
SR-9009 (stenabolic)
MetabolicPreclinicalAlso known as: SR9009, Stenabolic, SR-9009, Rev-erb agonist SR9009
SR-9009, sold as stenabolic, is a synthetic agonist of the nuclear receptors REV-ERB-alpha and REV-ERB-beta. It came out of Thomas Burris and Theodore Kamenecka laboratory work at the Scripps Research Institute and was first described in a 2012 Nature paper as a tool for pharmacologically shifting the circadian clock and the metabolism it controls (PMID: 22460951).
Overview
At A Glance
SR-9009 is a synthetic agonist at REV-ERB-alpha (NR1D1) and REV-ERB-beta (NR1D2), heme-binding nuclear receptors that act as transcriptional repressors within the core circadian clock. Agonist binding increases their repressive activity on target promoters, altering the daily exp…
Overview
SR-9009, sold as stenabolic, is a synthetic agonist of the nuclear receptors REV-ERB-alpha and REV-ERB-beta. It came out of Thomas Burris and Theodore Kamenecka laboratory work at the Scripps Research Institute and was first described in a 2012 Nature paper as a tool for pharmacologically shifting the circadian clock and the metabolism it controls (PMID: 22460951). It was never a pharmaceutical company development candidate, has never entered human trials, and has no approval anywhere. Anti-doping laboratories describe it plainly as a compound that failed to reach FDA approval and whose illegal distribution raised concern (PMID: 38735208). REV-ERB proteins sit inside the core circadian clock and repress the genes that drive the daily cycle of activity and fuel use. Activating them with a drug changes the timing and level of metabolic gene expression in liver, muscle and fat. In the original mouse work this raised energy expenditure, and in diet-induced obese mice it reduced fat mass with drops in plasma cholesterol, triglycerides, free fatty acids and glucose (PMID: 22460951). A separate group showed that REV-ERB-alpha controls mitochondrial biogenesis in oxidative muscle and that pharmacological activation increased exercise capacity in mice (PMID: 23852339). There is a serious problem with the mechanism story. When researchers built mice lacking both REV-ERB-alpha and REV-ERB-beta, SR-9009 still reduced cell viability, rewired cellular metabolism and altered gene transcription in cells that had no target left to act on. The authors concluded that the effects of SR-9009 cannot be used as a stand-in for REV-ERB activity (PMID: 31127047). In other words, some of what the compound does in cells is off-target, and which of the metabolic effects are REV-ERB-dependent is unsettled. There are no human data of any kind. No pharmacokinetics, no safety study, no efficacy trial. In the mouse studies that produced the metabolic results, the compound was given by intraperitoneal injection rather than by mouth (PMID: 22460951), which matters because SR-9009 is sold as an oral liquid and as capsules. It is prohibited in sport. WADA lists Rev-erb-alpha agonists including SR9009 and SR9011 under section S4.4, metabolic modulators, and horse and camel racing authorities have developed detection methods for it (PMID: 38735208; PMID: 42530886). When 44 products marketed online as SARMs were chemically analyzed, SR9009 was one of the unapproved drugs found in products that did not list it on the label (PMID: 29183075). What is sold as stenabolic, in liquid or capsule form, is a research chemical with no pharmacopoeial standard, no established human dose and no published human exposure. Buyers are the first humans on record taking it, and there is no monitoring of what happens next.
Potential Research Fields
Chemical Information
IUPAC Name
Not yet available
CAS Number
1379686-30-2
Molecular Formula
C20H24ClN3O4S
Molecular Mass
437.94 g/mol
Dosing & Protocols
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Interactions
Contraindications
No human data exist, so no evidence-based contraindications can be stated. Mechanism-based caution applies to anyone with a circadian or sleep disorder, since the drug is designed to shift clock gene expression (PMID: 22460951), and the documented REV-ERB-independent cytotoxicity in cell studies is an unresolved safety question (PMID: 31127047). Prohibited at all times in tested human and equine sport (PMID: 38735208).
Research Disclaimer
This interaction data is compiled from published research and community reports. It may not be exhaustive. Always consult a healthcare professional before combining compounds.
$59.99
up to $79.99
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1
2
capsule, liquid
| Vendor | Product | Form | Qty | Price | $/mg | Coupon | |
|---|---|---|---|---|---|---|---|
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SR-9009 capsules (60) | capsule | 60 capsules● In Stock | $59.99BEST | — | — | |
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SR-9009 30 mg/mL | liquid | 1 vial (30 mg/mL)● In Stock | $79.99 | — | — |
Tracking since Sep 7, 2026 · 2 data points
Vendors Selling SR-9009 (stenabolic)
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Every supplier above is graded 0–100 on COA verification, payment transparency, shipping, reviews, and active listings. Methodology published, no pay-to-rank.
