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Comparison · Growth-hormone secretagogues

Ipamorelin vs MK-677

Both stimulate growth-hormone release via the ghrelin receptor, but the similarity ends there. Here's how Ipamorelin (peptide, injectable, short half-life) and MK-677 (oral, ~24 h half-life) actually differ in research.

At a glance

AttributeIpamorelinMK-677
ClassPentapeptideOral small molecule
TargetGHSR-1aGHSR-1a
Half-life~2 hours~24 hours
RouteSubcut. injection (research)Oral
Cortisol / prolactinMinimalSome appetite / water retention

Mechanism

Both compounds bind the ghrelin receptor (GHSR-1a) on somatotrophs in the anterior pituitary, triggering a pulsatile growth-hormone release. Ipamorelin is selective and short-acting; MK-677 produces a sustained, day-long elevation of GH and IGF-1 in published studies.

Half-life & dosing pattern

Ipamorelin's ~2-hour half-life makes it suited to multiple daily doses or once-nightly use timed to natural GH pulses. MK-677's ~24-hour half-life enables once-daily oral dosing.

Research applications

Ipamorelin is favoured in research where investigators want a clean, ghrelin-receptor-selective probe without confounding cortisol or prolactin movement. MK-677 is favoured where chronic, steady IGF-1 elevation is the variable under study.

Side-effect signal in literature

Ipamorelin shows minimal cortisol/prolactin effects in published research. MK-677 has documented appetite stimulation (via ghrelin pathway), mild water retention and possible insulin sensitivity shifts in longer-term studies.

Frequently asked questions

Are Ipamorelin and MK-677 the same class?+

Both are growth-hormone secretagogues acting on the ghrelin receptor (GHSR-1a), but Ipamorelin is a peptide and MK-677 is an oral small molecule with very different pharmacokinetics.

Which has the longer half-life?+

MK-677 has a half-life of ~24 hours allowing once-daily dosing in studies; Ipamorelin is ~2 hours and is typically dosed multiple times per day in research protocols.

Does either raise cortisol or prolactin?+

Ipamorelin is notable for minimal effects on cortisol and prolactin in published research; MK-677 has shown some appetite and water-retention effects via ghrelin signalling.

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