Hexarelin
Examorelin
Synthetic growth hormone secretagogue (GHRP class). Not FDA-approved; human data limited.
Oral, non-peptide ghrelin receptor agonist. Not FDA-approved; investigational.
MK-677 (ibutamoren) is an orally bioavailable small-molecule ghrelin receptor agonist developed by Merck in the 1990s. Despite often being grouped with peptide GH secretagogues, MK-677 is technically not a peptide — it is a synthetic small molecule that mimics ghrelin’s effects on the GH-releasing pathway.
MK-677 was studied by Merck in the 1990s and 2000s for GH deficiency, frailty in elderly populations, and other indications. The development program was eventually discontinued. The compound was later licensed to other companies for development in pediatric GH deficiency, but has not received FDA approval for any indication. MK-677 is not FDA-approved for any use in the United States.
Proposed mechanisms come from laboratory, animal, and early human research. MK-677 acts as a ghrelin receptor (GHS-R1a) agonist:
MK-677 was evaluated in clinical trials during the Merck development program:
Well-controlled human trials establishing effectiveness and safety for any use are lacking, and the compound has not been approved.
The Tide does not prescribe or offer MK-677. Concerns noted in the research literature include:
Human safety has not been established for long-term use. Reported effects include increased appetite, fluid retention, joint discomfort, fatigue, and reduced insulin sensitivity, and sustained GH/IGF-1 elevation raises concerns about growth-promoting signaling in people with cancer. Products sold outside regulated channels (for example, as “research chemicals”) may vary in purity, dose, and identity.
Examorelin
Synthetic growth hormone secretagogue (GHRP class). Not FDA-approved; human data limited.
GRF 1-29
Synthetic GHRH analog (GRF 1-29). Previously FDA-approved as Geref; the brand product was discontinued. Current US supply is compounded and not FDA-approved.
Modified GRF 1-29 (no DAC)
Synthetic GHRH analog (modified GRF 1-29). Not FDA-approved; human data limited to early studies.