COMPOUNDS / STEROID / EPISTANE
STEROID

EPISTANE

HIGH RISK
BEST FOR:Lean Mass●●●●○○○○○○4/10
EPISTANE · HEMAPOLIN · 17Α-METHYLEPITHIOSTANOL · METHYLEPITHIOSTANOL · METHYL-EPI · EPI · 2Α,3Α-EPITHIO-17Α-METHYL-5Α-ANDROSTAN-17Β-OL · METHYLATED EPITIOSTANOL · EPISTANE
Anabolic SteroidDesigner Steroid17α-AlkylatedHepatotoxicBodybuildingWADA Banned

Oral 17α-alkylated designer anabolic steroid with epithio ring modification, known for hepatotoxicity risk

ROUTE / DOSAGE
LOW10mg
STANDARD20-30mg
HIGH40mg+
Note: 17α-alkylated - hepatotoxic; limit cycle length to 4-6 weeks max
CYCLE
4-6 weeks max 6 weeks off-cycle equal or longer
BIOAVAILABILITY
~50% oral higher sublingual
ACTIVE DURATION
8-12h (subjective)
STORAGE
Room temperature dry away from light keep in original sealed container
HALF-LIFE
6-8h (plasma)
DURATION BREAKDOWN
Total8-12h
Onset1-2h
Come up2-4h
Peak4-8h
Offset4-8h
After effectsdays
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
6 documented
Increased lean muscle mass
Increased strength
Dry non-aromatizing gains
Enhanced recovery
Anti-estrogenic activity
Increased training drive
§ 02 — RISKS
Severe hepatotoxicity and cholestasis with 14-61x bile acid elevation documented in clinical cases
Significant testosterone suppression requiring PCT
Adverse lipid changes (reduced HDL, elevated LDL)
Androgenic effects including hair loss, acne, prostate enlargement
Cardiovascular strain including hypertension
Product contamination with desoxymethyltestosterone and other unlisted steroids
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Epistane is a designer anabolic steroid that appeared in dietary supplements sold online, often marketed as prohormones. In vitro studies using human hepatocytes demonstrate that even low concentrations (0.01 μM) upregulate bile acid synthesis genes and transporters, providing a molecular basis for the cholestasis observed clinically. Four documented cases of long-lasting cholestasis following epistane consumption showed 14- to 61-fold increases in serum bile acid pools, primarily conjugated cholic acid. Analytical studies confirmed that commercial epistane products contain not only the labeled compound but also desoxymethyltestosterone (madol) and isomeric impurities, raising additional safety concerns. No controlled human trials exist; all evidence comes from case reports, in vitro studies, and anti-doping analytical chemistry. The large phenotypic variability in bile acid synthesis enzymes may explain the idiosyncratic nature of epistane-induced liver injury.

§ 06 — SOURCES
[1]
Epistane causes cholestasis by upregulating bile acid synthesis in human hepatocytes
pubmed.ncbi.nlm.nih.gov ↗
[2]
Analysis of 17alpha-methylepithiostanol and desoxymethyltestosterone in dietary supplements
pubmed.ncbi.nlm.nih.gov ↗
[3]
In vivo metabolism of the designer anabolic steroid hemapolin in the thoroughbred horse
pubmed.ncbi.nlm.nih.gov ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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