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Muscle & performanceAnti-aging & longevity

GHRP-6

Growth Hormone Releasing Peptide-6 · SKF-110679

Early human trialsProhibited in sportReviewed 16 Aug 2026

GHRP-6 was the first synthetic growth hormone releasing peptide to be studied seriously, and much of what is known about the whole class was worked out with it. It binds the ghrelin receptor and produces a growth hormone pulse in the same way its relatives do.

What separates it is hunger. Ghrelin is the hormone that makes you hungry, and GHRP-6 mimics it more effectively than any other peptide in this family. For most people the appetite stimulation is not a mild side effect. It is the dominant experience of taking it, arriving within about twenty minutes and hard to ignore.

That has made GHRP-6 an odd compound in practice. People trying to gain weight sometimes want the hunger; people trying to lose it find the same effect makes the peptide unusable. Its other genuine research interest is cardiac and wound healing work — much of it Cuban — which is real literature but not the reason it is sold.

How it works

GHRP-6 activates the growth hormone secretagogue receptor, producing a pituitary growth hormone pulse and suppressing somatostatin. Mechanically this is the same action as GHRP-2 and hexarelin.

Its appetite effect comes from the same receptor, acting in the hypothalamus. Ghrelin's normal role is to signal hunger before meals, and GHRP-6 reproduces that signal directly and strongly. This is not an off-target effect waiting to be engineered away. It is the receptor doing what it does.

Prolactin and cortisol rise more with GHRP-6 than with GHRP-2, which is the trade for its lower potency at releasing growth hormone. It is the least selective of the three GHRPs on this site.

Separate from the growth hormone axis, GHRP-6 has been studied for direct tissue effects, cardioprotection after ischaemia and wound healing, mediated in part through the CD36 receptor. That work is largely preclinical and is unrelated to why the compound is bought.

Regulatory status — United States

Not approved for human use in any jurisdiction. Studied in humans in early-phase research decades ago; development was not carried through to approval. Sold only as a research chemical.

Last reviewed 16 Aug 2026. Regulatory positions in this category change frequently; we date this line so you can see how current it is.

What it is studied for

Each entry states the evidence behind it. We do not rank indications by effectiveness — for most compounds here, that would be a claim nobody can support.

Raising growth hormone

Clinical trial

The measured pharmacological effect.

EvidenceHuman studies consistently show a growth hormone pulse after dosing. This is the best-established fact about the compound.

Appetite stimulation

Published review

Sometimes the reason for use, more often the reason for stopping.

EvidenceA direct and well-documented consequence of ghrelin receptor agonism. Not developed or approved as an appetite treatment.

Cardioprotection and wound healing

Published review

A genuine research thread, separate from the GH axis.

EvidenceAnimal studies, principally in cardiac ischaemia models. No human trial supports these uses.

Identity and clearance

Molecule

Class
Synthetic hexapeptide, growth hormone secretagogue
Molecular weight
873.01 Da
Length
6 amino acids

Sequence

His-D-Trp-Ala-Trp-D-Phe-Lys-NH2

Pharmacokinetics

Published review
Peak0.3 h
Half-life0.3 h
Substantially cleared2 h
100%50%25%0%half-life 0hdose1h1h2h2h
Modelled from the half-life above, assuming first-order elimination. Illustrative rather than measured — it shows the shape of clearance, not a prediction for any individual.

Cleared faster than GHRP-2. The appetite effect arrives well before the growth hormone pulse peaks.

Dose protocols reported in sources

Displayed for reference only. Every row says where it came from, and a trial protocol and a community convention are not the same kind of information. None of this is fed into the calculator, and none of it is a recommendation.

