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Research & Educational Use Only. This protocol guide is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional before beginning any research protocol.
Rev-ErbA Agonist Evidence Grade: C (Animal Data)

SR-9009 (Stenabolic) Protocol Guide

⚠ No validated human dose. This compound is not FDA-approved and has no peer-reviewed human dose-finding trials. The figures below are research conventions extrapolated from preclinical (animal/in‑vitro) and community sources — not validated clinical dosing. Treat them as study references only. Research use only; not medical advice.

SR-9009 (Stenabolic) is a Rev-ErbA agonist developed at Scripps Research Institute. It is not a SARM but is often grouped with them. It modulates circadian rhythm genes, enhancing mitochondrial function, fat oxidation, and endurance. Despite impressive animal data, it has extremely poor oral bioavailability (~2%). This protocol covers various administration routes.

Protocol Overview

Compound
SR-9009 (Stenabolic)
Category
Rev-ErbA Agonist (Metabolic Modulator)
Mechanism
Activates Rev-ErbA alpha and beta nuclear receptors, modulating circadian rhythm gene expression. Increases mitochondrial count, enhances oxidative metabolism, reduces fat storage, and improves exercise endurance
Half-Life
4 hours
Form
Oral liquid, sublingual, or injectable
Route
Sublingual preferred (oral bioavailability ~2%)
Frequency
3-4x daily (split due to short half-life)
Cycle Length
8-12 weeks

Dosing Protocol

ProtocolDoseFrequencyRouteDuration
Oral (Low Bioavail.)20-30 mg3-4x daily (split)Oral8-12 weeks
Sublingual10-20 mg3x daily (split)Sublingual (hold 60s)8-12 weeks
Injectable10 mg2x dailySubcutaneous8-12 weeks

Expected Timeline

Week 1-2
Increased wakefulness and energy during active hours. Improved sleep quality. Subtle increase in exercise endurance.
Week 3-4
Noticeable fat loss, especially with caloric deficit. Cardio endurance significantly improved. Recovery between sessions improves.
Week 5-6
Peak metabolic effects. Reduced body fat with preserved lean mass. Cholesterol markers may improve (LDL reduction noted in studies).
Week 7-8
Continued fat oxidation. Exercise capacity remains elevated. No hormonal suppression (non-SARM).
Week 9-12
Sustained benefits without tolerance buildup. Can run longer cycles as it is non-hormonal and non-suppressive.

Side Effects & Monitoring

Common Side Effects

  • Wakefulness / difficulty sleeping if dosed too late
  • Injection site irritation (injectable form)
  • Mild headaches
  • Slightly increased heart rate during exercise

Precautions

  • Extremely poor oral bioavailability (~2%) - sublingual or injectable preferred
  • Does not suppress testosterone - no PCT needed
  • Frequent dosing required due to 4-hour half-life
  • Not a SARM despite being marketed alongside them
  • Banned by WADA for athletic competition

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Frequently Asked Questions

Why is SR-9009 oral bioavailability so low?

SR-9009 undergoes extensive first-pass metabolism in the liver, resulting in only ~2% reaching systemic circulation orally. This is why sublingual administration (holding under the tongue for 60+ seconds) or subcutaneous injection are preferred routes for meaningful blood levels.

Does SR-9009 suppress testosterone?

No. SR-9009 is not a SARM and does not interact with androgen receptors. It modulates Rev-ErbA circadian rhythm receptors. No PCT is needed, and it can be safely stacked with SARMs without adding suppression.

How does SR-9009 compare to Cardarine (GW-501516)?

Both enhance endurance and fat loss but through different mechanisms. SR-9009 modulates circadian genes and mitochondrial function, while GW-501516 activates PPARdelta. GW-501516 has much better oral bioavailability. They can be stacked for synergistic effects.

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⚠ Before any use: human safety data is limited or absent for many of these compounds. Consult a licensed healthcare provider first — especially if you are pregnant or nursing, have a medical condition, or take other medications.