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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.

Reading this research reference

The information below concerns the research subject, not proof of the identity or performance of a supplied material. Check the original sources and your laboratory’s requirements; product documentation must be assessed separately for the exact batch.

At a glance

AttributeIpamorelinMK-677
ClassPentapeptideOral small molecule
TargetGHSR-1aGHSR-1a
Half-life~2 hours~24 hours
RouteLyophilised peptideOral
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

MK-677 has a reported half-life of around 24 hours.

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.

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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Ipamorelin on Bio Mech

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