MK-677 (Ibutamoren)
clinical trialsAlso known as: Ibutamoren, MK-0677, L-163,191
MK-677 (Ibutamoren) is an orally active, non-peptide ghrelin receptor agonist that mimics the action of ghrelin on the growth hormone secretagogue receptor (GHSR). By binding to this receptor in the pituitary and hypothalamus, it stimulates the pulsatile release of growth hormone (GH), leading to a sustained elevation of insulin-like growth factor 1 (IGF-1) levels for up to 24 hours per dose. Unlike exogenous GH administration, MK-677 preserves the natural feedback regulation of the GH/IGF-1 axis, though it does not significantly increase cortisol or prolactin levels in most studies. Key research findings from clinical trials indicate that MK-677 can increase lean body mass, improve bone mineral density, and enhance muscle strength in elderly or growth hormone-deficient populations. Studies have also shown improvements in sleep quality and a reduction in visceral adiposity. However, transient increases in fasting glucose and insulin resistance have been observed, particularly in older or metabolically compromised individuals, suggesting a potential risk for glucose intolerance with long-term use. Clinically, MK-677 has been investigated for conditions such as frailty, sarcopenia, and growth hormone deficiency, though it has not received FDA approval for any indication. Its ability to elevate GH and IGF-1 without injection offers a practical advantage over traditional GH therapy, but the metabolic side effects and lack of long-term safety data limit its clinical adoption. Further research is needed to clarify its risk-benefit profile in specific patient populations. For research purposes only — not medical advice.
Key data
C27H36N4O5SFrequently asked questions
What is MK-677 (Ibutamoren)?
MK-677 (Ibutamoren) is an orally active, non-peptide ghrelin receptor agonist that mimics the action of ghrelin on the growth hormone secretagogue receptor (GHSR). By binding to this receptor in the pituitary and hypothalamus, it stimulates the pulsatile release of growth hormone (GH), leading to a sustained elevation
How does MK-677 (Ibutamoren) work?
Orally active non-peptide ghrelin mimetic that sustains elevated GH and IGF-1 levels for 24 hours per dose.
What is the research status of MK-677 (Ibutamoren)?
MK-677 (Ibutamoren) is currently classified as clinical trials. This is for research purposes only and is not medical advice.
What is the half-life of MK-677 (Ibutamoren)?
The reported half-life of MK-677 (Ibutamoren) is ~24 hours.
What is the molecular weight of MK-677 (Ibutamoren)?
MK-677 (Ibutamoren) has a molecular weight of approximately 528.7 g/mol (formula C27H36N4O5S).
Related peptides
Endogenous cyclic peptide that inhibits GH, insulin, glucagon, and gastric secretion via SSTR1-5 receptors.
Endogenous 28-aa 'hunger hormone' from the stomach; activates GHS-R1a to stimulate GH release and appetite.
First-generation ghrelin receptor agonist hexapeptide that stimulates GH release and strongly increases appetite.
Potent GHRP-family ghrelin receptor agonist with studied cardioprotective effects independent of GH release.
Synthetic hexapeptide ghrelin receptor agonist that potently stimulates GH secretion; also raises appetite, cortisol, and prolactin.
Stabilized GHRH analog approved for HIV-associated lipodystrophy; reduces visceral adipose tissue via GH/IGF-1 axis stimulation.
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