GHRP-6
/ Synthetic hexapeptide; ghrelin / GHS-R1a receptor agonist; first characterized GHRPTerms in this page you can click for a plain-English popup: , , , , , , , .
Historical first-generation growth hormone-releasing peptide. Not in modern pharmaceutical development. Substantial appetite stimulation and cortisol/prolactin side effects.
GHRP-6 was one of the first characterized synthetic growth hormone-releasing peptides (Bowers 1984). It acts at the ghrelin/GHS-R1a receptor but is notable for pronounced appetite stimulation — a direct reflection of ghrelin-mimetic activity.
Foundational pharmacology studies exist; no ongoing pharmaceutical development. Largely superseded by ipamorelin (selective) and MK-677 (oral) in modern GH-secretagogue research.
Pronounced appetite stimulation. Cortisol and prolactin elevation. Flushing. No long-term human safety data at chronic doses. Limited modern human safety evaluation.
Regulatory status
- FDA status:
- Not FDA-approved
GHRP-6 is historically important but largely obsolete in current GH-secretagogue research. Its continued presence in the research-chemical market reflects commodity production rather than scientific priority.