Skip to main content
PepStack

Ipamorelin

GH Secretagogue
NNC 26-0161

Overview

Ipamorelin, also known as NNC 26-0161, is a synthetic peptide that functions as a growth hormone secretagogue. It is a pentapeptide with the sequence Aib-His-D-2-Nal-D-Phe-Lys-NH2, which was developed to mimic the effects of ghrelin, a natural hormone that stimulates growth hormone release. Researchers have synthesized Ipamorelin to explore its potential in various therapeutic applications, particularly those related to growth hormone deficiencies. The compound is typically synthesized using solid-phase peptide synthesis techniques. Researchers have primarily investigated Ipamorelin for its ability to stimulate the release of growth hormone from the pituitary gland. Studies have shown that it can increase growth hormone levels without significantly affecting cortisol or prolactin levels, which are often influenced by other secretagogues. This selective action makes Ipamorelin a subject of interest in the treatment of growth hormone deficiencies and related conditions. Additionally, its potential benefits in muscle growth and repair have been explored in preclinical studies. Ipamorelin acts by binding to the growth hormone secretagogue receptor (GHSR), which is a G-protein-coupled receptor. This interaction stimulates the release of growth hormone from the anterior pituitary gland. Unlike some other secretagogues, Ipamorelin does not significantly affect the release of other hormones such as cortisol, making it a more selective option for growth hormone stimulation. The pharmacokinetic properties of Ipamorelin include a relatively short half-life, with subcutaneous administration resulting in a half-life of approximately 2 hours. It is considered stable when stored appropriately, but its bioavailability can vary depending on the route of administration. Researchers have noted that oral bioavailability is poor, limiting its use to injectable forms. Current research on Ipamorelin is focused on its potential therapeutic applications, particularly in conditions involving growth hormone deficiencies. As of now, Ipamorelin is not approved for clinical use by major regulatory agencies, and its use is primarily restricted to research settings. It remains a compound of interest due to its selective action and potential benefits in muscle growth and repair.

Mechanism of Action

Ipamorelin binds to the growth hormone secretagogue receptor (GHSR), a G-protein-coupled receptor, leading to the stimulation of growth hormone release from the anterior pituitary gland. This selective binding does not significantly affect other hormones such as cortisol, making it a targeted growth hormone secretagogue.

Molecular Data

FormulaC38H49N9O5
Molecular Weight711.9 g/mol
CAS Number170851-70-4
PubChem CID9831659

Half-Life

Subcutaneous~2 hours
IntranasalNot applicable
OralPoor bioavailability

Ipamorelin's pharmacokinetics are characterized by a short half-life and limited oral bioavailability, necessitating injectable administration for effective use.

Storage

Lyophilized

Stable for 2+ years at -20°C, 12 months at 4°C

Reconstituted

Use within 14 days when refrigerated at 4°C

Avoid

Avoid repeated freeze-thaw cycles, direct light

Solvent

Bacteriostatic water or sterile saline recommended

Solubility

Ipamorelin is soluble in water and DMSO.

Legal Status

🇩🇪DE

Not approved as a medicinal product. Not a controlled substance. Sale as research chemical is a legal grey area.

🇺🇸US

Not approved by the FDA for clinical use. Not scheduled by the DEA.

🇦🇺AU

Not approved by the TGA for therapeutic use.

🇬🇧UK

Not approved by the MHRA for medicinal use.

Legal status information is provided for general reference only and may not reflect the most current regulatory changes. Always verify with official government sources before making any decisions.

7 Research Publications

Attenuation of Visceral and Somatic Nociception by Ghrelin Mimetics.

Animal

Journal of experimental pharmacology · 2020

Researchers observed that ghrelin mimetics, compounds that mimic the hormone ghrelin, can reduce visceral and somatic pain in a rat model without inflammation. The study indicates that these compounds may offer a new way to manage certain types of pain by acting on specific receptors in the body.

  • Ghrelin mimetics significantly reduced colonic hypersensitivity and somatic pain responses in rats.
  • The pain-relieving effects of these compounds were blocked when a ghrelin receptor antagonist was used.
  • This research suggests that targeting ghrelin receptors could be a novel approach for addressing acute pain.
PubMed

Analysis of new growth promoting black market products.

