PeptideTrace
Research CompoundBovine Pineal Extract (Russian Approval)

Epithalamin

Epithalamin extract

C

Evidence Grade C — Moderate human evidence. 70 published studies, 29 human. 0 registered clinical trials.

70 studiesUSEUCA

Overview

Epithalamin is a crude extract from bovine (cow) pineal glands — the parent substance from which the synthetic peptide Epitalon was derived. Unlike Epitalon, it is an undefined biological mixture rather than a single molecule. It has been used clinically in Russia but has not been evaluated through Western regulatory processes.

Research Activity

70studies
Human 29
Animal 41
In-vitro 6
Reviews 12

70 published studies: 29 human, 41 animal, 6 in-vitro, 12 reviews

Regulatory Status

US
Not approved by FDA(FDA)
EU
Not authorised by EMA(EMA)
CA
Not approved by Health Canada(Health Canada)

Legal Status

USNot applicable (not approved)
EUNot applicable (not authorised)
CANot applicable (not approved)

Summary

Epithalamin is approved in Russia. It has not been approved by the FDA, EMA, or other major Western regulatory agencies. A study of elderly subjects reported reduced mortality with combined Epithalamin and Thymalin treatment over long-term follow-up. These results come from the Khavinson research programme and have not undergone Western regulatory review.

As an undefined biological extract from bovine pineal tissue, Epithalamin faces the same molecular characterisation and quality standardisation challenges as Thymalin (#121). See also Epitalon (#117) for the synthetic active component.

Mechanism of Action

Research proposes that Epithalamin's active component is the tetrapeptide Epitalon (AEDG), with a proposed mechanism involving telomerase activation through hTERT gene expression. As an undefined extract, the specific active components and their mechanisms cannot be precisely characterised. See Epitalon (#117) for the proposed mechanism of the isolated active component.

Research Summary

Research from the Khavinson group reports reduced mortality with combined Epithalamin and Thymalin treatment in elderly subjects over long-term follow-up. However, every preclinical and clinical study through 2025 was conducted by the same research group, with no independent confirmation. As an undefined crude bovine extract, Epithalamin faces molecular characterisation and quality standardisation challenges that are more severe than for defined synthetic peptides. A theoretical prion contamination risk exists for animal-derived brain tissue products. No formal pharmacokinetic data or safety trials meeting international standards have been conducted. Approximately half of the published studies are in Russian only.

Clinical Trials

No trials registered on ClinicalTrials.gov for this compound.

The information on this page is provided for educational and research reference purposes only. This is not medical advice. Always consult a qualified healthcare professional before making any health-related decisions.

Related Compounds

GHK-Cu

Research Compound
Copper Tripeptide (Cosmetic/Research)

GHK-Cu has no pharmaceutical authorisation from any regulatory agency. It is widely available as a cosmetic ingredient in over-the-counter skincare products, where it is marketed for skin conditioning. A small study comparing GHK-Cu cream to vitamin C and retinoic acid creams reported improvements in skin appearance measures. No pharmaceutical clinical trials for injectable GHK-Cu have been completed. The compound's cosmetic use (topical, in formulated skincare products) should be clearly distinguished from its unregulated availability as an injectable research compound. These represent fundamentally different risk profiles.

Epitalon

Research Compound
Khavinson Bioregulator Tetrapeptide (Unregulated)

Epitalon has no marketing authorisation from any major regulatory agency. No controlled human clinical trials have been conducted. Animal lifespan studies in mice reported by the Khavinson group form the core evidence base. The telomerase activation claims are based on in vitro studies and mouse models from a single research programme. Independent replication of the key findings has not been published. The relationship between in vitro telomerase activation and any clinical outcome in humans is not established. Products available through unregulated channels lack pharmaceutical quality assurance.

FOXO4-DRI

Research Compound
Senolytic Peptide (Preclinical)

FOXO4-DRI has no marketing authorisation. No human clinical trials have been conducted. The evidence comes from a single high-profile publication (Cell, 2017) demonstrating effects in three mouse models. The senolytic field is an active area of pharmaceutical research, but FOXO4-DRI faces significant challenges for clinical translation, including its large size (46 amino acids), manufacturing complexity, and the absence of human pharmacokinetic or safety data. Products available through unregulated channels — which would need to reliably synthesise a 46-amino-acid all-D-amino-acid peptide — face exceptional quality assurance challenges.