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Evidence review

SLU-PP-332: The "Exercise Pill" Sold as a Peptide (It Isn't One)

SLU-PP-332 is a small molecule, not a peptide. Mice ran 70% longer on injections; no human has taken it in a trial, and its makers say it isn't orally absorbed.

Written by Derek OlssonSports Science Editor

SLU-PP-332 is not a peptide, and no human has taken it in a published trial. It is a small synthetic molecule, 290 daltons with the formula C18H14N2O2, and it contains no amino-acid chain at all10. It switches on a family of proteins called estrogen-related receptors (ERRs), and in mice it made sedentary animals run about 70% longer1. That is the whole evidence base for the "exercise pill" label: rodents, injected into the abdomen, twice a day.

The finding that went the wrong way is about how it is sold. Some sellers offer it as a capsule. In 2026, the same research group that created SLU-PP-332 wrote that it "lacks oral bioavailability," and built a different compound, SLU-PP-915, to fix that5. A search of ClinicalTrials.gov for SLU-PP-332 returns zero registered studies11.

The study vs the bottle

Swipe to view all columns

In the studiesIn a buyer's hands
Who took itMiceA person (never trialed)
RouteInjection into the abdomenOften capsules; not orally absorbed
Dose50 mg/kg, twice a dayNone established
How long7 to 28 daysOpen-ended
Safety recordNo overt toxicity in 10 daysNo human data
Sources: Billon 2023 (ACS Chem Biol), Billon 2024 and 2026 (J Pharmacol Exp Ther), ClinicalTrials.gov.

What SLU-PP-332 actually does

The name sounds hormonal, and it is not. Estrogen-related receptors are "orphan" nuclear receptors, meaning no natural hormone is known to switch them on, and despite the name they are not estrogen receptors1. They sit inside cells and turn on genes for mitochondria, fat burning and the energy cycle. Exercise raises their activity in muscle, which is why a drug that switches them on directly looked like a shortcut.

SLU-PP-332 was designed for that job as a laboratory tool. The developers' first paper describes it as having "sufficient pharmacokinetic properties to be used as an in vivo chemical tool"1, which is a precise phrase: good enough to dose mice, not a drug candidate. A 2026 chemistry paper calls it "a well-established exercise mimetic and widely used chemical probe," and reports newer versions with better solubility and metabolic stability14. The research field has already moved past it. The compound sold online is the prototype.

What the two mouse papers measured

Paper one (2023): the endurance result. Researchers in St. Louis reported SLU-PP-332 as a "pan agonist" that activates all three ERRs, most strongly ERR-alpha1. In muscle cells it raised mitochondrial function. In mice, it shifted muscle toward oxidative type IIa fibers. Sedentary mice given 50 mg/kg by intraperitoneal injection twice a day for seven days ran about 70% longer and 45% farther on a treadmill than mice given a placebo injection1. The effect depended on ERR-alpha.

Paper two (2024): the weight result. The same group gave obese mice the same dose, by the same route, for 28 days2. The mice burned more energy and more fat, gained far less fat mass, and improved insulin sensitivity. Diet-induced obese mice on the drug weighed about 12% less after 28 days. The study in genetically obese mice was cut to 12 days "due to reduced tolerance of twice per day intraperitoneal administration"2.

Follow-up work has stayed in animals and dishes:

  • Heart. In mice with heart failure induced by pressure overload, SLU-PP-332 and its sister compound improved ejection fraction, reduced scarring and increased survival3.
  • Kidney. In 21-month-old mice, eight weeks of SLU-PP-332 reversed age-related protein leakage in the urine, loss of filtering cells and kidney inflammation4.
  • The successor. SLU-PP-915, built because SLU-PP-332 is not absorbed by mouth, matched its endurance effect in mice when swallowed, and further raised exercise-linked muscle gene activity when combined with treadmill training5. One 2025 study used muscle samples from 20 women having hip surgery, but the drug only touched cells in a dish, not the women6.

A 2026 systematic review of the whole literature said the same thing in its conclusion: "Clinical trials are needed to confirm their efficacy and safety in humans"13.

Why "exercise mimetic" does not mean what the label implies

"Exercise mimetic" is a lab term for a compound that switches on some of the same genes exercise does. It is not a promise that a person gets fitter without training. The phrase has been here before. In 2008, AICAR made sedentary mice run 44% longer after four weeks, and its authors called it an exercise mimetic too12. It never became an approved endurance drug.

