Roidipedia.Compound reference & reporting
06 AUG 2026
CompoundsAnabolic steroid Androstanazole
Anabolic steroidAndrogenOralDihydrotestosterone derivativePyrazole-fused

Androstanazole

Also known as Pyrazole-fused androstane analogue

Androstanazole is a pyrazole-fused dihydrotestosterone derivative belonging to the same heterocyclic-steroid family as stanozolol, described in older medicinal-chemistry literature as an orally active anabolic candidate. Human data are essentially absent and it is of historical/chemical interest.

01 Overview

Androstanazole is one of several A-ring pyrazole-fused androstane steroids explored during the mid-20th-century search for orally active anabolics, the most successful of which was stanozolol. The fused pyrazole ring confers oral activity and non-aromatisable behaviour.

Unlike stanozolol, androstanazole never reached significant clinical or commercial use, and the compound survives mainly in structure-activity surveys. Its expected profile is inferred from the pyrazole-androstane class rather than from dedicated human study.

02 Mechanism

Androgen-receptor agonist; an A-ring pyrazole-fused 5-alpha-androstane derivative giving oral bioavailability and resistance to aromatisation.

03 Dosing

TierDoseRouteNotes
Historical (inferred)5–20 mg/dayOralInferred from stanozolol-class dosing; no established human range.

Ester comparison

EsterHalf-lifeInjection freq.Testosterone by mass

04 Effects

EffectMagnitudeEvidence
Anabolic activityAnabolic action inferred from pyrazole-androstane structure; unconfirmed in humans.unquantifiedPreclinical
Low estrogenic activityDoes not aromatise, so estrogenic effects are minimal.non-aromatisingPreclinical

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
HepatotoxicityHepatic strain anticipated for an oral heterocyclic androgen.ModerateClass effectPreclinical
HPTA suppressionSuppression of endogenous testosterone.ModerateExpectedPreclinical

07 References

Heterocyclic-fused androstane anabolic steroids: structure-activityJournal of Medicinal Chemistry (review)

08 Discussion0 comments

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