Short answer: SR9011 is an experimental REV-ERB agonist (a body-clock drug), not a SARM and not the same as Stenabolic (SR9009). It has only been studied in mice and cells: injected into mice, it raised energy use, lowered fat mass and changed sleep and activity patterns (Solt 2012). There is no researched human dosage; users report 10–30 mg a day split into several doses. Human side effects are not established, and it is banned in sport.

What is SR9011

SR9011 is a synthetic agonist of REV-ERB-alpha and REV-ERB-beta, nuclear receptors that help run the circadian clock and control metabolic genes in the liver, skeletal muscle and fat tissue. It was described in 2012 by researchers at the Scripps Research Institute together with its sister compound SR9009 (Solt 2012). The older version of this article called SR9011 “also known as Stenabolic” and a SARM; neither is correct. Stenabolic is SR9009, and neither compound acts on the androgen receptor.

The nickname “exercise in a bottle” comes from the mouse results below. For legality, sport and an overview, see our SR9011 review.

The Study & Development

The research behind SR9011 is all preclinical:

Study What it found Evidence
Solt 2012 A single injection shifted daily activity in mice; 10 days twice daily raised oxygen use about 5% while movement fell 15%; longer treatment reduced fat mass without changing food intake Animal
Banerjee 2014 REV-ERB agonists increased wakefulness, cut REM and deep sleep and reduced anxiety-like behavior in mice Animal
Sulli 2018 (Salk Institute) SR9009 and SR9011 killed several types of cancer cells and slowed brain tumors in mice, without affecting normal cells Cell / animal
Dierickx 2019 SR9009 changed cell survival and metabolism even in cells without REV-ERB, so effects are not all on-target Cell
Geldof 2016 Breakdown products of SR9011 mapped for anti-doping tests Lab

The older version of this article quoted a 50% increase in running capacity and 10–15 lb of fat loss in “studies”. We found no study with those numbers for SR9011, and no study in people at all.

SR9011 Benefits

  • Fat loss (mice): lower fat mass with longer treatment; food intake unchanged (Solt 2012). Not shown in people.
  • Energy use (mice): about 5% higher oxygen use (Solt 2012).
  • Endurance: activating REV-ERB-alpha increased exercise capacity in mice (Woldt 2013); not tested with SR9011 in people.
  • Anxiety (mice): less anxiety-like behavior with REV-ERB agonists (Banerjee 2014).
  • Muscle growth: not shown in any study we found.
  • Cholesterol and liver fat: lipid improvements were reported in obese mice given SR9009 (Solt 2012); not measured in people.

SR9011 Side Effects

Human side effects are not established, because no one has taken SR9011 in a study. What the research and user reports point to:

  • Sleep problems: users report insomnia; in mice, REV-ERB agonists increased wakefulness and cut REM and deep sleep (Banerjee 2014). The old claim that “4 out of 24 people” had insomnia had no source.
  • Unknown off-target effects: the sister compound changed cells that lacked its target (Dierickx 2019).
  • Liver: no SR9011 data, but SR9009 has been linked to acute liver failure needing a transplant in a 17-year-old (Shams Bin Shaheen 2026) and to liver injury in a 40-year-old man (Govil 2025).
  • Absorption: claims about poor oral bioavailability, and about skin products that fix it, have not been tested.

SR9011 For Women

There are no data on SR9011 in women. The old claim that it works the same in men and women “without the potential side effects” of steroids was not based on any study, and has been removed. Since SR9011 does not act on the androgen receptor, masculinizing effects would not be expected, but its other effects, including on sleep and the liver, are simply unknown.

Dosage

There is no researched human dose. In mice, effective doses were around 50–100 mg per kg of body weight by injection, which cannot be converted into a safe human dose (Solt 2012). The half-life in people is not established; the old figure of about four hours had no source.

Commonly reported (anecdotal) Daily amount
Lower range 10 mg, split
Middle range 20 mg, split
Upper range 30 mg, split into three doses

These are what users describe, not tested or recommended doses. Users avoid evening doses because of sleep problems. For the sister compound, see SR9009 dosage.

