Cagrilintide (CARGRILINTIDE) is a synthetic, long-acting amylin analogue engineered for metabolic and appetite regulation research. It is derived from the human amylin (islet amyloid polypeptide, IAPP) sequence and optimized with amino acid substitutions and a C-terminal lipid modification that significantly extend its half-life and biological stability.
In pre-clinical and in-vitro research, Cagrilintide acts as a potent dual amylin and calcitonin receptor agonist (DACRA). This dual mechanism allows it to influence satiety signaling, energy expenditure, and body weight regulation independent of insulin or glucose transport mechanisms.
Due to its long-acting pharmacological profile and receptor selectivity, Cagrilintide is frequently studied in models of obesity, metabolic syndrome, energy balance, and peptide synergy research, especially when paired with GLP-1 receptor agonists such as semaglutide or tirzepatide.
$59.00
1. Appetite Regulation and Satiety Signaling Research
2. Energy Balance and Weight Regulation Studies
3. Lipid and Glucose Metabolism Research
4. Dual Amylin–Calcitonin Receptor Mechanism Studies
5. Combination Peptide Research (Synergistic Models)
6. Pharmacokinetic and Peptide Stability Studies
This product is supplied strictly for laboratory research use only. It is not a drug, food, or cosmetic and must not be administered to humans or animals. Proper handling procedures and safety protocols should be followed by trained professionals when working with this material.
Disclaimer: For Research Use Only
All products and information presented on this website are intended solely for laboratory and scientific research purposes. Nothing contained herein should be interpreted as a recommendation, endorsement, or authorization for human consumption, medical use, or diagnostic application.
Any references to specific peptides, studies, or potential biological functions are provided strictly for informational and educational purposes. Such content must not be considered medical, health, or legal advice, nor encouragement for non-research use.
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