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EmergingResearch compound

SR9009 (Stenabolic)

A research chemical advertised as a REV-ERB agonist, from the Burris lab at Scripps. Real metabolic effects in mice (Solt 2012, Nature) but ZERO clinical trials in humans. PNAS 2019 showed the effects do not run through REV-ERB, which undercuts the entire marketing story.

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SR9009 (Stenabolic) vial

WHAT IS SR9009 (STENABOLIC)?

Detailed overview

SR9009 (Stenabolic) is a synthetic compound described by Thomas Burris's laboratory at Scripps Research as an agonist of the REV-ERB nuclear receptor. Its reputation comes from the 2012 Nature paper by Solt and colleagues: in mice the compound raised metabolic rate, reduced fat mass and altered circadian behaviour. That is where the "exercise in a bottle" slogan comes from. Two things are missing from this story, and both are decisive. First, the mechanism does not hold. The 2019 PNAS paper by Dierickx and colleagues showed that SR9009 affects proliferation and metabolism even in cells genetically lacking both REV-ERB-alpha and REV-ERB-beta. If the effect appears without REV-ERB, then REV-ERB is not mediating it. The mechanism advertised in shops is therefore incomplete at best and wrong at worst, and the compound's real targets are unknown. Second, there is no human data. SR9009 has never been tested in a clinical trial. This is not a case of sparse data: it is zero. On top of that, rodent pharmacokinetics indicate very poor oral bioavailability and a short half-life, so most of an oral dose never reaches the circulation. In practice this means a user knows neither how much drug was absorbed nor what the absorbed fraction is doing. It is on this site because it is sold and searched for. The scientific claims used to sell it, however, do not stand up.

Advertised mechanism

REV-ERB-alpha/beta agonist, regulator of the circadian clock and energy metabolism.

Status of that mechanism

REFUTED: PNAS 2019 found the effect persists in cells lacking REV-ERB.

Human trials

None. Not a single clinical study has been performed in humans.

Oral bioavailability

Very poor in rodents with a short half-life; the efficacy of oral dosing is doubtful.

Legal status

Not a medicine. WADA-banned (S4.5, metabolic modulators).

Data console

Lab data

/lab/molecular-data.jsonLIVE
> Androgenic:AnabolicNot applicable: not an androgen, does not bind the androgen receptor.
> AR bindingDescribed as a REV-ERB-alpha/beta agonist, but the 2019 PNA…
> Active half-lifeismeretlen humánban
> Detection windowWADA-accredited laboratories detect it in urine by mass spectrometry. Banned year-round in competitive sport.
> AromatizationNO. SR9009 is not a steroid and is not a substrate of aromatase.
> HepatotoxicityUNKNOWN. It is not 17-alpha-alkylated, so the classic oral-steroid liver injury mechanism does not apply, but there is no human hepatic safety data at all. "Unknown" here is not the same as "low".

Safety

Side effects, stop signs, contraindications

Side effects · 4

  • Unknown human safety profile: no clinical trial has ever been run in humans, so the adverse-effect list is not incomplete but NON-EXISTENT. That fact is itself the most important risk datum.
  • Circadian disruption: REV-ERB is a core regulator of the internal clock, and in animals the compound altered sleep-wake patterns and locomotor activity.
  • Off-target activity: PNAS 2019 showed the compound affects proliferation and metabolism in cells lacking REV-ERB, so it acts on unidentified additional targets.
  • Unpredictable dosing: poor oral absorption and a short half-life make the actually absorbed amount impossible to estimate, which undermines any dose recommendation.

Contraindications · 4

  • Any human use: there is no clinical data supporting any dosing whatsoever. This is not caution but the factual consequence of missing data.
  • Pregnancy, breastfeeding, childhood: complete absence of data.
  • Competitive sport under testing: WADA bans metabolic modulators (S4.5).
  • Sleep disorder or shift work: interfering with a core circadian regulator is especially unpredictable here.

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Studies

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MolekulaX Editorial Team·Source-verified · PubMed · FDA · EMA

The information here is for educational and scientific purposes only. Performance-enhancing compounds (AAS, prohormones, stimulants, doping agents) are illegal without prescription in Hungary and most of the EU, and carry serious health and legal risks. WADA bans them in competitive sport. This is NOT a usage guide, and we do not encourage any illegal use. If you do use them, medical supervision and regular bloodwork are ESSENTIAL. Severe endocrine, cardiovascular, hepatic and psychiatric side effects are possible.