Stenabolic, SR-9009 · Evidence-based safety and harm-reduction overview.
| Also known as | Stenabolic, SR-9009 |
| Category | SARM |
| poor_bioavailability | Well-documented poor oral bioavailability, limiting efficacy of oral products |
| research_tool | Developed at Scripps as a scientific research probe, not intended for therapeutic use |
| rev_erb_agonist | Acts on nuclear Rev-erb proteins, not androgen receptors or traditional SARM pathways |
| US legal status | SR9009 is not approved by the FDA for any use, and it is illegal to market or sell it as a dietary supplement. Products are sold as research chemicals not for human consumption, and the FDA has warned that SARM-type products carry serious risks. It is prohibited at all times in sport under the WADA list. |
SR9009 (Stenabolic) is not a SARM but a Rev-erb agonist that influences circadian and metabolic pathways, and it is commonly grouped and sold with SARMs. It was developed as a research tool rather than a clinical drug.
SR9009 is a synthetic Rev-erb agonist that activates the nuclear Rev-erb alpha and beta receptors, which regulate circadian rhythm genes and metabolic pathways including lipid and glucose metabolism. It influences BMAL1, a key circadian-rhythm protein, and affects mitochondrial biogenesis. The compound was developed as a research probe, not as a therapeutic agent.
SR9009 (stenabolic) was developed by Dr. Thomas Burris and colleagues at The Scripps Research Institute as a tool to study Rev-erb biology and circadian metabolism. It was never intended for human use and no development toward clinical application occurred. The compound entered bodybuilding and performance-enhancement communities despite its research-only status and bioavailability limitations.
Research suggests SR9009 affects metabolism and endurance in animal studies by acting on Rev-erb proteins. A major limitation is that it has poor oral bioavailability, so much of the animal data used injection, and there are no human safety trials.
In animal studies, SR9009 was typically injected due to poor oral bioavailability; doses varied widely depending on experimental design. Oral bioavailability in humans is likely minimal to negligible, making oral products unlikely to produce the metabolic effects seen in injected animal studies. No human pharmacokinetics or dose studies exist.
This is general research/context information, not medical advice or a recommended protocol.
SR9009 is commonly marketed for stacking with SARMs or other compounds for enhanced fat loss and endurance. However, such combinations have never been studied and stacking multiplies unknown risks. The poor oral bioavailability of SR9009 itself raises questions about whether effects observed in stacks are genuine.
If you are going to research a compound, verifying identity and purity is the single most protective step. Independent analytical testing and sterile-handling supplies reduce risk.
Compare testing optionsIts poor oral bioavailability means oral products are unlikely to reach the levels that produced effects in injected animal studies.
No. It is a Rev-erb agonist, but it is commonly marketed and sold with SARMs.
We do not provide human dosing guidance. SR9009 is unapproved and any use should involve a qualified clinician.
It activates Rev-erb proteins that regulate BMAL1 and other circadian genes, theoretically shifting metabolic timing, but human effects are entirely unexplored.
No. Marketing claims sometimes suggest metabolic shortcuts, but animal work does not support such claims and no human evidence exists.
Medical & legal disclaimer. This site is for informational and harm-reduction purposes only. It is not medical advice and is not a substitute for a licensed healthcare professional. The compounds discussed are largely not approved by the FDA for human use and many are sold strictly as research chemicals 'not for human consumption.' Nothing here is an endorsement to purchase, possess, or use any substance. Laws vary by jurisdiction. Always consult a qualified physician and follow the law where you live.
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