Epithalon
Grade CRussian preclinical and small-cohort human studies reported lifespan and biomarker improvements. Independent replication is limited.
Russian preclinical and small-cohort human studies reported lifespan and biomarker improvements. Independent replication is limited.
Read the list below as hypotheses, not benefits. This compound is graded C: the effects described come from animal studies, cell work or anecdote — reliable human trials are absent.
Tetrapeptide (Ala-Glu-Asp-Gly) hypothesized to upregulate telomerase activity and normalize pineal melatonin secretion.
Educational reference only — not medical advice.
Epithalon is administered subcutaneous, intranasal with an approximate systemic half-life of Short, hours. Steady-state and tissue-level effects can outlast plasma concentration, which is why dosing frequency (Daily) is designed to match receptor kinetics rather than plasma exposure. Tetrapeptide (Ala-Glu-Asp-Gly) hypothesized to upregulate telomerase activity and normalize pineal melatonin secretion.
Sterile technique is not optional. Use a fresh needle for every injection.
Download a printable version of this checklist to log baseline, weekly and post-cycle results.
Grade C — mechanistic hypothesis and animal or in-vitro data only. No controlled human trials. Treat as experimental; risks are not fully known.
Below are the primary references used to grade Epithalon. Follow the links for full-text where available and cross-check against the current literature.
5–10 mg, Daily, for 10–20 day cycles, 2× per year. Route: Subcutaneous, intranasal. Timing: Evening. Half-life: Short, hours.
Tetrapeptide (Ala-Glu-Asp-Gly) hypothesized to upregulate telomerase activity and normalize pineal melatonin secretion.
Most users track a full 10–20 day cycles, 2× per year cycle before judging response. Subjective changes can appear within 1–3 weeks, but objective biomarker shifts typically need the full cycle plus repeat labs.
Research chemical; not approved for human use.
Largely unknown long-term; Injection site reactions.
Commonly combined with: Magnesium glycinate, Glycine. Introduce one compound at a time to preserve attribution.
Baseline and post-cycle: full blood count, comprehensive metabolic panel, and category-specific markers for longevity peptides (see the monitoring section on this page).
Off-cycle periods let receptor sensitivity and endogenous feedback normalise. Continuous dosing without a wash-out typically produces diminishing returns and a poorer safety margin.
Further reading: Research library → · Protocols →
| Attribute | EpithalonThis page | Thymosin Alpha-1 | Tesamorelin |
|---|---|---|---|
| Evidence | Grade C | Grade B | Grade A |
| Category | Longevity | Longevity | Growth Hormone |
| Best for | Telomerase activation (research) | Immune modulation | Visceral fat, growth hormone axis |
| Typical dose | 5–10 mg | 1.6 mg | 2 mg (1.28 mg for the newer F8/WR formulation) |
| Frequency | Daily | Twice weekly | Once daily |
| Route | Subcutaneous, intranasal | Subcutaneous injection | Subcutaneous injection |
| Legal status | Research chemical; not approved for human use. | Approved as Zadaxin in over 35 countries for chronic hepatitis B; not FDA-approved in the United States, where the FDA has moved thymosin alpha-1 to the category of substances that cannot be compounded. Research-grade material is unverified for purity or identity. | FDA-approved as Egrifta and Egrifta SV/WR for HIV-associated lipodystrophy only, and prescription-only. Use for body composition or anti-ageing is off-label. Material sold online as research-grade tesamorelin is not the approved product and carries no purity guarantee. |
| Action | Current page | View → | View → |