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MONOGRAPH No. 022
SEQUENCE
His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂
MW
873.0 g/mol
CAS
87616-84-0
EU STATUS
Research only
WADA
Prohibited S2
MIN PURITY
≥98% HPLC
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⚡ Growth Hormone Axis

GHRP-6 — EU research guide.

GHRP-6 is a synthetic hexapeptide ghrelin mimetic and one of the first GH secretagogues developed. It stimulates GH release via GHS-R1a and is notable for its pronounced appetite-stimulating effects through ghrelin pathway activation.

Last reviewed:

What is GHRP-6?

GHRP-6 was among the first synthetic GH secretagogues characterised. It binds GHS-R1a in the hypothalamus and pituitary to stimulate GH release and also acts centrally via the orexigenic ghrelin pathway to powerfully stimulate appetite. This distinguishes it from Ipamorelin (appetite-neutral) and GHRP-2 (moderate appetite effect). The hexapeptide structure includes two D-amino acids for protease resistance.

What does the research show?

Extensive GH pharmacokinetics data in healthy subjects shows reliable GH pulses 15–60 minutes post-injection. In catabolic states, GHRP-6 shows protective effects on cardiac muscle and modulates inflammatory cytokines via a mechanism partially independent of GH release. The BPC-157 interaction with GHRP-6 in gut healing models has generated additional research interest.

EU legal status

Not approved in the EU. WADA-prohibited in sport (S2). Available for laboratory research only.

WADA-prohibited (S2). Strong appetite stimulation — ghrelin pathway activation. Cortisol and prolactin effects observed. Not for human use. This is a research compound, not a medication.
✓ PeptideCompare tracks GHRP-6 from EU vendors alongside Ipamorelin and GHRP-2. Compare GH secretagogue profiles before selecting for research.
EVIDENCE SUMMARY
MODERATE
GH secretion — The original GHRP; stimulates GH via the ghrelin receptor, with a weaker GH response than GHRP-2.
MODERATE (ANIMAL)
Appetite stimulation — Strong ghrelin-like appetite signal; studied in cachexia and wasting models.
LIMITED
Cardioprotection — Animal models suggest cardioprotective effects via the CD36 receptor; early-stage.

Molecular information

Molecular formula
C46H56N12O6
Molecular weight
873.0 g/mol
CAS number
87616-84-0

Pharmacokinetics

Route
Subcutaneous
Half-life (t½)
≈15–60 min
Source: GH-secretagogue pharmacology reviews
Research context only — not dosing guidance.

GHRP-6 across EU suppliers

COA-verified EU vendors · Updated monthly

Frequently asked questions

What is GHRP-6?

GHRP-6 was among the first synthetic GH secretagogues characterised. It binds GHS-R1a in the hypothalamus and pituitary to stimulate GH release and acts via the orexigenic ghrelin pathway to powerfully stimulate appetite.

Why does GHRP-6 increase appetite so strongly?

It acts centrally via the ghrelin pathway, which powerfully stimulates appetite, distinguishing it from appetite-neutral ipamorelin and the moderate effect of GHRP-2.

What does the research show?

Extensive GH pharmacokinetic data show reliable GH pulses 15 to 60 minutes post-injection, and in catabolic states it shows protective effects on cardiac muscle and modulates inflammatory cytokines partly independently of GH release.

What is the connection between GHRP-6 and BPC-157?

The interaction between GHRP-6 and BPC-157 in gut-healing models has generated additional research interest.

Is GHRP-6 legal in the EU?

It is not approved in the EU and is sold as a research compound for laboratory use only.

Is GHRP-6 banned in sport?

Yes. It appears on the WADA prohibited list (S2).

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