
BPC-157
Stable gastric pentadecapeptide, a staple of tissue-repair research.

Selective ghrelin-receptor agonist for GH-release research.
Ipamorelin 10 mg
Your order ships with the certificate for its own lot. 1 earlier certificate for this size in the COA library.
Selective ghrelin-receptor agonist for GH-release research.
10 mg per vial, as a lyophilized powder in a sealed glass vial with a crimped cap. The lot number on the label matches the certificate of analysis in the COA library.
Store lyophilized powder frozen (−20 °C) or refrigerated, sealed and away from light. Once reconstituted, keep refrigerated (2–8 °C).
Handle in a laboratory setting using appropriate protective equipment. Consult the certificate of analysis and safety data for lot-specific information.
Ipamorelin is a synthetic pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2) that releases growth hormone (GH) by activating the growth hormone secretagogue receptor, the receptor for the stomach hormone ghrelin. Novo Nordisk researchers described it in 1998 as the first selective GH secretagogue because, in swine, it raised GH without the ACTH and cortisol increases seen with GHRP-2 and GHRP-61. It reached a phase 2 trial for postoperative ileus but is not an approved medicine2; it is sold for laboratory research only.
Ipamorelin came out of a medicinal chemistry program at Novo Nordisk, from a series of compounds lacking the central Ala-Trp dipeptide of GHRP-1. In primary rat pituitary cells it released GH with potency and efficacy similar to GHRP-6, and experiments with GHRP and GHRH antagonists showed that it works through the GHRP-type receptor rather than the GHRH receptor1. In early pharmacokinetic work it carried the code NNC 26-01613.
That receptor, the growth hormone secretagogue receptor (GHS-R), was cloned in 1996 as a G protein-coupled receptor of the pituitary and hypothalamus4. In 1999 its natural ligand was identified as ghrelin, a 28-amino-acid acylated peptide from the stomach5. Ipamorelin is therefore described as a ghrelin-receptor agonist or ghrelin mimetic6.
Earlier GH-releasing peptides also raise other pituitary and adrenal hormones. In conscious swine, GHRP-6 and GHRP-2 both increased plasma ACTH and cortisol, whereas ipamorelin did not raise either beyond the levels seen after GHRH stimulation, even at more than 200 times the amount needed for half-maximal GH release. None of the secretagogues tested changed FSH, LH, prolactin or TSH1.
That selectivity was shown in specific animal models over short experiments. It explains why ipamorelin is chosen when researchers want GHS-R activation with little adrenal-axis signal; it is not evidence about long-term effects in people.
Ipamorelin and GHRH analogues such as sermorelin and CJC-1295 without DAC act on the same pituitary cells through different receptors. In healthy men, a GH-releasing hexapeptide given together with GHRH released GH synergistically, which the authors took as evidence that the two pathways act independently11. That body of work is why the two classes are studied together, as in the CJC-1295 + Ipamorelin vial. Our article Ipamorelin vs Sermorelin vs Tesamorelin compares them in detail.
It descends from the GHRP family, coming from a series built on GHRP-1, and like GHRP-6 it acts at the GH secretagogue (ghrelin) receptor1. It is a pentapeptide, one residue shorter than the hexapeptide GHRPs.
No. It was evaluated in a phase 2 trial for postoperative ileus that did not show a significant difference from placebo2, and it has not been approved for any use.
Sermorelin is a fragment of GHRH and acts at the GHRH receptor; ipamorelin is a synthetic ghrelin-receptor agonist1,4. Both lead to GH release from the same pituitary cells, but through separate receptors.
In healthy volunteers who received it by intravenous infusion, the terminal half-life was about 2 hours7.
In the original swine studies it did not raise ACTH or cortisol beyond the levels seen with GHRH, unlike GHRP-2 and GHRP-61. Long-term human data on this point do not exist.
Research summary reviewed 2026-10-26 against the cited literature.

Stable gastric pentadecapeptide, a staple of tissue-repair research.

Copper-binding tripeptide used in collagen and skin-matrix research.

Essential coenzyme for studies of cellular metabolism and ageing.

Thymosin beta-4 fragment studied for cell migration and repair.
Operated by DND Wellness LLC · 1309 Coffeen Ave, Suite 1200, Sheridan, WY 82801.
support@peptides-only.com · (508) 404-8124
Use the chat widget to ask a question. Informational and promotional text messages require separate, optional consent. Message frequency varies. Msg & data rates may apply. Reply STOP to unsubscribe or HELP for help. Consent is not a condition of purchase. 21+.
SMS consent & support · SMS terms & Terms of Service · Privacy Policy