Bulking & Cutting Stacks:

No SR9011 stack has been studied. Users describe pairing it with MK-677 or LGD-4033 on a bulk and with RAD-140, ostarine or AC-262 on a cut. The partner compounds have their own documented effects: ostarine and LGD-4033 lowered testosterone and HDL in trials (Dalton 2011, Basaria 2013), MK-677 raised appetite and blood sugar, RAD-140 raised liver enzymes in most patients in its trial (LoRusso 2022), and AC-262 has only rat data. Check any combination with the stack checker and read RAD-140 stacks.

Conclusion:

SR9011 is a research tool for the body clock with interesting mouse results (more energy use, less fat, altered sleep, anti-cancer effects in cells) and no human data. Its dose, half-life, absorption and side effects in people are unknown, and its sister compound SR9009 has been linked to serious liver injury. WADA bans SR9011 at all times (WADA 2026), and in Australia it is Schedule 4 with possession controls (Poisons Standard). Compare it with better-studied compounds in the SARMs database.

Frequently asked questions

Is SR9011 the same as Stenabolic?

No, Stenabolic is SR9009Evidence: Lab

Stenabolic is SR9009. SR9011 is a closely related REV-ERB agonist described in the same 2012 study.

Read the full section

What is the SR9011 dosage?

No researched human doseEvidence: User reports

There is no researched human dose; users report 10–30 mg a day, which is anecdotal. Mouse doses were around 50–100 mg/kg by injection.

Read the full section

What are the side effects of SR9011?

Not established in peopleEvidence: Limited

Users report insomnia, which fits mouse data showing more wakefulness with REV-ERB agonists. Its sister compound SR9009 has been linked to serious liver injury.

Read the full section

Does SR9011 burn fat?

In mice; untested in peopleEvidence: Animal

In mice, longer treatment reduced fat mass and raised energy use without changing food intake. No study has tested fat loss in people.

Read the full section

Can women take SR9011?

No data in womenEvidence: Limited

There are no data in women. It does not act on the androgen receptor, but its other effects are unknown in anyone.

Read the full section

Sources

  1. Regulation of circadian behaviour and metabolism by synthetic REV-ERB agonists 2012 · PMID 22460951
  2. Pharmacological targeting of the mammalian clock regulates sleep architecture and emotional behaviour 2014 · PMID 25536025
  3. Pharmacological activation of REV-ERBs is lethal in cancer and oncogene-induced senescence 2018 · PMID 29320480
  4. SR9009 has REV-ERB-independent effects on cell proliferation and metabolism 2019 · PMID 31127047
  5. In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011 2016 · PMID 27706103
  6. Rev-erb-α modulates skeletal muscle oxidative capacity by regulating mitochondrial biogenesis and autophagy 2013 · PMID 23852339
  7. Acute Liver Failure in an Adolescent Following Use of the Synthetic REV-ERB Agonist SR9009 2026 · PMID 42750938
  8. When Gains Go Wrong: A Case of Selective Androgen Receptor Modulator-Related Liver Injury 2025 · PMID 40765588
  9. The selective androgen receptor modulator GTx-024 (enobosarm) improves lean body mass and physical function in healthy elderly men and postmenopausal women: results of a double-blind, placebo-controlled phase II trial 2011 · PMID 22031847
  10. The safety, pharmacokinetics, and effects of LGD-4033, a novel nonsteroidal oral, selective androgen receptor modulator, in healthy young men 2013 · PMID 22459616
  11. A First-in-Human Phase 1 Study of a Novel Selective Androgen Receptor Modulator (SARM), RAD140, in ER+/HER2- Metastatic Breast Cancer 2022 · PMID 34565686
  12. WADA: The Prohibited List (2026 List, in force from 1 January 2026) 2026
  13. Therapeutic Goods (Poisons Standard—June 2026) Instrument 2026 (F2026L00633) 2026
  14. PubChem: SR9011 (CID 57394021), names and synonyms 2026