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Stenabolic

Also known as: SR9009, SR-9009

5
1 · Natty510 · Enhanced

Lower numbers = closer to natural. Higher numbers = more enhanced.

Why this rating?

Stenabolic (SR9009) is a Rev-Erb agonist that affects circadian rhythm and metabolism. Rodent studies (Woldt et al., 2013, Nature Medicine) show increased mitochondrial activity and exercise capacity (longer treadmill running time/distance in mice), while a separate rodent study (Solt et al., 2012, Nature) showed circadian and metabolic effects, but there are no published controlled human trials, so real-world effectiveness in a training human is mechanistically plausible but unconfirmed. It does not affect hormones (no testosterone suppression, no PCT needed) and has zero direct anabolic/muscle-building effect. It is explicitly WADA-prohibited as a metabolic modulator (Rev-erbα agonist, S4.4.1). Oral bioavailability is reportedly very poor (community estimates around 1-2%, not from a formal human PK study). Rated 5 as it offers a plausible metabolic/endurance enhancement beyond natural levels but without hormonal manipulation or confirmed human efficacy data, similar to Cardarine in mechanism, but backed by thinner evidence.

Overview

A Rev-Erb agonist that improves metabolic rate and circadian rhythms. Enhances exercise capacity and metabolism without affecting hormones.

Purpose & Use Cases

Metabolic Enhancement

Increases metabolic rate and energy expenditure.

Exercise Capacity

Improves endurance and exercise performance.

Circadian Regulation

May improve sleep-wake cycles and circadian rhythm.

Benefits

  • Increased metabolism
  • Enhanced exercise capacity
  • No hormonal effects
  • May improve sleep patterns
  • Fat loss support

Good to Know

A Rev-ErbA agonist, not a SARM or a stimulant

SR9009 works on the circadian clock protein Rev-ErbA, ramping up mitochondrial biogenesis and fat/glucose oxidation. It has no androgenic activity, no aromatization, no HPTA suppression and no PCT requirement. It is mechanistically different from Cardarine (PPAR-delta) even though the two are marketed together as "cardio" compounds.

The human evidence is very thin, mostly mice

The headline findings: circadian/metabolic effects (Solt et al., 2012, Nature) and exercise capacity/mitochondrial biogenesis (Woldt et al., 2013, Nature Medicine), all come from mice, largely via injection. There are essentially no controlled human trials, so its real-world effect in a lifting, dieting human is mechanistically plausible but unproven. This is a place where community hype clearly outruns the data.

Oral bioavailability is poor and the half-life is short

Community/vendor estimates put oral SR9009 bioavailability in the low single-digit percent range with a ~4 hour half-life, so a large fraction of an oral dose is functionally inactive, but no formal human pharmacokinetic study has ever been published to confirm either figure. This is why users split it into 3-4 daily doses or use injectable/sublingual forms, and why claimed oral results should be read skeptically.

Dosage Guidelines

Experience LevelDosage Range
Beginner1020 mg/day
Intermediate2030 mg/day
Advanced3030 mg/day
Frequency
Daily oral, split into 3-4 doses due to the short (~4 hour) half-life. Some users switch to injectable (reportedly ~5-10mg) or sublingual dosing to bypass first-pass metabolism and improve bioavailability, community-reported, not clinically verified.
Typical Cycle Length
68 weeks
Notes

All human dosing/PK figures here are community- and vendor-derived, no published human pharmacokinetic or clinical trial exists for SR9009. Oral bioavailability is reportedly very poor due to first-pass hepatic metabolism (community estimates put it in the low single-digit percent range), which is why users split doses through the day or seek injectable/sublingual routes.

Half-Life

Widely cited community/vendor estimate; no published human pharmacokinetic study exists for SR9009.

Side Effects

Insomnia

uncommon
Severity
2/5

May disrupt sleep if taken too late in the day.

Mitigation

Avoid doses in the evening.

Wakefulness

common
Severity
1/5

Increased alertness and energy.

Mitigation

Generally considered a benefit; time doses appropriately.

General Mitigation Strategies

Avoid late-day dosing to prevent sleep disruption. Injectable form is more bioavailable but less convenient.

Post Cycle Therapy (PCT)

PCT Not Required

Not hormonal. No PCT required.

How It Works

SR9009 binds to Rev-Erb proteins, which are involved in circadian rhythm regulation and metabolism. This increases mitochondrial activity, enhances glucose and fatty acid oxidation, and improves exercise capacity.

Fundamentals

Reference on the practices relevant to Stenabolic: how they are done and where they go wrong. Not a recommendation to use it.

Common Stacks

  • Stenabolic + Cardarine - Maximum endurance (with cancer risk caveats)
  • Stenabolic + SARMs - Enhanced cutting

WADA Status

Prohibited by WADA
Category: S4. Hormone and Metabolic Modulators
In-Competition: ProhibitedOut-of-Competition: Prohibited

SR9009 (Stenabolic) is explicitly prohibited at all times as a metabolic modulator under S4.4.1 (Rev-erbα agonists, e.g. SR9009, SR9011) on the 2026 WADA Prohibited List.

References

Last updated: July 18, 2026