Unknown

Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society · 2018

Researchers studied new products on the black market that promote growth, focusing on human growth hormone (GH) and related peptides. They discovered a slightly modified form of GH and identified three new analogues of growth hormone releasing peptides (GHRPs). These findings highlight ongoing challenges in detecting these substances in sports drug testing.

  • Researchers observed a modified form of human growth hormone consisting of 192 amino acids.
  • They identified three new analogues of growth hormone releasing peptides (GHRPs) with an additional glycine residue.
  • The study utilized advanced mass spectrometry techniques to confirm the structures of these substances.
PubMed

Efficacy of ipamorelin, a novel ghrelin mimetic, in a rodent model of postoperative ileus.

Human

The Journal of pharmacology and experimental therapeutics · 2009

Researchers studied the effects of ipamorelin, a new drug that mimics ghrelin, on digestive recovery in rats after surgery. They found that ipamorelin reduced the time to the first bowel movement and increased overall food intake and body weight when given repeatedly, suggesting potential benefits for patients with postoperative ileus.

  • A single dose of ipamorelin decreased the time to the first bowel movement in rats after surgery.
  • Repetitive dosing of ipamorelin significantly increased food intake and body weight over 48 hours.
  • The study indicates that intravenous infusions of ipamorelin may improve digestive symptoms in patients recovering from surgery.
PubMed

Influence of chronic treatment with the growth hormone secretagogue Ipamorelin, in young female rats: somatotroph response in vitro.

Animal

Histology and histopathology · 2002

Researchers studied the effects of a substance called Ipamorelin on growth hormone-producing cells in young female rats. They found that chronic treatment with Ipamorelin increased the amount of growth hormone in these cells, suggesting that it can influence hormone production in the body.

  • Chronic treatment with Ipamorelin increased the volume of secretion granules in growth hormone cells.
  • The percentage of growth hormone cells increased after treatment with Ipamorelin and other growth hormone secretagogues.
  • Ipamorelin specifically enhanced the intracellular content of growth hormone in the treated cells.
PubMed

Ipamorelin, a new growth-hormone-releasing peptide, induces longitudinal bone growth in rats.

Human

Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society · 1999

Researchers studied a new peptide called ipamorelin and its effects on bone growth in rats. They found that ipamorelin increased the rate of bone growth and body weight in a dose-dependent manner, although it did not significantly affect certain hormone levels related to bone metabolism.

  • Ipamorelin increased the longitudinal bone growth rate in rats from 42 micrometers per day to 52 micrometers per day with higher doses.
  • The treatment also led to increased body weight gain in the rats.
  • Ipamorelin did not significantly alter levels of IGF-I or markers of bone formation and resorption.
PubMed

Pharmacokinetic evaluation of ipamorelin and other peptidyl growth hormone secretagogues with emphasis on nasal absorption.

Unknown

Xenobiotica; the fate of foreign compounds in biological systems · 1998

Researchers studied the absorption and clearance of three new growth hormone secretagogues, including ipamorelin, in male rats. They found that ipamorelin has a lower clearance rate compared to another peptide and shows promising nasal absorption, making it a potential candidate for systemic delivery.

  • Ipamorelin was excreted mainly in urine and had a systemic plasma clearance five times lower than GHRP-6.
  • After intranasal application, ipamorelin's bioavailability was about 20%, while other peptides had higher rates.
  • The study suggests that nasal delivery could be an effective method for administering these growth hormone secretagogues.
PubMed

A new series of highly potent growth hormone-releasing peptides derived from ipamorelin.

Animal

Journal of medicinal chemistry · 1998

Researchers studied new growth hormone-releasing peptides derived from ipamorelin to improve their effectiveness when taken orally. They found that one compound, NNC 26-0235, was highly effective in increasing growth hormone levels in animal models, showing promise for oral use.

  • NNC 26-0235 demonstrated comparable effectiveness to existing peptides when administered intravenously in animals.
  • This compound achieved 10% oral bioavailability in dogs, indicating potential for oral administration.
  • Another peptide, NNC 26-0323, showed moderate effectiveness in lab tests but had a higher oral bioavailability of 20% in rats.
PubMed

Track Ipamorelin in PepStack

Log your research cycles, set reminders and visualize serum levels.

This page is for informational and research purposes only. All information is based on published scientific literature. Nothing on this page constitutes medical advice or replaces consultation with a qualified healthcare professional.