Skip to content
    Compare notes on r/BodyHackGuideCompare notes with other researchers. Join r/BodyHackGuide
    SR-9009 (stenabolic) molecular structure

    SR-9009 (stenabolic)

    MetabolicPreclinical

    Also 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).

    Disguised Alpha logo

    Lowest price

    $59.9960 capsules

    at Disguised Alpha

    Half-life: Not established in humansRoute: Intraperitoneal injection (rodent studies), Oral (as sold on…MW: 437.94 g/molCAS: 1379686-30-2
    Last reviewed:

    Overview

    At A Glance

    Mechanism

    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…

    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)
    Routes
    Intraperitoneal injection (rodent studies)Oral (as sold on the research chemical market)
    Potential Benefits
    Increased energy expenditure and reduced fat mass in diet-induced obese mice, with plasma cholesterol down 47 percent, triglycerides down 12 percent and glucose down 19 percent (PMID: 22460951)Increased exercise capacity in mice after pharmacological activation of Rev-erb-alpha, alongside greater muscle mitochondrial content (PMID: 23852339)Altered the circadian pattern of clock and metabolic gene expression in mouse hypothalamus, liver, muscle and adipose tissue (PMID: 22460951)Reduced weight gain and insulin resistance in mice exposed to constant light in a later rodent study (PMID: 39800061)

    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

    Circadian biologyNuclear receptor pharmacologyEnergy metabolismSports drug testing

    Chemical Information

    IUPAC Name

    Not yet available

    CAS Number

    1379686-30-2

    Molecular Formula

    C20H24ClN3O4S

    Molecular Mass

    437.94 g/mol

    Dosing & Protocols

    Unlock the Dosing tab

    Enter your email to keep reading. It is free, and it opens these tabs on every compound page in this browser.

    • Route

    You also get the free peptide cheat sheet by email. Unsubscribe anytime.

    Have an account? Sign in

    Research

    Unlock the research summary

    Enter your email to keep reading. It is free, and it opens these tabs on every compound page in this browser.

    • A summary of the key research
    • Safety and side effects
    • A link to the PubMed results

    You also get the free peptide cheat sheet by email. Unsubscribe anytime.

    Have an account? Sign in

    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.

    Best Price

    $59.99

    up to $79.99

    Best $/mg

    —

    Vendors

    1

    Listings

    2

    capsule, liquid

    Form
    Sort
    Vendor Product Form Qty Price $/mg Coupon
    Disguised Alpha logo
    Disguised Alpha
    50
    🇺🇸US🇪🇺EU🇬🇧UK
    SR-9009 capsules (60) capsule 60 capsules● In Stock $59.99BEST — —
    Disguised Alpha logo
    Disguised Alpha
    50
    🇺🇸US🇪🇺EU🇬🇧UK
    SR-9009 30 mg/mL liquid 1 vial (30 mg/mL)● In Stock $79.99 — —

    Sign in to leave a review

    Reviews on BodyHackGuide are tied to verified user accounts and moderated before publishing. Sign in (free, no spam) to share your experience with SR-9009 (stenabolic).

    Current low
    $59.99
    current listings
    7-day low
    —
    not enough history yet
    30-day low
    —
    not enough history yet
    30-day change
    —
    not enough history yet

    Tracking since Sep 7, 2026 · 2 data points

    Vendors Selling SR-9009 (stenabolic)

    How we score these vendors

    Every supplier above is graded 0 to 100 on COA verification, payment transparency, shipping, reviews, and active listings. Methodology published, no pay-to-rank.

    View Scorecard

    Related Compounds

    View All

    AICAR (acadesine)

    MetabolicPhase 3

    AICAR is a nucleoside analog of adenosine.

    t½ Intact acadesine was measurable in plasma for only about 2 hours after a short intravenous infusion in four healthy men, with total plasma clearance of 2.2 L/h/kg and negligible protein binding; radiolabeled drug-derived material had an apparent terminal half-life of about one week, reflecting metabolites rather than parent compound (PMID: 8227467)
    PreclinicalView Profile

    Amlexanox

    MetabolicFDA Approved

    Amlexanox is an old anti-inflammatory drug with a second life.

    t½ Not established in published human pharmacokinetic studies for the oral capsule form; a validated plasma assay has been used for preclinical pharmacokinetics in rats (PMID: 34842293)
    PreclinicalView Profile

    Berberine

    MetabolicPreclinical

    Berberine 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).

