No. 036 · Longevity & Immune · Longevity Peptide
Epithalon
Also known as: EpitalonEpithaloneAEDG
- Not FDA approved
- WADA ✗ S0
2D structure from PubChem CID 219042 (Epitalon), matched by molecular formula. Hydrogens on carbon are implied.
- Nonpolar 2
- Negative charge 2
Each dot is a residue placed around the ring from N- to C-terminus; its distance from the centre reflects its chemistry.
Quick answers
- What is Epithalon?
- A synthetic tetrapeptide (Ala-Glu-Asp-Gly) developed by Khavinson, modeled on the pineal extract epithalamin.
- How strong is the evidence for Epithalon?
- Tier B (small human studies) on the peptidemeta evidence scale. Human data are limited to small biomarker studies and an older controlled study in retinitis pigmentosa, almost all from one research group; no randomized trial exists. Most evidence is cell and animal work.
- Is Epithalon FDA-approved?
- No. Epithalon is not approved by the FDA for any use.
- Is Epithalon banned in sport?
- Yes. Epithalon is prohibited in sport by the World Anti-Doping Agency under S0 (non-approved substances).
- How does Epithalon work?
- In cultured human fibroblasts, Epithalon (Ala-Glu-Asp-Gly) was reported to induce expression of the telomerase catalytic subunit (hTERT), telomerase activity and telomere elongation. It is also proposed to stimulate pineal melatonin production and restore circadian neuroendocrine function.
- What is known about the safety of Epithalon?
- Human safety data are limited to small studies from the Khavinson group; no long-term controlled safety data exist. Theoretical concern that telomerase activation could promote cancer has not been ruled out.
Last reviewed · editorial policy · markdown
Evidence
- D In vitro
- C Animal
- B Human pilot
- A RCT
- S Approved
TIER B — Human data limited to small, open-label or pharmacokinetic studies.
Human data are limited to small biomarker studies and an older controlled study in retinitis pigmentosa, almost all from one research group; no randomized trial exists. Most evidence is cell and animal work.
Tiers rate the strength of published evidence — not effectiveness, safety, or a recommendation.
At a glance
- Residues
- 4 amino acids, N→C
- Molecular weight
- 390.4 Da
- Formula
- C14H22N4O9
- Routes studied
- Subcutaneous, Intramuscular Routes used in published research
- FDA
- Not approved
- WADA
- Prohibited · S0 Non-approved substances
Sequence
Note Synthetic tetrapeptide based on the amino-acid composition of epithalamin, a pineal gland extract.
Overview
A synthetic tetrapeptide (Ala-Glu-Asp-Gly) developed by Khavinson, modeled on the pineal extract epithalamin. In cultured human cells it has been reported to activate telomerase and lengthen telomeres; human evidence is limited to small studies.
Research status Telomerase findings come from cell culture; human data limited to small studies from one group (e.g. a 2002 controlled study in retinitis pigmentosa); no randomized trials
Mechanism
In cultured human fibroblasts, Epithalon (Ala-Glu-Asp-Gly) was reported to induce expression of the telomerase catalytic subunit (hTERT), telomerase activity and telomere elongation. It is also proposed to stimulate pineal melatonin production and restore circadian neuroendocrine function. Whether these effects occur in humans has not been established.
Effects reported in research
Reported outcomes, not promises. Human data are limited to small studies, and many of these findings are preclinical.
- Telomerase activation and telomere elongation (cell culture)
- Improved circadian melatonin secretion
- Antioxidant protection at the cellular level
- Enhanced immune surveillance markers
Safety & unknowns
Human safety data are limited to small studies from the Khavinson group; no long-term controlled safety data exist. Theoretical concern that telomerase activation could promote cancer has not been ruled out. Not FDA-approved. Little independent Western clinical data.
Unknowns. No randomized controlled trials have been published. Small studies cannot detect uncommon or long-term harms.
Informational only — not medical advice. peptidemeta publishes no dosing, protocols, or sourcing. Talk to a qualified clinician about any treatment decision.
Studies [4]
- Review 2026
Epitalon and Epithalamin: A Narrative Review of Mechanistic, Preclinical, and Clinical Evidence
Concludes that human evidence for epitalon is limited to small physiological or biomarker studies and an older controlled study, with no adequately powered randomized trial.
- Preclinical 2004
Peptide promotes overcoming of the division limit in human somatic cell
In cultured human fetal lung fibroblasts, Epithalon lengthened telomeres and the treated cells divided about 10 more times than controls.
- Preclinical 2003
Epithalon peptide induces telomerase activity and telomere elongation in human somatic cells
Adding Epithalon to telomerase-negative human fetal fibroblast cultures induced telomerase catalytic-subunit expression, enzyme activity, and telomere elongation.
- Clinical trial 2002
Pineal-regulating tetrapeptide epitalon improves eye retina condition in retinitis pigmentosa
Reported retinal functional improvements in rats with hereditary retinal degeneration and a positive clinical effect in most treated patients with retinitis pigmentosa in a small controlled study.
Status sources
Sources behind the tier, regulatory status, sequence and dates on this page.
- Epitalon and Epithalamin: narrative review of the evidence (Int J Mol Sci 2026) pubmed.ncbi.nlm.nih.gov
- Khavinson et al. 2002 — epitalon in retinitis pigmentosa (controlled clinical trial) pubmed.ncbi.nlm.nih.gov
- PubChem CID 219042 (epitalon) pubchem.ncbi.nlm.nih.gov
- WADA 2026 Prohibited List — S0 non-approved substances wada-ama.org
Cite this entry
peptidemeta. (2026). Epithalon. In peptidemeta: The peptide library, ranked by evidence. Retrieved November 8, 2026, from https://peptidemeta.com/p/epithalon/
@misc{peptidemeta-epithalon,
title = {Epithalon},
author = {{peptidemeta}},
year = {2026},
howpublished = {\url{https://peptidemeta.com/p/epithalon/}},
note = {Accessed 2026-11-08}
} Accessed date reflects when you opened this page. Cite primary studies for scientific claims.