Three gaps sit between the mouse data and a capsule bought online:

  • Dose. 50 mg/kg twice a day in a mouse does not translate into a human dose by simple arithmetic, and nobody has run the human dose-finding study that would.
  • Route. Every endurance and weight result used intraperitoneal injection. The developers' own 2026 paper says SLU-PP-332 is not orally bioavailable5.
  • What is in the bottle. With no approved product and no reference standard sold to consumers, a buyer cannot confirm the contents. Our guide to vendor red flags covers why a certificate of analysis from the seller does not settle that.

For how this compares with the other two compounds sold on the same promise, see MOTS-c and endurance, which is at least a real peptide your own cells make, and 5-Amino-1MQ, another small molecule sold on peptide shelves.

What is actually known

  • Activates ERRs in cellsSTRONG evidence

    Shown repeatedly in cell assays.

  • Longer running in sedentary miceMODERATE evidence

    About 70% longer; one research group.

  • Less fat gain in obese miceMODERATE evidence

    Same group, same injected dose.

  • Works when swallowedNONE evidence

    Its developers say it lacks oral bioavailability.

  • Human endurance or weight lossNONE evidence

    Zero registered trials.

  • Safe in humansNONE evidence

    No human safety data exists.

Side effects: unknown in humans, so the honest list is short

There is no human safety data. That is not a figure of speech: no trial, no case series, no adverse event database entry tied to a known dose.

What the mouse papers report is narrow. The 2023 paper saw "no overt toxicity" over 10 days at the study dose, with normal blood counts, electrolytes and creatine kinase1. The 2024 paper shortened one arm because the obese mice tolerated the twice-daily injections poorly2.

Two things are known about how the human body handles it, both from liver tissue in test tubes. Anti-doping labs incubated SLU-PP-332 with human liver fractions and found 9 to 22 breakdown products, depending on the lab and method78. Those studies exist to catch athletes, not to establish safety.

ERRs also run energy metabolism in the heart and kidney, which is why those mouse studies exist34. Effects there were favorable in diseased mice. Nobody knows what years of ERR activation do to a healthy human heart.

Why it shows up on peptide shelves

SLU-PP-332 reached the peptide market for the same reason 5-Amino-1MQ did: the same research-chemical sites sell both, under a "for research use only" label, to the same buyers who come for BPC-157 and MOTS-c. Nothing about the chemistry connects them. A research-use label is not a quality standard, and it is not permission to take the product. Our explainer on where peptides are sold and what the research-chemical label means covers why that label exists and what it does not protect.

If you are weighing it anyway, these are the questions that have no answer yet:

  • What dose, if any, is active in a person?
  • Does anything reach the blood when it is swallowed?
  • What does it do to the heart, liver and kidneys over months?
  • Is the powder in the capsule actually SLU-PP-332, and how much of it?

Until a human study answers the first three, the fourth is the only one a buyer can even try to check, and a seller's own test sheet cannot settle it.

Anti-doping status

Do not guess here; read the rule. SLU-PP-332 has no approval for human therapeutic use from any health authority anywhere, which is the trigger for WADA's S0 class of non-approved substances, prohibited at all times9. Anti-doping labs in Los Angeles and Cologne have already published methods to detect it, and the Cologne group describes it as having "doping potential"78. In plain terms: a tested athlete who takes it is taking a banned substance that labs are specifically looking for.

Run anything else you are considering through our prohibited-substance checker, and see the WADA list for peptides for how the classes work.

If what you want is a prescribed option

No licensed provider we review prescribes SLU-PP-332, and it has no route into a US compounding pharmacy: it is not an ingredient of any approved drug and is not on FDA's 503A bulks list. The closest thing a clinician will write is MOTS-c, the mitochondrial peptide sold on the same "exercise mimetic" pitch. Be clear about what that is: a compounded product, not FDA-approved, with mostly animal evidence, and banned in tested sport. Its regulatory picture is laid out in MOTS-c's FDA status.

What providers charge for it varies by more than double:

Every recovery-peptide provider we have checked is compared on our recovery peptide rankings.

The bottom line

SLU-PP-332 is an interesting research tool with good mouse data and nothing else. It is a small molecule, not a peptide. It worked by injection, not by mouth. It has never been tested in a person. And it is banned in sport, with detection methods already published. The "exercise pill" is, so far, a mouse that ran farther.

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Frequently asked questions

Is SLU-PP-332 a peptide?

No. It is a small synthetic molecule with a molecular weight of about 290, built to activate estrogen-related receptors. It is often listed beside peptides on research-chemical sites, but chemically it has nothing in common with them.

Does SLU-PP-332 work in humans?

Nobody knows. Every endurance and fat-loss result comes from mice given injections into the abdomen twice a day. ClinicalTrials.gov lists no registered human study, and a 2026 systematic review concluded that clinical trials are still needed.

What are the side effects of SLU-PP-332?