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Protocols, calculator & safety for SR-9009 (stenabolic)
Research Score
0 PubMed studies
Quality Indicators
Data Completeness
63%Quick Facts
Half-Life
Not established in humans; no human pharmacokinetic study has been published. In the mouse experiments that produced the metabolic findings the compound was given by intraperitoneal injection rather than orally (PMID: 22460951)
Molecular Weight
437.94 g/mol
Administration
Intraperitoneal injection (rodent studies), Oral (as sold on the research chemical market)
CAS Number
1379686-30-2
Trial Phase
Preclinical
Research Disclaimer
This information is for educational and research purposes only. Not intended as medical advice. Consult a healthcare professional before use.
Frequently Asked Questions
What is SR-9009 (stenabolic) used for in research?
SR-9009, sold as stenabolic, is a synthetic agonist of the nuclear receptors REV-ERB-alpha and REV-ERB-beta. It came out of Thomas Burris and Theodore Kamenecka laboratory work at the Scripps Research Institute and was first described in a 2012 Nature paper as a tool for pharmacologically shifting the circadian clock and the metabolism it controls (PMID: 22460951). It was never a pharmaceutical company development candidate, has never entered human trials, and has no approval anywhere. Anti-doping laboratories describe it plainly as a compound that failed to reach FDA approval and whose illegal distribution raised concern (PMID: 38735208).
REV-ERB proteins sit inside the core circadian clock and repress the genes that drive the daily cycle of activity and fuel use. Activating them with a drug changes the timing and level of metabolic gene expression in liver, muscle and fat. In the original mouse work this raised energy expenditure, and in diet-induced obese mice it reduced fat mass with drops in plasma cholesterol, triglycerides, free fatty acids and glucose (PMID: 22460951). A separate group showed that REV-ERB-alpha controls mitochondrial biogenesis in oxidative muscle and that pharmacological activation increased exercise capacity in mice (PMID: 23852339).
There is a serious problem with the mechanism story. When researchers built mice lacking both REV-ERB-alpha and REV-ERB-beta, SR-9009 still reduced cell viability, rewired cellular metabolism and altered gene transcription in cells that had no target left to act on. The authors concluded that the effects of SR-9009 cannot be used as a stand-in for REV-ERB activity (PMID: 31127047). In other words, some of what the compound does in cells is off-target, and which of the metabolic effects are REV-ERB-dependent is unsettled.
There are no human data of any kind. No pharmacokinetics, no safety study, no efficacy trial. In the mouse studies that produced the metabolic results, the compound was given by intraperitoneal injection rather than by mouth (PMID: 22460951), which matters because SR-9009 is sold as an oral liquid and as capsules.
It is prohibited in sport. WADA lists Rev-erb-alpha agonists including SR9009 and SR9011 under section S4.4, metabolic modulators, and horse and camel racing authorities have developed detection methods for it (PMID: 38735208; PMID: 42530886). When 44 products marketed online as SARMs were chemically analyzed, SR9009 was one of the unapproved drugs found in products that did not list it on the label (PMID: 29183075).
What is sold as stenabolic, in liquid or capsule form, is a research chemical with no pharmacopoeial standard, no established human dose and no published human exposure. Buyers are the first humans on record taking it, and there is no monitoring of what happens next.
What forms does SR-9009 (stenabolic) come in?
SR-9009 (stenabolic) is available in capsule, liquid forms.
How much does SR-9009 (stenabolic) cost?
Prices start at $59.99 across 1 verified vendor.
How do I compare SR-9009 (stenabolic) vendors?
Compare prices, payment methods, shipping, and COA scores across 1 vendor.
Research Tools
Related Compounds
View AllAICAR (acadesine)
MetabolicPhase 3AICAR is a nucleoside analog of adenosine.
Amlexanox
MetabolicFDA ApprovedAmlexanox is an old anti-inflammatory drug with a second life.
Berberine
MetabolicPreclinicalBerberine is an isoquinoline alkaloid — a naturally occurring plant secondary metabolite with a characteristic yellow color — extracted from the roots, rhizomes, stems, and bark of several plant genera including Berberis (barberry, Oregon grape), Coptis (goldthread), Hydrastis (goldenseal), Phellodendron (Amur cork tree), and Tinospora (guduchi).
Cardarine (GW501516)
MetabolicDiscontinuedCardarine is the market name for GW501516, a synthetic agonist of the nuclear receptor PPAR-delta developed by GlaxoSmithKline as a treatment for low HDL cholesterol and the lipid problems that travel with metabolic syndrome.
Metformin
MetabolicPreclinicalMetformin is a biguanide-class oral antihyperglycemic medication that has been in continuous clinical use since 1957 (in France under the brand name Glucophage) and is now the most-prescribed diabetes medication worldwide with over 150 million prescriptions annually.
SLU-PP-915
MetabolicPreclinicalSLU-PP-915 is an experimental agonist of the estrogen-related receptors, a family of three orphan nuclear receptors called ERR-alpha, ERR-beta and ERR-gamma that control genes for mitochondrial biogenesis, oxidative phosphorylation, fatty acid oxidation and the Krebs cycle.
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