SLU-PP-915

guinea pig

Also seen as: SLU-PP915, SLU PP 915, slu

The Dose Guy’s verdict
Sep 1, 2026
4 sources

Skip it for now. SLU-PP-915 is the second-generation exercise mimetic from the ERR agonist family, a follow-on to SLU-PP-332 with better oral activity in mice and the same zero human mileage. The mechanism is genuinely interesting, telling cells to build mitochondria and burn fat the way training does, but nobody has tested it in a person. Watch the ERR space; do not volunteer as the trial.

Would I take it?Not yet. Zero human data.

What it is

A small molecule that activates all three estrogen-related receptors: ERR-alpha, ERR-beta, and ERR-gamma. Those receptors are the metabolic switches that flip when you exercise hard, driving mitochondrial biogenesis and fat oxidation in muscle and heart. SLU-PP-915 came out of the same Saint Louis University lab that built SLU-PP-332, redesigned to survive the gut and work when swallowed, where the original needed injection to reach useful blood levels.

The mouse work is clean. Oral SLU-PP-915 boosted exercise capacity, lit up the right gene targets, and both SLU-PP-915 and SLU-PP-332 improved cardiac function in a heart-failure model. But mice absorbing a research chemical and running farther on a treadmill is the opening chapter, not the ending. Human liver microsome work identified metabolites, but nobody has dosed a person. No safety profile, no efficacy signal in people. If weight loss is the actual goal, retatrutide and tirzepatide are a different planet of evidence.

What the research shows

No human trials. Zero. Everything below is animal or in-vitro work. Read it as “interesting,” not “evidence it works in you.”

All cells and mice. No human trial of any kind.

SLU-PP-915 increased expression of the ERR target genes PGC-1alpha, LDHA, DDIT4, and PDK4 in gene-expression assays.Eur J Med Chem 2023 · discovery
Mice given oral SLU-PP-915 ran as far as those given injections, once you adjust for how much actually reached the blood.JPET 2026 · mice
SLU-PP-915 and SLU-PP-332 both improved ejection fraction and survival in a pressure-overload heart-failure model.Circulation 2024 · mice
Human liver S9 and microsome experiments identified seven phase-I transformation products of SLU-PP-915 and no phase-II products.Rapid Commun Mass Spectrom 2026 · human liver in vitro
No human trial or safety study of SLU-PP-915 exists.as of Aug 2026

Realistic protocols

I’m not writing a dose for a compound with zero human data. The only metabolism work is in vitro: human liver S9 and microsome assays found seven phase-I transformation products and no phase-II products, which means nobody knows how your liver actually handles this at a real dose, how fast it clears, or what the metabolites do. If you run it anyway: source with a COA, start as low as you can measure, keep the run short, log everything, and get bloodwork before and after. You are the experiment, and there is no literature to bail you out if something goes wrong.

Side effects

No human has reported a side effect under controlled conditions:

unknownNo human safety data of any kind exists. ERR agonism drives mitochondrial biogenesis and metabolic gene expression across tissues, and nobody has measured what pharmacological activation does to a person over weeks or months. A mouse tolerating something is not evidence that you will.

Where to buy

$2.50 / 20mg vial$0.12/mg
✓ verified Sep 12

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