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cagrilintide | 10 vials
Weight Loss & Blood Sugar Regulation

Cagrilintide | 10 vials

Research Grade 10 vials
Price range: 202,99 € through 379,99 €

Cagrilintide is a long-acting synthetic analogue of the naturally occurring pancreatic hormone amylin, currently in clinical development by Novo Nordisk for chronic weight management . It represents a next-generation amylin analogue designed to overcome the short half-life limitations of earlier compounds like pramlintide .

Key Specifications:

  • CAS Number: 1415456-99-3

  • Molecular Formula: C₁₈₇H₂₉₁N₄₅O₅₉ (approx.)

  • Molecular Weight: ~4,114 g/mol

  • Purity: ≥95-98% (research grade)

  • Appearance: Lyophilized powder

  • Storage: Store at -20°C

Mechanism of Action: Cagrilintide functions as a dual amylin and calcitonin receptor agonist (DACRA) :

  • Amylin receptor (AMYR) activation: Mimics the satiety-inducing effects of natural amylin, which is co-secreted with insulin from pancreatic beta-cells

  • Calcitonin receptor (CTR) activation: Contributes to metabolic regulation through complementary pathways

  • Central nervous system action: Targets homeostatic and hedonic brain regions to reduce food intake

  • Gastric emptying: Slows gastric emptying, contributing to reduced caloric intake

Key Research Applications:

Category Applications
Obesity/Weight Management Chronic weight loss, appetite suppression
Type 2 Diabetes Adjunctive therapy for glycemic control
Metabolic disorders Combination therapy with GLP-1 agonists (CagriSema)
Diabetic kidney disease Emerging research on renal protection

Clinical Trial Data: In the Phase 3 REDEFINE 1 trial (N=3,417), cagrilintide 2.4 mg monotherapy demonstrated:

  • 11.8% mean body weight reduction after 68 weeks (vs. 2.3% placebo)

  • 31.6% of participants achieved ≥15% weight loss (vs. 4.7% placebo)

  • Average weight loss of 12.5 kg compared to 2.5 kg with placebo

  • Well-tolerated with mostly mild-to-moderate gastrointestinal effects

Important Notice: FOR RESEARCH USE ONLY. NOT FOR HUMAN USE, THERAPEUTIC, OR DIAGNOSTIC APPLICATIONS.

Cagrilintide is NOT FDA approved for any medical use (currently investigational). This product is intended for laboratory research purposes only.


Category Classification

Primary Compound Class

Cagrilintide belongs to the amylin analogue class, specifically classified as a long-acting amylin receptor agonist .

It is also classified more broadly as:

  • Dual amylin and calcitonin receptor agonist (DACRA)

  • Incretin mimetic (functionally related class)

  • Anti-obesity peptide

Mechanism-Based Classification

Classification Description
Target receptors Amylin receptors (AMY₁, AMY₃) and calcitonin receptor (CTR)
Receptor family Class B G protein-coupled receptors (GPCRs)
Primary function Reduces food intake via central satiety signaling
Cellular effects Activates Gs signaling pathways; increases cAMP in target tissues
Structural features Lipidated (acylated) for extended half-life; 95% sequence homology to tool compound 0839

Therapeutic Research Categories

Research Area Key Findings/Applications
Obesity/Weight Loss Phase 3 data shows 11.8% weight loss; dedicated RENEW program ongoing
Type 2 Diabetes Investigated in patients with obesity and T2D (RENEW 2 trial)
Combination therapy CagriSema (cagrilintide + semaglutide) shows additive/synergistic effects
Diabetic kidney disease Preliminary research suggests diabetes-specific renal effects via cAMP signaling in cortical tubules
Appetite regulation Targets homeostatic and hedonic brain regions (DVC, LPBN) via AMY₁/AMY₃ receptors

Key Points

  • Cagrilintide is a next-generation amylin analogue designed to overcome pramlintide's short half-life

  • It works through a distinct mechanism from GLP-1 agonists, offering a complementary approach to weight management

  • The peptide exhibits non-selective activation of amylin and calcitonin receptors with a unique "bypass" binding mode

  • Structural features include an E14-R17 intramolecular salt bridge enhancing helical stability, and a C-terminal P37 interaction with receptor extracellular domains

  • It is being developed both as monotherapy (RENEW program) and in combination with semaglutide (CagriSema)

Regulatory Status

Authority Status
FDA NOT approved for any medical use (investigational)
Clinical development Phase 3 trials completed (REDEFINE 1); RENEW program initiated Q4 2025
Research use Available for laboratory/preclinical research only

Important Notice: FOR RESEARCH USE ONLY. NOT FOR HUMAN USE, THERAPEUTIC, OR DIAGNOSTIC APPLICATIONS

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Key Benefits

  • High purity research compound (>98%)
  • Third-party tested and verified
  • Lyophilized for maximum stability
  • Certificate of analysis available

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