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COMPOUND OVERVIEW
Ipamorelin is a selective pentapeptide growth hormone secretagogue (GHS) and ghrelin receptor agonist that stimulates GH release from the anterior pituitary with high selectivity and minimal off-target effects. Developed as a research tool for studying the GH axis, Ipamorelin is notable for its clean pharmacological profile — it stimulates GH release without meaningfully affecting cortisol, prolactin, or ACTH levels at research-relevant doses. This selectivity has made it a preferred choice in GH research, often combined with GHRH analogues like CJC-1295 to maximize GH pulse amplitude.
MECHANISM OF ACTION
Ipamorelin acts as an agonist at the ghrelin receptor (GHS-R1a) on pituitary somatotrophs, triggering intracellular calcium mobilization and GH exocytosis. Unlike first-generation GHRPs (GHRP-2, GHRP-6), Ipamorelin does not significantly stimulate cortisol, ACTH, or prolactin secretion, making it a cleaner research molecule for studying isolated GH axis effects. Its synergy with GHRH analogues operates through complementary receptor pathways — CJC-1295 increases GH synthesis while Ipamorelin triggers its release — resulting in substantially amplified GH output in combination protocols.
RESEARCH APPLICATIONS
KEY RESEARCH FINDINGS
STORAGE & HANDLING
SPECIFICATIONS
| CAS Number | 170851-70-4 |
| Molecular Formula | C38H49N9O5 |
| Molecular Weight | 711.85 Da |
| Appearance | White lyophilized powder |
| Purity | ≥99% (HPLC verified) |
| Available Strengths | 10 mg |
| Storage | -20°C (lyophilized), 2–8°C (reconstituted) |
| Solubility | Bacteriostatic water |
DISCLAIMER: This compound is sold strictly for laboratory and research purposes only. It is not intended for human consumption, clinical use, or veterinary application. These statements have not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease. For use by licensed researchers and qualified professionals only. You must be 21 years of age or older to purchase.
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