    PreclinicalView Profile

    Cardarine (GW501516)

    MetabolicDiscontinued

    Cardarine 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.

    t½ Not reported in the published human trials; the phase 1 and phase 2 studies described lipid outcomes over two to twelve weeks of oral dosing without publishing a terminal half-life (PMID: 17110604; PMID: 22814748)
    PreclinicalView Profile

    Metformin

    MetabolicPreclinical

    Metformin 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.

    PreclinicalView Profile

    SLU-PP-915

    MetabolicPreclinical

    SLU-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.

    t½ Not established in humans; in mice it is orally bioavailable and active by both oral and intraperitoneal routes, unlike its predecessor SLU-PP-332 (PMID: 41421047)
    PreclinicalView Profile

    View Full Dosage Guide →

    Protocols, calculator & safety for SR-9009 (stenabolic)

    Lowest Price

    Disguised Alpha logo

    Disguised Alpha

    $59.99

    1 vendor · 2 listings

    Research Score

    30

    0 PubMed results

    Quality Indicators

    Data Completeness

    63%
    Description
    Mechanism of Action
    Chemical Data
    Dosing Protocols
    Safety Profile
    PubMed Results
    Interactions
    Vendor Listings

    COA Verification

    0

    Verified COAs

    1

    Vendors w/ COA

    Latest test: 9/16/2026

    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 do I compare SR-9009 (stenabolic) vendors?

    Compare prices, payment methods, shipping, and COA scores across 1 vendor.

    How many vendors sell SR-9009 (stenabolic), and what does it cost per mg?

    1 of the vendors BodyHackGuide tracks list SR-9009 (stenabolic) (2 listings). The lowest listed price BodyHackGuide has recorded for SR-9009 (stenabolic) is $59.99. No SR-9009 (stenabolic) listing recorded as in stock carries a milligram count, so BodyHackGuide states no price per milligram for SR-9009 (stenabolic).

    Which vendors have third-party COAs for SR-9009 (stenabolic) on file at BodyHackGuide?

    BodyHackGuide holds 2 third-party certificate records for SR-9009 (stenabolic), from . No editor has read any of BodyHackGuide's 2 certificate records for SR-9009 (stenabolic). The laboratory named on BodyHackGuide's SR-9009 (stenabolic) certificate records is Freedom Diagnostics Testing, and the newest test date on them is 7 August 2026. Each vendor page on BodyHackGuide shows how many certificate records BodyHackGuide holds for that vendor and links to each record that has its own page.

    Research Tools

    You may also like

    Related Compounds

    View All

    AICAR (acadesine)

    MetabolicPhase 3

    AICAR is a nucleoside analog of adenosine.

    t½ Intact acadesine was measurable in plasma for only about 2 hours after a short intravenous infusion in four healthy men, with total plasma clearance of 2.2 L/h/kg and negligible protein binding; radiolabeled drug-derived material had an apparent terminal half-life of about one week, reflecting metabolites rather than parent compound (PMID: 8227467)
    PreclinicalView Profile

    Amlexanox

    MetabolicFDA Approved

    Amlexanox is an old anti-inflammatory drug with a second life.

    t½ Not established in published human pharmacokinetic studies for the oral capsule form; a validated plasma assay has been used for preclinical pharmacokinetics in rats (PMID: 34842293)
    PreclinicalView Profile

    Berberine

    MetabolicPreclinical

    Berberine 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).

    PreclinicalView Profile

    Cardarine (GW501516)

    MetabolicDiscontinued

    Cardarine 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.

    t½ Not reported in the published human trials; the phase 1 and phase 2 studies described lipid outcomes over two to twelve weeks of oral dosing without publishing a terminal half-life (PMID: 17110604; PMID: 22814748)
    PreclinicalView Profile

    Metformin

    MetabolicPreclinical

    Metformin 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.

    PreclinicalView Profile

    SLU-PP-915

    MetabolicPreclinical

    SLU-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.

    t½ Not established in humans; in mice it is orally bioavailable and active by both oral and intraperitoneal routes, unlike its predecessor SLU-PP-332 (PMID: 41421047)
    PreclinicalView Profile

    Free 2026 Peptide Cheat Sheet (PDF)

    38 compounds and blends: vial sizes, BAC water volumes, dosing ranges and bloodwork markers.

    Download Free

    Need bloodwork before starting?

    Full hormone + metabolic panels from Anabolic Insights. Code CHONCH for first-order discount.