Overview
MK-677 is a small-molecule ghrelin-receptor agonist developed by Merck. It is technically a peptidomimetic rather than a true peptide, but it shares mechanism with the GHRPs.
- Synthesized in research laboratories
- Oral capsule or solution
Mechanism of action
Binds GHS-R1a like the GHRPs but is orally bioavailable and long-acting, producing sustained nightly GH and IGF-1 elevation.
- · GHS-R1a activation
- · Somatostatin suppression
- · GHS-R1a
- · GH
- · IGF-1
- · Cortisol
How it acts on the body
MK-677 mimics ghrelin at GHS-R1a but is structurally a small molecule with a 24-hour half-life, so a single oral dose produces an entire night of amplified GH pulses rather than a short spike. Over weeks, IGF-1 rises substantially and stays there.
The trade-offs are the same as ghrelin itself: meaningful appetite increase, water retention, mild insulin resistance, and occasional numbness in extremities from nerve-related water shifts. Effects on cortisol and prolactin are smaller than with the injectable GHRPs but not zero.
Hormonal & endocrine impact
How this peptide is reported to shift specific hormones and signaling molecules. Directionality reflects research literature and preclinical models, not clinical prescribing data.
Curves are schematic shapes (sigmoid for increases/decreases, damped oscillation for modulation/stabilization) anchored to a 100% baseline. They communicate direction and tempo of change reported in research literature — not absolute hormone concentrations.
Effects on the body
Organ system effects
Sustained pituitary GH / IGF-1 drive.
Appetite and sleep-architecture changes.
Increased gastric motility.
Reported effects
Drawn from preclinical research, anecdote, and small-scale clinical observation. No evidence grades are assigned — most peptides on this page lack rigorous human trials.
- Sleep-quality improvements
- Increased recovery markers
- Bone-density signals in trials
Potential side effects
- · Hunger
- · Water retention
- · Tingling
- · Lethargy
- · Vivid dreams
- · Glucose dysregulation
- · Heart-failure exacerbation in elderly trial subjects
Drug interactions
Pairing context
- Resistance training and adequate proteinAnabolic context for sustained IGF-1.
- Heart failure or active cancerDocumented worsening / theoretical risk.