Orforglipron CAS 2212020-52-3

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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