethanol, and methanol
Mechanism of Action
Orforglipron is a selective GLP-1 receptor agonist, binding to the receptor and mimicking the activity of natural GLP-1 (glucagon-like peptide-1).
- This receptor activation triggers downstream signaling that.
- Enhances insulin secretion in response to glucose
- Suppresses glucagon release
- Slows gastric emptying, leading to prolonged satiety
- Decreases appetite and caloric intake
Unlike peptide GLP-1 drugs, Orforglipron is non-degradable by digestive enzymes, allowing oral dosing and consistent receptor activation.
Comparison with Other GLP-1 Compounds
|
Compound |
Type |
Administration |
Key Benefit |
Notes |
|
Orforglipron |
Non-peptide GLP-1 agonist |
Oral |
Stable, convenient, cost-efficient |
New generation |
|
Semaglutide |
Peptide GLP-1 agonist |
Injection or oral |
Potent, clinically proven |
Requires stabilization |
|
Tirzepatide |
Dual GIP/GLP-1 peptide |
Injection |
Dual receptor activity |
Injectable only |
|
Liraglutide |
Peptide GLP-1 agonist |
Injection |
Long-acting peptide |
Less oral stability |
Orforglipron stands out as a non-peptidic oral molecule, potentially transforming obesity and diabetes research through improved delivery and metabolic durability.
Storage & Stability
Storage Temperature: –20 °C (long term)
Protect From: Light, moisture, and heat
Shelf Life: ≥3 years under proper storage
Reconstitution: Dissolve in DMSO or ethanol for research use
Note: For laboratory research only. Not approved for human or veterinary use.
Safety & Handling
Handle with standard laboratory PPE (gloves, goggles, lab coat).
Avoid inhalation, ingestion, or contact with skin.
Dispose of according to institutional biosafety guidelines.
FAQ
Q1: What makes Orforglipron unique?
A: It's the first orally active, non-peptide GLP-1 receptor agonist, eliminating the need for injections and improving formulation versatility.
Q2: How does it differ from Semaglutide or Tirzepatide?
A: Orforglipron is small-molecule, not peptide-based, giving it higher chemical stability and oral bioavailability.
Q3: Can Orforglipron be used with other metabolic agents?
A: Research studies often combine GLP-1 agonists with AMPK activators or SGLT2 inhibitors to explore synergistic metabolic effects.
Q4: Is Orforglipron available in bulk?
A: Yes - we supply bulk and small-quantity Orforglipron for R&D applications worldwide, with full COA and MSDS documentation.
Conclusion
Orforglipron (CAS 2212020-52-3) represents the future of GLP-1 agonist research - a small, stable, oral compound offering insight into fat loss, appetite control, and metabolic regulation.
For laboratories investigating non-peptide metabolic modulators, Orforglipron is an ideal choice due to its oral activity, stability, and GLP-1 receptor specificity.
Why Choose Us as Your Orforglipron Supplier?
High Purity (≥98%) verified by HPLC and MS
COA & MSDS Provided with every batch
Global Shipping with temperature-controlled packaging
Bulk & Custom Quantities available
Expert Technical Support for metabolic and GLP-1 pathway research
Competitive Pricing for universities, biotech, and R&D institutions
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Meta Description
Buy Orforglipron (CAS 2212020-52-3) – a next-generation oral GLP-1 receptor agonist for metabolic and obesity research. High-purity non-peptide compound for advanced weight-management studies.

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