Growth ⏱ Half-life: Approximately 24 hours, supporting once-daily oral administration. IGF-1 elevation persists throughout the 24-hour period.

MK-677

MK-677 (Ibutamoren Mesylate)

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Half-Life
Approximately 24 hours, supporting once-daily oral administration. IGF-1 elevation persists throughout the 24-hour period.
Mol. Weight
528.662 g/mol

What is MK-677?

MK-677 (Ibutamoren) occupies a unique position in GH-axis research as an orally bioavailable, non-peptide growth hormone secretagogue. While technically not a peptide, it acts on the same ghrelin receptor (GHS-R1a) as injectable GHRP peptides, making it functionally relevant to peptide research.

Research Applications

Clinical research areas: GH/IGF-1 axis stimulation (chronic oral dosing), sarcopenia and muscle wasting models, sleep architecture studies, bone mineral density research, and age-related GH decline.

Dosage Information (Research Use)

Published clinical trial doses: 10-25 mg once daily, oral administration, typically taken at bedtime. Duration up to 2 years in published studies. Research use only.

Reconstitution & Handling

N/A — MK-677 is an orally-active compound, not a reconstitutable peptide.

Half-Life & Pharmacokinetics

Approximately 24 hours, supporting once-daily oral administration. IGF-1 elevation persists throughout the 24-hour period.

Reported Observations in Literature

Published clinical data reports: increased appetite (pronounced), water retention, transient lethargy, numbness/tingling, elevated fasting glucose, and potential insulin resistance with chronic use.

Key Research References

  • Murphy MG, et al. “MK-677, an orally active growth hormone secretagogue, reverses diet-induced catabolism.” J Clin Endocrinol Metab. 1998
  • Nass R, et al. “Effects of an oral ghrelin mimetic on body composition and clinical outcomes in healthy older adults.” Ann Intern Med. 2008

How MK-677 Works

MK-677 (Ibutamoren) is a non-peptide, orally-active growth hormone secretagogue that mimics ghrelin at the GHS-R1a receptor. Despite not being a peptide, it is commonly discussed in peptide research contexts due to its action on the same receptor as GHRP peptides. Key distinction: MK-677 provides sustained 24-hour GH elevation (unlike injectable GHRPs which produce acute pulses), increases both GH pulse amplitude and frequency, and maintains its effects over long-term administration without significant tachyphylaxis.

Research Findings

Multiple clinical trials have been completed including 2-year administration studies. Research shows sustained IGF-1 elevation, improved sleep quality, and body composition changes. One of the few GH secretagogues with long-term human clinical data. Notable glucose metabolism effects — can increase fasting blood glucose and insulin resistance in some research subjects, requiring monitoring.

Dosage & Administration

Published clinical trial doses: 10-25 mg once daily, oral administration, typically taken at bedtime. Duration up to 2 years in published studies. Research use only.

Safety & Side Effects

Published clinical data reports: increased appetite (pronounced), water retention, transient lethargy, numbness/tingling, elevated fasting glucose, and potential insulin resistance with chronic use.

Important: All safety information is derived from published research, primarily animal studies. No controlled human clinical trial data exists unless explicitly noted. This compound is sold for research purposes only.

Quick Facts

Sequence Non-peptide (small molecule ghrelin mimetic)
Molecular Weight 528.662 g/mol
Half-Life Approximately 24 hours, supporting once-daily oral administration. IGF-1 elevation persists throughout the 24-hour period.
Available Sizes 25mg capsules, powder
Storage Room temperature, away from moisture and light.

Key Research References

  • Murphy MG, et al. "MK-677, an orally active growth hormone secretagogue, reverses diet-induced catabolism." J Clin Endocrinol Metab. 1998
  • Nass R, et al. "Effects of an oral ghrelin mimetic on body composition and clinical outcomes in healthy older adults." Ann Intern Med. 2008

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