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Anti-aging & longevity

Humanin

HN · MT-RNR2 peptide · HNG · S14G-humanin

PreclinicalReviewed 1 Sept 2026

Humanin was found in 2001 by asking an unusual question: in a brain destroyed by Alzheimer's disease, why is a small population of neurons still alive? Screening what those survivors expressed turned up a short peptide that protected other cells from the same insult.

The surprise was where the gene sat. Humanin is encoded inside MT-RNR2, a mitochondrial gene, on the mitochondrion's own chromosome rather than in the nucleus. It was the first of what are now called mitochondrial-derived peptides, and it made the mitochondrion a signalling organ rather than only a power supply.

Circulating humanin falls with age in humans, and is higher in the children of people who live unusually long. That is the observation the longevity interest rests on. It is an association measured in blood, not an effect of giving anybody the peptide.

That distinction is the whole story here. Humanin has a large, genuinely interesting preclinical literature and no completed human intervention trial of any kind. Almost all of the animal work uses HNG, a more potent analogue with a single substitution at position 14, rather than the natural sequence being sold.

How it works

Its best-characterised action is blocking apoptosis. Humanin binds BAX and keeps it from moving to the mitochondrial membrane, which is the committed step in one of the main cell-death pathways.

Outside the cell it signals through at least two receptors: the formylpeptide receptor FPR2, and a trimeric receptor of CNTFR, WSX-1 and gp130 that activates STAT3. Which one matters appears to depend on the tissue.

It also binds IGFBP-3, which is how it intersects with the insulin and IGF-1 axis that most longevity biology runs through. Humanin improves insulin sensitivity in rodents, and this is the likely route.

The mitochondrial origin is not incidental. The peptide appears to be released under stress, which makes it look like a signal from mitochondria to the rest of the body about their own condition — the reason the field calls these retrograde signals.

Vocabulary on this page

Evidence level
The category of human evidence behind a compound, from preclinical through to approved. Stated on every profile here as a category, not an adjective.
Injection site
Where on the body an injection is given. Rotating between sites is standard practice for anything given repeatedly.
Peptide
A short chain of amino acids: the same building blocks as a protein, in a chain short enough to behave differently.
Protocol
One compound, with a dose, a frequency and a length: the plan, as opposed to what was actually taken.

The whole glossary →

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.

Neuroprotection

Published review

The question it was discovered by.

EvidenceProtects neurons from amyloid-beta toxicity in cell culture and in rodent models. No human trial has tested it for any neurological condition.

Metabolic and insulin sensitivity

Published review

Where the mechanism is clearest.

EvidenceImproves insulin sensitivity in rodents, plausibly through IGFBP-3 binding. Human data is limited to observational measurement of the body's own humanin levels.

Longevity

Published review

An association, and only that.

EvidenceCirculating humanin declines with age and is higher in the offspring of long-lived people. Nobody has given humanin to a person and measured anything.

Regulatory status — United States

Not approved anywhere, for any indication, and never taken into a human trial. Sold as a research chemical. Material on the market is not a clinical product and has no manufacturing standard behind it.

Last reviewed 1 Sept 2026. Regulatory positions in this category change frequently; we date this line so you can see how current it is.

Identity and clearance

Molecule

Class
Mitochondrial-derived peptide
Molecular weight
2687.3 Da
Length
24 amino acids

Sequence

MAPRGFSCLLLLTSEIDLPVKRRA

Encoded within MT-RNR2 on mitochondrial DNA rather than in the nuclear genome. The analogue used in most animal work, HNG, substitutes glycine for serine at position 14 and is substantially more potent.

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
Commonly described community protocol1 mg – 5 mgDailySubcutaneousScaled from rodent studies by guesswork, and most of those studies used HNG rather than humanin. There is no human dose because there has been no human study.20–100 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.

Safety

Reported effects

  • Unknown, in fullCommunity practice

    Unknown

    No human has taken humanin in a study. There is no adverse-event profile because nobody has ever collected one.

  • Consequences of suppressing apoptosisPublished review

    Unknown, and the specific concern

    Its central action is blocking a cell-death pathway. Apoptosis is also how the body removes damaged and precancerous cells, and no study has looked at what sustained pharmacological suppression does over time.

When to stop

  • Any new lump, or a persistent unexplained symptom.
  • Unexplained weight loss, night sweats or persistent fatigue.
  • Injection site reaction that spreads or does not settle.
  • Any allergic response: rash, hives, facial swelling or difficulty breathing. Seek urgent care.

Interactions and situations that need care

  • Any history of cancerAvoid

    Humanin's defining action is inhibiting apoptosis, which is one of the mechanisms that clears damaged cells. Deliberately suppressing it is the clearest specific risk the molecule carries.

  • Pregnancy and breastfeedingAvoid

    No reproductive or developmental data of any kind.

  • Using it at all, at this stageUse caution

    A compound with no human exposure in any controlled setting. The preclinical literature is real and interesting, and it is not a safety record.

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.

  • No human intervention trial has ever been completed, for any indication.
  • The longevity claim rests on measuring the body's own humanin, not on giving anybody more of it.
  • Most of the animal work uses HNG, a different and more potent molecule than the one sold as humanin.
  • Its main mechanism is blocking apoptosis, which is a reason for caution as much as a reason for interest.
  • It is a genuine discovery — the first mitochondrial-derived peptide — and that is a separate matter from whether injecting it does anything for you.

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

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.

  • No certificate of analysis

    For a peptide with no clinical reference product, third-party identity and purity testing is the only evidence the vial holds what the label says.

  • Humanin or HNG

    These are different molecules and vendors are not consistent about which they sell. The analogue is more potent, and a label saying only “humanin” does not settle it.

Questions

Is humanin actually made by the human body?
Yes. It is encoded in mitochondrial DNA and circulates in blood, and levels fall with age. That is why it is interesting. It is not why injecting it would work — plenty of things the body makes do nothing useful when given from outside.
What is HNG?
An analogue with glycine substituted for serine at position 14, considerably more potent than the natural peptide. Most of the animal literature people cite for humanin was actually done with HNG, which is worth knowing when reading claims about either.

References

  1. The molecular structure and role of humanin in neural and skeletal diseases, and in tissue regeneration

    Frontiers in Cell and Developmental Biology, 2022 · Narrative review

    Cell culture and animal models

    Summarises humanin's cytoprotective actions — BAX inhibition, FPR2 and CNTFR/WSX-1/gp130 signalling, IGFBP-3 binding — across neural, skeletal and regenerative contexts. The evidence base is preclinical throughout; no completed human intervention trial is described.

  2. Naturally occurring mitochondrial-derived peptides are age-dependent regulators of apoptosis, insulin sensitivity and inflammatory markers

    Aging, 2016 · Observational, with animal work

    Human plasma samples across age ranges, plus rodent models

    Circulating humanin declines with age in humans and is higher in the offspring of long-lived individuals. Rodent work supports effects on insulin sensitivity. The human component measures endogenous levels; it does not administer the peptide.

  3. Clinic and community practice, unverified

    Research-chemical vendor listings and forums, 2026 · Not a study

    Not applicable

    Doses circulating in community sources have no published basis. They are reproduced here because people are using them, not because anything supports them.

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 1 Sept 2026