Dose protocols reported in sources, with the source of each.
GoalDoseFrequencyRouteUnits, 5 mg vialSourceStart this protocol
Growth hormone response, as studied100 mcgSingle dose in study conditionsSubcutaneousRoughly 1 mcg per kilogram, the dose most often used in the human studies that characterised the growth hormone response.10 uClinical trialStart this
Commonly described community protocol100 mcg – 300 mcgOne to three times dailySubcutaneousDescribed in the same pattern as the other GHRPs, usually alongside a GHRH analogue. The hunger is why many people who try this protocol do not continue it.10–30 uCommunity practiceStart this

Start this copies a row into a protocol of your own, which you can then edit. Where a source gave a dose range or an ambiguous frequency, those fields arrive empty — we will not pick a number on your behalf.

CheckRows marked community practice describe what people commonly do, drawn from public discussion. They are not derived from any trial and are not evidence that a dose is safe or effective.

Calculator

Work out what to draw

Pre-filled with a 5 mg vial as a worked example. These are not recommended values — change them to match the vial in front of you.

Dose unit
Your syringe
01020304050607080901004 units0.04 mL

Draw to 4 units on a 1 mL U-100 syringe. That is 0.04 mL, containing 100 mcg of GHRP-6.

Concentration2.5mg / mL
Volume drawn0.04mL
Doses per vial50doses
Per unit25mcg / unit

4 units sits exactly on a printed line.

Bioalmanac performs arithmetic on values you enter. It does not recommend doses, schedules or compounds, and nothing here is medical advice. Confirm every calculation against your vial and syringe before drawing, and speak with a licensed healthcare provider.

Open this calculation in the full calculator

Units, concentration, bacteriostatic water — the glossary defines the vocabulary, and a unit is not a fixed volume.

Safety

Reported effects

  • Intense hungerPublished review

    Very common. The defining effect

    Arrives within about twenty minutes and is strong enough that most people describe it as the main thing the compound does.

  • Rise in prolactin and cortisolClinical trial

    Measured in human studies

    Larger than with GHRP-2. Persistently raised prolactin can affect libido, mood and menstrual cycles.

  • Water retention and puffinessCommunity practice

    Commonly reported

  • Tingling or numbness in the handsCommunity practice

    Occasionally reported

    Consistent with carpal tunnel symptoms from raised growth hormone.

  • Flushing and head rush after injectionCommunity practice

    Commonly reported

    Usually within minutes and short-lived.

  • Reduced insulin sensitivityPublished review

    Expected from raised growth hormone

When to stop

  • Numbness, tingling or persistent pain in the hands or wrists.
  • Swelling that does not settle, particularly in the ankles or face.
  • Rising fasting glucose, or new thirst, frequent urination or blurred vision.
  • Nipple tenderness or discharge, or a change in menstrual cycle.
  • Any allergic response: rash, hives, facial swelling or difficulty breathing. Seek urgent care.
  • Any new lump, unexplained weight loss or unexplained persistent pain.

Interactions and situations that need care

  • Active or previous cancerAvoid

    Growth hormone and IGF-1 are proliferative signals, and there is no evidence supporting deliberate elevation of either in someone with malignancy.

  • Diabetes or impaired glucose toleranceUse caution

    Reduced insulin sensitivity from raised growth hormone, compounded here by an appetite effect strong enough to change what someone eats.

  • Disordered eating, current or pastUse caution

    This compound produces strong, artificial hunger on a schedule you control. For anyone with a history of binge eating or a difficult relationship with appetite, that is a specific and foreseeable harm, not an inconvenience.

  • Competing in a tested sportAvoid

    Growth hormone secretagogues are named explicitly in WADA's S2 category and are prohibited at all times, in and out of competition. Whether a current test detects this particular compound is beside the point — the prohibition is on the substance, not on being caught.

  • Pregnancy and breastfeedingAvoid

    No reproductive or developmental safety data.

SportProhibited by the World Anti-Doping Agency under S2: Peptide Hormones, Growth Factors, Related Substances, at all times, in and out of competition. Growth hormone secretagogues are named explicitly in S2. Prohibition applies whether or not a test can currently detect the specific compound.

What to expect

HonestlyThere is no human efficacy data for this compound, so there is no evidence-based timeline to give. Any site publishing a week-by-week schedule of expected effects has invented it.

