Skip to content
BiologicalX

Comparison

DHEA vs Epitalon

Side-by-side of DHEA and Epitalon. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

DHEA

  • Adrenal androgen precursor; serum DHEA-S declines progressively after the third decade of life
  • OTC dietary supplement in US under DSHEA 1994; prescription in EU, UK, Canada, Australia
  • FDA approved as Intrarosa (6.5 mg vaginal insert) for postmenopausal dyspareunia in 2016
  • Acts as tissue-specific prohormone converted intracrinologically to testosterone and estrogens
  • Best evidence: adrenal insufficiency replacement and vaginal atrophy; weaker on cognition and longevity
  • WADA banned in competitive sport; banned in NCAA, MLB, NFL, IOC settings

Epitalon

  • Synthetic tetrapeptide (Ala-Glu-Asp-Gly) developed at the St. Petersburg Institute of Bioregulation
  • Russian clinical literature reports mortality reduction in elderly cohorts and improved melatonin output
  • Reported telomerase activation in human somatic cell culture and lifespan extension in mice and Drosophila
  • Independent Western replication is essentially absent; no FDA-standard RCTs
  • Anecdotal protocols use 5 to 10 mg subcutaneously daily for 10 to 20 day cycles, 2 to 4 times yearly
  • Not currently on the WADA Prohibited List

Side-by-side

Attribute DHEA Epitalon
Category hormone peptide
Also known as dehydroepiandrosterone, prasterone, Intrarosa Epithalon, Ala-Glu-Asp-Gly, AEDG, Epithalamin (precursor extract)
Half-life (hr) 12 0.5
Typical dose (mg) 25 5
Dosing frequency daily, typically morning daily during cycle
Routes oral, vaginal, topical subcutaneous, intramuscular, intranasal
Onset (hr) 1 24
Peak (hr) 1 168
Molecular weight 288.42 390.35
Molecular formula C19H28O2 C14H22N4O9
Mechanism Steroid prohormone converted intracrinologically to testosterone and estrogens in target tissues; also exerts direct effects via sigma-1 receptor, GABA-A modulation, and glucocorticoid receptor interaction. Synthetic tetrapeptide proposed to interact directly with DNA and chromatin to modulate tissue-specific gene expression. Reported effects include telomerase activation, increased melatonin output from pineal cells, and circadian normalization.
Legal status OTC supplement in US (DSHEA 1994); prescription in EU, UK, Canada, Australia Not FDA approved; registered in Russia under domestic pharmaceutical framework; research-use-only grey market in US/EU
WADA status banned unknown
DEA / Rx OTC supplement in US (not scheduled); Rx in EU, UK, Canada, Australia Not scheduled (research chemical)
Pregnancy Contraindicated in pregnancy Insufficient data; not recommended
CAS 53-43-0 307297-39-8
PubChem CID 5881 219042
Wikidata Q411733 Q5384126

Safety profile

DHEA

Common side effects

  • acne
  • oily skin
  • hirsutism (women)
  • gynecomastia (men, higher doses)
  • irritability
  • insomnia

Contraindications

  • hormone-sensitive cancer (breast, ovarian, prostate)
  • active liver disease
  • uncontrolled lipid disorder
  • pregnancy and lactation

Interactions

  • warfarin: case reports of altered INR; monitor(moderate)
  • estrogens (HRT): additive estrogenic effect via conversion; monitor(moderate)
  • insulin: may improve insulin sensitivity slightly; monitor glucose(minor)
  • anastrozole: may reduce DHEA-derived estrogen; clinical relevance unclear(minor)

Epitalon

Common side effects

  • injection-site reactions
  • occasional mild headache (rare)

Contraindications

  • pregnancy
  • lactation
  • active malignancy (theoretical telomerase concern)
  • concurrent immunosuppression

Interactions

  • melatonin: potential additive effect on circadian and pineal output; no controlled data(minor)

Which Should You Take?

DHEA comes out ahead for most readers on the criteria we weight: 2 catalogued goals, OTC dietary supplement, oral dosing, with a Tier-A outcome catalogued. Epitalon is the right call when one of the conditionals below applies.

  • If your priority is hormonal optimization, pick DHEA.
  • If your priority is sleep onset or sleep quality, pick Epitalon.
  • If your priority is circadian regulation, pick Epitalon.

Edge case: If you want to avoid research-only / gray-market sourcing, DHEA is the more accessible choice.

Default choice: DHEA. Lower friction to source, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for Epitalon only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between DHEA and Epitalon?

DHEA and Epitalon differ in category (hormone vs peptide), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, DHEA or Epitalon?

DHEA half-life is 12 hours; Epitalon half-life is 0.5 hours.

Can you stack DHEA with Epitalon?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

Go deeper