There is no human safety data. In mice, the developers saw no overt toxicity over 10 days at the study dose, and one group of obese mice tolerated twice-daily injections poorly enough that the study was shortened. Anything beyond that is guesswork.

Do SLU-PP-332 capsules work?

Its own developers wrote in 2026 that SLU-PP-332 lacks oral bioavailability, which is why they made a separate compound, SLU-PP-915, that can be taken by mouth. The mouse results all used injections.

Is SLU-PP-332 banned in sport?

It has no approval for human therapeutic use anywhere, which places it in WADA's S0 class of non-approved substances, prohibited at all times. Anti-doping labs have already published methods to detect it.

References

  1. Billon C, Sitaula S, Banerjee S, Welch R, et al. (2023). Synthetic ERRα/β/γ Agonist Induces an ERRα-Dependent Acute Aerobic Exercise Response and Enhances Exercise Capacity.. ACS Chem Biol. https://pubmed.ncbi.nlm.nih.gov/36988910/
  2. Billon C, Schoepke E, Avdagic A, Chatterjee A, et al. (2024). A Synthetic ERR Agonist Alleviates Metabolic Syndrome.. J Pharmacol Exp Ther. https://pubmed.ncbi.nlm.nih.gov/37739806/
  3. Xu W, Billon C, Li H, et al. (2024). Novel Pan-ERR Agonists Ameliorate Heart Failure Through Enhancing Cardiac Fatty Acid Metabolism and Mitochondrial Function.. Circulation. https://pubmed.ncbi.nlm.nih.gov/37961903/
  4. Wang XX, Myakala K, Libby AE, et al. (2023). Estrogen-Related Receptor Agonism Reverses Mitochondrial Dysfunction and Inflammation in the Aging Kidney.. Am J Pathol. https://pubmed.ncbi.nlm.nih.gov/37717940/
  5. Billon C, Appourchaux K, Côté I, Burris TP (2026). An orally active estrogen receptor-related receptor agonist, SLU-PP-915, enhances aerobic exercise capacity.. J Pharmacol Exp Ther. https://pubmed.ncbi.nlm.nih.gov/41421047/
  6. Bonanni R, Falvino A, Matticari A, et al. (2025). Targeting ERRs to counteract age-related muscle atrophy associated with physical inactivity: a pilot study.. Front Physiol. https://pubmed.ncbi.nlm.nih.gov/40692696/
  7. Avliyakulov NK, Sobolevsky T, Ahrens E, et al. (2026). Analysis and Identification of In Vitro Metabolites of Exercise Mimetic SLU-PP-332 ERRα/β/γ Agonist for Doping-Control Purposes.. Drug Test Anal. https://pubmed.ncbi.nlm.nih.gov/41688415/
  8. Möller T, Krug O, Thevis M, et al. (2026). In Vitro Metabolism and Analytical Characterization of SLU-PP-332 and SLU-PP-915: Novel Pan-ERR Agonists With Doping Potential.. Rapid Commun Mass Spectrom. https://pubmed.ncbi.nlm.nih.gov/41588687/
  9. World Anti-Doping Agency (2026). The Prohibited List (S0 Non-Approved Substances). WADA. https://www.wada-ama.org/en/prohibited-list
  10. National Center for Biotechnology Information (2026). SLU-PP-332, PubChem Compound CID 5338394 (molecular formula C18H14N2O2, molecular weight 290.3). PubChem. https://pubchem.ncbi.nlm.nih.gov/compound/5338394
  11. U.S. National Library of Medicine (2026). ClinicalTrials.gov search results for SLU-PP-332 (0 studies). ClinicalTrials.gov. https://clinicaltrials.gov/search?term=SLU-PP-332
  12. Narkar VA, Downes M, Yu RT, et al. (2008). AMPK and PPARdelta agonists are exercise mimetics.. Cell. https://pubmed.ncbi.nlm.nih.gov/18674809/
  13. de Souza-Lima J, Astrosa-Martin BD, Galaz-Rodríguez CA, et al. (2026). [Pharmacological Activation of ERRα/β/γ as an Exercise Mimetic: Potential Therapeutic Applications].. Rev Med Chil. https://pubmed.ncbi.nlm.nih.gov/42024694/
  14. Okda HE, Zhao P, Hayes M, et al. (2026). Chemical optimization of the exercise mimetic SLU-PP-332 enables insight into estrogen-related receptor signaling.. Int J Biol Macromol. https://pubmed.ncbi.nlm.nih.gov/41850449/

Medical disclaimer: This content is for general educational purposes only and is not medical advice, diagnosis, or treatment. Always consult a licensed healthcare professional before starting, stopping, or changing any treatment.