  • The hunger is the first thing you will notice, it arrives within about twenty minutes, and it is stronger than people expect.
  • The growth hormone pulse is real and measured. What repeated pulses do to body composition over months has not been studied for this compound.
  • If you are eating in a deficit, this is the wrong peptide in the family. GHRP-2 and ipamorelin do the same job to the growth hormone axis without it.
  • It is the least selective GHRP available. Prolactin and cortisol rise more than with its relatives.
  • The cardiac and wound-healing research is genuine but is almost entirely in animals, and is not what anyone is buying it for.

Storage and handling

Freeze-dried powder
Refrigerated at 2–8 °C, protected from light.
After mixing
Refrigerated at 2–8 °C. Do not freeze once mixed.
Long-term, frozen
Unopened powder is stable at −20 °C or colder.

Printable one-pagerHow to reconstitute a vial, step by step

With other peptides

  • CJC-1295synergistic

    A GHRH analogue and a ghrelin-receptor agonist act through different pathways, so the growth hormone pulse is larger than either produces alone.

  • GHRP-2caution

    Both act on the same receptor. Combining them stacks side effects without stacking the growth hormone response.

  • Hexarelincaution

    The same receptor once more. No mechanistic reason to run two GHRPs together.

  • Ipamorelincaution

    Same receptor, overlapping effects. Ipamorelin exists specifically to avoid GHRP-6's hunger, prolactin and cortisol effects, and combining them gives those back.

Check this against a whole stack

Checking your vial

Research chemicals carry no manufacturing standard, so what the vial looks like is often the only quality signal available before you use it. More on assessing quality and COAs.

  • White cake, clear solution

    Standard for a short hexapeptide.

  • Collapsed, melted or fused cake

    Heat exposure in transit. Refrigerating it afterwards does not undo the damage.

  • Cloudy solution or visible particles after gentle mixing

    Degraded or contaminated. Do not use it.

Questions

How strong is the hunger, really?
Strong enough that it is the most consistent thing people report, and the most common reason they stop. It arrives about twenty minutes after injecting. Treat it as the main effect, not a side effect you might not get.
Why would anyone choose GHRP-6 over GHRP-2?
Almost always because they want the appetite stimulation: someone struggling to eat enough. For raising growth hormone alone, GHRP-2 does it more potently with less prolactin and far less hunger.
Is the cardiac research relevant to me?
Not currently. It is a real body of work, mostly in animal models of cardiac ischaemia, and it does not translate into a reason to take GHRP-6 for heart health. No human trial supports that.

References

  1. Growth hormone response to GHRP-6 in healthy adults

    Journal of Clinical Endocrinology & Metabolism, 1993 · Human pharmacology study

    Healthy adults · About 1 mcg/kg, single dose · Single administration with sampling over hours

    Produced a reproducible growth hormone pulse, with concurrent rises in prolactin and cortisol. Established the pharmacology of the class in humans.

  2. Ghrelin receptor agonists: appetite, growth hormone and the limits of the evidence

    Endocrine review literature, 2018 · Review

    Humans and animals

    Describes appetite stimulation as an intrinsic consequence of ghrelin receptor agonism rather than an avoidable side effect, and notes GHRP-6 as the least selective member of the class.

  3. GHRP-6 in models of cardiac ischaemia and tissue repair

    Preclinical cardiovascular literature, 2015 · Animal studies

    Rodents and larger animal models

    Reported reduced infarct size and improved tissue repair in animal ischaemia models, attributed partly to CD36 signalling rather than to growth hormone. No human trials have tested these findings.

  4. Commonly reported community protocols

    Bioalmanac editorial summary of public community sources, 2026 · Not a study

    Records dose patterns described in public discussion. Carries no evidential weight about safety or effect.

Keep this page honest

If something here is wrong, out of date, or missing a source, tell us and we will fix it and say that we did.

Suggest a correction

This page is educational. It describes what published research reports, not what you should do. Peptides discussed here are largely not approved for human use, and nothing on Bioalmanac is medical advice. No clinician reviews these pages.

Page last updated 16 Aug 2026