GH Secretagogues

GHRP-6

Molecular Identifiers

Molecular Formula

C46H56N12O6

CAS Number

87616-84-0

PubChem CID

4345065

Molecular Weight

873.01 Da

Overview

First-generation GH-releasing peptide with strong ghrelin activity. Causes significant appetite increase. Potent GH release.

GHRP-6 drives potent endogenous GH release via high-affinity GHS-R1a receptor agonism, but with a strong ghrelinergic component and intense appetite increase, a feature that historically tied it to weight-gain and bulking protocols. Higher doses can raise cortisol and prolactin, which limits prolonged use.

GHRP-6 has no regulatory approval from any agency (FDA, EMA, ANVISA). It is typically dispensed by compounding pharmacies as off-label use in 8–12 week protocols, in up to three subcutaneous administrations per day (morning, post-workout, bedtime), often combined with GHRH analogs. It has gradually been replaced by more selective options such as GHRP-2 and ipamorelin. GH secretagogues are banned by WADA at all times.

It is one of the first GH-releasing peptides developed from synthetic hexapeptide libraries in the late 1980s, before ghrelin was identified as the endogenous ligand of GHS-R1a.

Among the GHRPs, GHRP-6 is the most ghrelinergic, with appetite stimulation markedly greater than GHRP-2 or hexarelin and in contrast to the selective profile of ipamorelin (no increase in appetite, cortisol, or prolactin). Compared to GHRH analogs (sermorelin, CJC-1295, tesamorelin) it acts on GHS-R1a rather than the GHRH receptor and is often paired with one of them; oral MK-677 reaches the same receptor with a 24-hour duration and preserves the appetite effect.

Extended notation: His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂

Contains D-amino acids (D-Trp, D-Phe)

Half-life

~15-20 minutes

Administration Route

Subcutaneous

Category

GH Secretagogues

Mechanism of Action

  • High-affinity GHS-R1a receptor agonist
  • Strong ghrelinergic activity (significant appetite increase)
  • Potent GH release
  • May elevate cortisol and prolactin at high doses

Dosage Protocol

Data compiled from the literature. This does not constitute medical advice.

Parameter Value
Dose 100-300 mcg per injection
Frequency 2-3 times per day
Timing Morning, post-workout and before bedtime
Duration 8-12 weeks

Reported Side Effects

Adverse effects described in the literature. Severity and frequency vary between individuals.

  • Intense appetite increase
  • Water retention
  • Elevated cortisol
  • Lethargy

Product Properties

Purity >99%
Appearance White lyophilized powder
Solubility Soluble in water and bacteriostatic water
Source Solid-phase peptide synthesis (SPPS)
Storage Lyophilized: -20°C for up to 2 years, 2-8°C for up to 6 months. Reconstituted: 2-8°C for up to 4 weeks. Protect from light and moisture. Avoid repeated freeze-thaw cycles.

Presentations & Preparation

Vials of GHRP-6 found in the research market:

5 mg10 mg

Reconstitution

  • Diluent: Bacteriostatic water
  • Volume: 2 ml per 5 mg vial
  • Inject the diluent slowly against the vial wall
  • Gently swirl until fully dissolved
  • Never shake

Storage

  • Lyophilized: Room temperature or refrigerated
  • Reconstituted: Refrigerated 2-8°C (up to 30 days)
  • Protect from direct light
  • Do not freeze after reconstitution
Reconstitution Calculator

Scientific Studies

Published studies on GHRP-6.

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