Roidipedia.Compound reference & reporting
06 AUG 2026
CompoundsAnabolic steroid Thiomesterone
Anabolic steroidAndrogenTestosterone derivativeOral17-alpha-alkylated

Thiomesterone

Also known as Tiomesterone · Emdabol · Emdabolin

Thiomesterone (tiomesterone) is an orally active anabolic-androgenic steroid, a 1,7-bis(acetylthio) derivative of methyltestosterone, marketed historically in Europe as Emdabol. It behaves as a 17-alpha-methylated oral androgen with the two acetylthio groups distinguishing it from the parent compound.

01 Overview

Thiomesterone was introduced in the 1960s as an oral anabolic agent and appeared in several European markets under the brand Emdabol. It is essentially methyltestosterone bearing acetylthio substitutions at the 1-alpha and 7-alpha positions, which modestly alter its pharmacology.

As a 17-alpha-alkylated oral steroid it carries the hepatic and endocrine liabilities typical of the class. It has been little studied in modern controlled trials, and most information derives from older pharmacological references and its historical clinical use for debilitated states.

02 Mechanism

Androgen-receptor agonist; a 17-alpha-methyl, 1,7-bis(acetylthio) methyltestosterone derivative with oral bioavailability.

03 Dosing

TierDoseRouteNotes
Historical5–20 mg/dayOralApproximate range from older European formularies; poorly documented.

Ester comparison

EsterHalf-lifeInjection freq.Testosterone by mass

04 Effects

EffectMagnitudeEvidence
Anabolic / weight gainUsed historically to promote weight gain and recovery in debilitated patients.unquantifiedAnecdotal
Androgenic supportAndrogen-receptor agonism inferred from methyltestosterone lineage.unquantifiedPreclinical

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
HPTA suppressionSuppression of endogenous testosterone.ModerateExpectedPreclinical
HepatotoxicityCholestasis and transaminase elevation characteristic of 17-alkylated orals.SevereClass effectClinical

07 References

Anabolic steroids: pharmacology of oral 17-alkylated agentsJournal of Steroid Biochemistry (review)

08 Discussion0 comments

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This page is reference information, not medical advice. Doses and protocols are documented as they appear in the clinical literature and in practice — describing them is not a recommendation to use them. Countermeasures listed here are not a substitute for a physician. Legal status varies by jurisdiction and changes.