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-1a). By binding to this receptor in the pituitary and hypothalamus, it stimulates pulsatile growth hormone (GH) release, leading to sustained elevations in insulin-like growth factor 1 (IGF-1) levels for up to 24 hours following a single dose. Unlike exogenous GH administration, MK-677 preserves the endogenous feedback regulation of the GH/IGF-1 axis. Key research findings from clinical trials indicate that MK-677 increases GH and IGF-1 levels in a dose-dependent manner without significantly altering cortisol or prolactin. Studies have shown improvements in lean body mass, bone mineral density, and muscle strength in elderly populations, as well as potential benefits in conditions such as frailty, sarcopenia, and growth hormone deficiency. However, transient increases in fasting glucose and insulin resistance have been observed, suggesting a need for careful metabolic monitoring. Clinically, MK-677 has been investigated for age-related decline in GH secretion, muscle wasting disorders, and as an adjunct to fracture healing. Despite promising anabolic effects, its development has been limited by metabolic side effects and lack of long-term safety data. It remains an investigational compound with no approved therapeutic indications. 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-1a). By binding to this receptor in the pituitary and hypothalamus, it stimulates pulsatile growth hormone (GH) release, leading to sustained elevations in in
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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