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Ipamorelin 10mg
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Ipamorelin 10mg — Research Grade Peptide

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$49 USD
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Certificate of Analysis

Latest COA reported June 20, 2026.

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Purity / Result

99.07% average

Mass / Quantity

9.94 mg average

Application formLyophilized powder
StorageRefrigerated
Purity98%
Weight10mg
CAS Number170851-70-4

Research Use Only

For in vitro laboratory research by qualified professionals only. Not for human or animal administration. Not intended to treat, prevent, mitigate, or cure any disease. Batch-specific Certificates of Analysis available for all products.

Ipamorelin is a short peptide sequence capable of binding to the ghrelin/growth hormone secretagogue receptor with exceptional selectivity. Research demonstrates its ability to completely stop bone loss due to corticosteroids and even lead to a four-fold increase in bone formation, while also increasing bone mineral density systemically. Studies indicate ipamorelin reduces nitrogen wasting in the liver and improves nitrogen balance, counteracting the catabolic effects of glucocorticoids on muscle. It potentiates insulin release through indirect stimulation of calcium channels on pancreatic islet cells. Ipamorelin has also been investigated for reducing post-operative ileus, shortening time to first meal by approximately 12 hours, and shows promise as a PET probe for diagnosing cancers and heart failure via its ghrelin receptor binding. This 10mg vial provides ample material for comprehensive GH-axis modulation research.

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What Is Ipamorelin?

Ipamorelin is a short peptide sequence capable of binding to the ghrelin/growth hormone secretagogue receptor. It is one of the most selective growth hormone (GH) secretagogues known and has been shown in laboratory studies to have no effect on ACTH, prolactin, follicle-stimulating hormone, luteinizing hormone, thyroid-stimulating hormone, or cortisol release[1]. Given its high level of specificity, ipamorelin has been of interest in research both as a therapeutic in and of itself as well as a model peptide for understanding how selectivity in receptor binding is achieved.

Ipamorelin Structure

Ipamorelin Peptide Structure
SequenceAib-His-D-2Nal-D-Phe-Lys
Molecular FormulaC38H49N9O5
Molecular Weight711.868 g/mol
PubChem CID9831659
CAS Number170851-70-4

Ipamorelin and Negative Corticosteroid Effects

Glucocorticoids, the class of corticosteroids commonly used to treat inflammation in conditions ranging from cancer to autoimmune disease, have a host of serious side effects that often limit their usefulness. Mitigating the side effects of glucocorticoids could provide for higher dosing of these medications and allow people to remain on them for longer periods of time, both of which could have positive benefits on morbidity and mortality. Ipamorelin has been shown, in several studies, to reduce or even reverse the side effects of glucocorticoid use.

Ipamorelin and Bone Health

One of the most profound problems associated with long-term glucocorticoid use is loss of bone density and subsequent risk of fracture. Current therapies include bisphosphonates, hormone therapies, and new monoclonal antibodies. All of these are effective treatments in their own rights, but they also all have side effects, limited efficacy, or high cost. Ipamorelin, on the other hand, is relatively inexpensive to produce and has a very limited number of side effects.

Studies in rats indicate that ipamorelin can completely stop bone loss due to corticosteroids and even leads to a four-fold increase in bone formation in rats exposed to these drugs[2]. Further studies indicate that ipamorelin also increases bone mineral density systemically, thereby increasing the strength of both existing bone and newly formed bone[3]. As an added bonus, ipamorelin helps to offset some of the other side effects of steroids, such as muscle wasting and increased visceral fat deposition.

Ipamorelin and Muscle Growth

There is evidence to suggest that GH and growth hormone secretagogues like ipamorelin may reduce the catabolic effects that glucocorticoids have on muscle. Research in rats given glucocorticoids shows a decrease in nitrogen wasting in the liver and improved nitrogen balance following administration of ipamorelin[4]. Muscle wasting is one of the primary side effects associated with glucocorticoid use and a common treatment-limiting side effect. The ability to counteract muscle catabolism and bone-density loss with a single drug could be hugely beneficial to patients who require glucocorticoids.

Ipamorelin and Diabetes

Research in diabetic rats has revealed that ipamorelin can potentiate insulin release. This effect is most likely a result of indirect stimulation of the calcium channel found on pancreatic islet cells where insulin is made and stored[5]. Ipamorelin's actions on the pancreas may help us better understand the functional limitations of type 2 diabetes and lead to the development of novel therapeutics or even preventative measures.

