Cagrilintide
Cagrilintide is a synthetic, long-acting analog of amylin, studied for activation of target receptor pathways and characterization of endocrine and neuroendocrine signaling.
Wholesale Pricing
Available Doses & Tiered Pricing
Cagrilintide 10mg
Save 33%- 50 vials$45.00 / vial
- 100 vials$40.00 / vial
- 250 vials$35.00 / vial
- 500 vials★ Best Value$30.00 / vial
Overview
Cagrilintide is a synthetic, long-acting analog of amylin, studied for activation of target receptor pathways and characterization of endocrine and neuroendocrine signaling.
History
Developed as a stabilized amylin analog with prolonged target activity for studying calcitonin receptor family signaling.
Key Areas of Research
- Receptor binding and cascades
- Amylin pathways and downstream markers
- Signaling homeostasis
References
- Granhall C. et al. (2019). PK/safety of cagrilintide. Clin Pharmacokinet 58(10):1391–1402.
- Enebo L.B. et al. (2021). Cagrilintide + semaglutide. Lancet 397:1736–1748.
Research Use Only
All products are intended solely for laboratory research purposes and are not for human or animal consumption. Must be handled by qualified professionals.
Related Compounds
GLP-1 & Metabolic
Semaglutide
Semaglutide is a synthetic peptide analog that functions as a long-acting pathway agonist, structurally modified for extended half-life and improved target binding affinity. It is studied in preclinical and laboratory models for its ability to activate target pathways and modulate downstream molecular signaling associated with endocrine regulation.
View details →GLP-1 & Metabolic
Tirzepatide
Tirzepatide is a synthetic peptide that functions as a dual pathway agonist, designed as a once-weekly investigational compound studied in preclinical laboratory models for receptor-mediated signaling and modulation of downstream cascades.
View details →GLP-1 & Metabolic
Retatrutide
Retatrutide is a synthetic investigational peptide developed as a multi-pathway agonist, representing the next generation of metabolic research compounds. It activates multiple target receptor subtypes for broad systemic effects studied in preclinical models.
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