Ipamorelin

Ipamorelin is a selective growth hormone secretagogue, specifically classified as a pentapeptide and belonging to the growth hormone-releasing peptide (GHRP) family. Unlike other GHRPs, Ipamorelin exhibits targeted specificity toward growth hormone (GH) release without significantly affecting cortisol or prolactin levels, making it an important tool for controlled, precise in vitro research conditions. Researchers frequently use Ipamorelin to examine growth hormone stimulation pathways, pulsatile GH secretion dynamics, and metabolic regulatory effects. It’s unique because it specifically targets growth hormone release without significantly affecting other hormones, such as stress hormones. Researchers use it in the lab to better understand how growth hormone works and how it affects things like metabolism, muscle growth, and overall body function.

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Description

Disclaimer: This is a research chemical only. It’s not a medication, and it’s not approved for human or animal use outside of authorized studies

Sequence Aib‑His‑D‑2‑Nal‑D‑Phe‑Lys‑NH₂ (Ipamorelin) 
Molecular Formula C₃₈H₄₉N₉O₅
Molecular Weight ~711.8 g/mol
PubChem CID 20754357
CAS # 1170851‑70‑4

Ipamorelin is a synthetic pentapeptide classified as a selective growth hormone secretagogue. It exerts its action through specific binding to the ghrelin (GHS-R1a) receptor, stimulating pulsatile secretion of endogenous growth hormone (GH) while exhibiting minimal influence on other pituitary hormones such as cortisol, ACTH, or prolactin.

In experimental settings, Ipamorelin is studied for its role in modulating GH–IGF-1 axis signaling, offering insight into downstream pathways involved in protein synthesis, cellular recovery, metabolic regulation, and musculoskeletal adaptation. Its receptor selectivity makes it a valuable investigative tool for differentiating the isolated effects of GH release from broader endocrine interactions typically triggered by non-specific secretagogues.

Pharmacologically, Ipamorelin demonstrates dose-dependent GH release with relatively low off-target activity, making it a preferred model compound in controlled laboratory studies examining endocrine feedback loops, tissue growth kinetics, and metabolic homeostasis.

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