Ipamorelin and Post-Operative Ileus

Post-operative ileus (POI) is a common condition that follows certain types of surgery, but is particularly common following abdominal surgery. The condition is characterized by an inability of individuals to take oral nutrition because the GI system ceases to function. It can be characterized by pain, but the primary problem with POI is that it slows discharge from the hospital and lengthens overall recovery time.

Ipamorelin has been investigated in several proof-of-concept clinical trials to determine if administration of the peptide can reduce POI. The research suggests that ipamorelin does shorten time to first meal by approximately 12 hours[6], [7].

Ipamorelin Studied for Treatment of Post-Operative Ileus
Ipamorelin reduces gastric dysmotility in rodent models of post-operative ileus. Source: PubMed

Ipamorelin as Ghrelin Receptor Probe

Ipamorelin is a selective ghrelin receptor agonist and binds strongly to the ghrelin receptor. The ghrelin receptor is known to increase in abundance in certain types of cancer (e.g. human carcinomas) and heart failure. Given these facts, researchers recently speculated that ipamorelin could be used as a probe in positron emission tomography (PET) as an aid to diagnosis.

Basic in vitro studies have demonstrated the feasibility of this approach and have confirmed that ipamorelin[8], which is easy to synthesize in a lab, could theoretically be used as a PET probe.

Ipamorelin Research Summary

Ipamorelin exhibits moderate side effects, low oral and excellent subcutaneous bioavailability in mice. Per kg dosage in mice does not scale to humans. Ipamorelin for sale at Volta Peptides is limited to educational and scientific research only, not for human consumption. Only buy Ipamorelin if you are a licensed researcher.

Article Author

Dr. Logan holds an M.D. from Case Western Reserve University School of Medicine and a B.S. in molecular biology. His research interests span endocrinology, peptide therapeutics, and growth hormone physiology.

Scientific Journal Author

David E. Beck, MD is the co-author of "Prospective, randomized, controlled, proof-of-concept study of the Ghrelin mimetic ipamorelin for the management of postoperative ileus in bowel resection patients." He specializes in colon and rectal surgery and has contributed extensively to research on gastrointestinal recovery following surgical procedures.

Referenced Citations

  1. 1K. Raun et al., "Ipamorelin, the first selective growth hormone secretagogue," Eur. J. Endocrinol., vol. 139, no. 5, pp. 552-561, Nov. 1998.
  2. 2N. B. Andersen et al., "The growth hormone secretagogue ipamorelin counteracts glucocorticoid-induced decrease in bone formation of adult rats," Growth Horm. IGF Res., vol. 11, no. 5, pp. 266-272, Oct. 2001.
  3. 3J. Svensson et al., "The GH secretagogues ipamorelin and GH-releasing peptide-6 increase bone mineral content in adult female rats," J. Endocrinol., vol. 165, no. 3, pp. 569-577, Jun. 2000.
  4. 4N. K. Aagaard et al., "Growth hormone and growth hormone secretagogue effects on nitrogen balance and urea synthesis in steroid treated rats," Growth Horm. IGF Res., vol. 19, no. 5, pp. 426-431, Oct. 2009.
  5. 5E. Adeghate and A. S. Ponery, "Mechanism of ipamorelin-evoked insulin release from the pancreas of normal and diabetic rats," Neuro Endocrinol. Lett., vol. 25, no. 6, pp. 403-406, Dec. 2004.
  6. 6D. E. Beck et al., "Prospective, randomized, controlled, proof-of-concept study of the Ghrelin mimetic ipamorelin for the management of postoperative ileus in bowel resection patients," Int. J. Colorectal Dis., vol. 29, no. 12, pp. 1527-1534, Dec. 2014.
  7. 7B. Greenwood-Van Meerveld et al., "Efficacy of ipamorelin, a ghrelin mimetic, on gastric dysmotility in a rodent model of postoperative ileus," J. Exp. Pharmacol., vol. 4, pp. 149-155, Oct. 2012.
  8. 8M. M. Fowkes et al., "Peptidomimetic growth hormone secretagogue derivatives for positron emission tomography imaging of the ghrelin receptor," Eur. J. Med. Chem., vol. 157, pp. 1500-1511, Sep. 2018.

Disclaimer

All articles and product information provided on this website are for informational and educational purposes only. The products offered on this website are furnished for in-vitro studies only. These products are not medicines or drugs and have not been approved by the FDA to prevent, treat or cure any medical condition, ailment or disease.

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