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Research-grade peptides for laboratory and in-vitro research. Third-party tested, documented per batch.

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!FDA Disclaimer — Research Use Only

Statements regarding these products have not been evaluated by the U.S. Food and Drug Administration. These products are intended for laboratory and in-vitro research use only and are not for human or veterinary consumption of any kind. They are not drugs, foods, or supplements, are not FDA approved, and are not intended to diagnose, treat, cure, or prevent any disease. All products are sold exclusively to qualified researchers and must be handled by trained professionals. Read the full disclaimer →

© 2026 Luvaminos LLC. All products for research purposes only. Not for human consumption. Not FDA approved.

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Research/Ipamorelin

GH Secretagogue

Ipamorelin

A selective secretagogue peptide studied in preclinical research.

What It’s Studied For

Ipamorelin is studied for how the body releases its own growth hormone. It is a small, highly selective peptide that activates the ghrelin receptor on the pituitary gland, and it is used as a selective probe in preclinical growth-hormone-secretion research.

Molecular Profile

Type

Synthetic peptide (pentapeptide)

Molecular formula

C38H49N9O5

Molecular weight

711.9 g/mol

CAS number

170851-70-4

Amino acids

5

Sequence

Aib-His-D-2-Nal-D-Phe-Lys-NH2

Modification

N-terminal Aib; D-2-naphthylalanine; D-Phe; C-terminal amide.

Mechanism & Target Class

A synthetic pentapeptide that binds the growth-hormone secretagogue receptor (GHS-R1a / ghrelin receptor), a class A GPCR on pituitary somatotrophs. It does not bind the GHRH receptor.

Research Focus

Studied in GHS-R1a receptor pharmacology and growth-hormone-secretion research.

Storage & Handling

Lyophilized

-20°C

typically stable 24-36 months desiccated and protected from light.

Reconstituted

2-8°C for short-term use

-20°C/-80°C for longer storage.

Avoid freeze-thaw; aliquot; protect from light and moisture.

References

Clinical

  1. 1

    Beck DE, et al. (2014). Int J Colorectal Dis — Phase 2 trial in postoperative ileus (bowel-resection patients)

    DOI: 10.1007/s00384-014-2030-8PubMed 25331030
  2. 2

    Gobburu JVS, et al. (1999). Pharm Res — PK/PD modeling study in healthy volunteers

    DOI: 10.1023/A:1018955126402PubMed 10496658

Primary research

  1. 3

    Greenwood-Van Meerveld B, et al. (2012). J Exp Pharmacol — Rodent postoperative-ileus model

    DOI: 10.2147/JEP.S35396PubMed 27186127
  2. 4

    Venkova K, et al. (2009). J Pharmacol Exp Ther — Rodent postoperative-ileus model

    DOI: 10.1124/jpet.108.149211PubMed 19289567
  3. 5

    Adeghate E, Ponery AS. (2004). Neuro Endocrinol Lett — Pancreatic insulin-release mechanism study (rat tissue)

    PubMed 15665799
  4. 6

    Jiménez-Reina L, et al. (2002). Histol Histopathol — Somatotroph-responsiveness study (young female rats)

    DOI: 10.14670/HH-17.707PubMed 12168778
  5. 7

    Svensson J, et al. (2000). J Endocrinol — Bone-mineral-endpoint study (adult female rats)

    DOI: 10.1677/joe.0.1650569PubMed 10828840
  6. 8

    Malmlöf K, et al. (2000). Growth Horm IGF Res — GH-release study under glucocorticoid conditions (rats)

    DOI: 10.1054/ghir.1999.0128PubMed 10629165
  7. 9

    Johansen PB, et al. (1999). Growth Horm IGF Res — Longitudinal bone-growth study (rats)

    DOI: 10.1054/ghir.1999.9998PubMed 10373343
  8. 10

    Raun K, et al. (1998). Eur J Endocrinol — Foundational secretagogue-characterization study

    DOI: 10.1530/eje.0.1390552PubMed 9849822

Primary Database

PubChem CID 9831653↗

Research Use Only

These products are intended for research purposes only and are not for human consumption. Not FDA approved. Not intended to diagnose, treat, cure, or prevent any disease.