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Sermorelin 5mg
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Sermorelin 5mg (GRF 1-29)

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$34 USD
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Certificate of Analysis

Latest COA reported August 10, 2026.

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Purity / Result

>99.80% +/- 0.18%

Mass / Quantity

5.18 mg

Application formLyophilized powder
StorageRefrigerated
Purity98%
Weight5mg
CAS Number86168-78-7

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.

Sermorelin is one of a handful of GHRH analogues developed to preserve the positive effects of natural GHRH while avoiding undesirable effects. Currently used clinically to assess growth hormone secretion (Geref), it has demonstrated additional research promise in reducing cardiac remodeling and scar size following heart attack, suppressing seizures via GABA receptor activation, boosting orexin secretion for sleep regulation, and increasing bone density. Unlike exogenous growth hormone, sermorelin is subject to physiological feedback mechanisms and is not subject to tachyphylaxis, making it the preferred way to modulate GH levels in research settings. This 5mg vial provides material for initial endocrine research protocols.

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What Is Sermorelin?

Sermorelin is one of a handful of growth hormone releasing hormone (GHRH) analogues that have been developed in recent years in an effort to preserve some of the positive effects of natural GHRH while avoiding undesirable effects. Sermorelin (Geref) is currently used clinically to assess growth hormone secretion, but the peptide is of additional interest for its abilities to reduce scarring following heart attack, increase bone density, improve nutrition in chronic illness, improve renal function, fight the effects of dementia, and reduce seizure activity.

Sermorelin Peptide Structure

Sermorelin molecular structure
Amino Acid SequenceTyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg
Molecular FormulaC149H246N44O42S
Molecular Weight3357.933 g/mol
PubChem CID16129620

Sermorelin and Heart Health

Heart attack, while acutely life-threatening, can also lead to long-term disability secondary to heart failure, cardiac conduction abnormalities (arrhythmias), reduced exercise capacity, pain, and more. A number of these problems result from cardiac remodeling that follows damage to myocytes. In 2016, a study in pigs revealed that sermorelin administration is effective in reducing the remodeling that follows a heart attack. The research showed that sermorelin reduces cell death in cardiomyocytes, increases the production of extracellular matrix components needed for adequate healing, increases the growth of blood vessels to damaged tissue, and reduces the production of substances that cause damaging inflammation. Clinically, sermorelin's effects are seen in improved diastolic function, reduced scar size, and increased capillary growth[1], [2].

Sermorelin and Epilepsy

GABA is a central nervous system signaling molecule known to reduce electrical activity in the spinal cord and reduce overall electrical excitability in the central nervous system. In a recent study of mice with epilepsy, scientists administered GHRH analogues, like sermorelin, to test the effect of these peptides on seizure activity. It turns out that GHRH analogues are effective in suppressing seizures by activating GABA receptors[3].

Sermorelin and Sleep

There is good evidence that sleep cycles are regulated by orexin, a potent neurochemical produced by certain neurons in the brain. Research in rainbow trout suggests that an intact GHRH axis is a necessary component for proper orexin secretion and function. In addition, the research reveals that exogenous administration of sermorelin and other GHRH agonists can boost orexin secretion[4].

Sermorelin Preferred to Growth Hormone

Sermorelin is the preferred way to increase GH levels, even over exogenous GH itself. The primary reason is that sermorelin is subject to physiological feedback mechanisms that help prevent common problems like overdose, improper dosing, and unintended side effects like edema, joint pain, and dysregulation of normal physiology[5].

A second reason is that research shows it is not subject to tachyphylaxis. Rather than down-regulate the production of GHRH receptors, the body instead increases their production[6].

Sermorelin Summary

Sermorelin exhibits moderate side effects, low oral and excellent subcutaneous bioavailability in mice. Per kg dosage in mice does not scale to humans. Sermorelin for sale at Volta Peptides is limited to educational and scientific research only.

Article Author

The above literature was researched, edited and organized by Dr. E. Logan, M.D. Dr. E. Logan holds a doctorate degree from Case Western Reserve University School of Medicine and a B.S. in molecular biology.

Scientific Journal Author

Richard F. Walker holds a B.S. in pharmacy from Rutgers University, an M.S. in Biochemistry from New Mexico State University, and a Ph.D. in physiology from Rutgers University. He completed postdoctoral fellowships at Duke University and the University of California, Berkeley.

Referenced Citations

  1. 1L. L. Bagno et al., "Growth Hormone-Releasing Hormone Agonists Reduce Myocardial Infarct Scar in Swine With Subacute Ischemic Cardiomyopathy," J. Am. Heart Assoc., vol. 4, no. 4, Mar. 2015.
  2. 2R. M. Kanashiro-Takeuchi et al., "New therapeutic approach to heart failure due to myocardial infarction based on targeting growth hormone-releasing hormone receptor," Oncotarget, vol. 6, no. 12, pp. 9728-9739, Mar. 2015.
  3. 3S. Tang et al., "Interactions between GHRH and GABAARs in the brains of patients with epilepsy and in animal models of epilepsy," Sci. Rep., vol. 7, Dec. 2017.
  4. 4B. S. Shepherd et al., "Endocrine and orexigenic actions of growth hormone secretagogues in rainbow trout," Comp. Biochem. Physiol., vol. 146, no. 3, pp. 390-399, Mar. 2007.
  5. 5R. F. Walker, "Sermorelin: A better approach to management of adult-onset growth hormone insufficiency?," Clin. Interv. Aging, vol. 1, no. 4, pp. 307-308, Dec. 2006.
  6. 6S. T. Wahid et al., "Partial tachyphylaxis to somatostatin analogues in a patient with acromegaly," Eur. J. Endocrinol., vol. 146, no. 3, pp. 295-302, Mar. 2002.

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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