Pan-ERR activation
Cell assays show agonist activity across ERRα, ERRβ, and ERRγ. These are nuclear receptors, distinct from classical estrogen receptors.
Pan-ERR Agonist • Oral Exercise-Mimetic Research
SLU-PP-915 is an orally active research compound that activates the estrogen-related receptors ERRα, ERRβ, and ERRγ. Mouse studies report changes in exercise-responsive genes and aerobic performance. It is a small molecule, not a peptide, and has no established human use.
SLU-PP-915 is a synthetic small molecule in a series of estrogen-related receptor (ERR) agonists. These receptors regulate transcription of genes involved in mitochondrial function, fuel use, and adaptation to aerobic exercise. Despite its place in peptide catalogs, SLU-PP-915 is not a peptide.
Its boronic-acid-containing thiophene scaffold differs from SLU-PP-332. Published work reports improved metabolic stability and measurable oral activity in mice. That is a research advantage, not evidence of a safe or effective human capsule.
Cell assays show agonist activity across ERRα, ERRβ, and ERRγ. These are nuclear receptors, distinct from classical estrogen receptors.
Studies found increased expression of ERR-regulated genes, including PGC-1α, PDK4, and Ddit4, in cells or mouse tissues.
ERR signaling coordinates mitochondrial and fatty-acid-oxidation programs. Gene responses suggest pathway engagement; they do not establish the same adaptations as training in people.
Unlike SLU-PP-332, SLU-PP-915 retained exercise-related activity after oral administration in mice when exposure was considered. Human absorption remains unknown.
The reported outcomes come from laboratory and mouse models. No published human trial has shown that SLU-PP-915 improves exercise capacity, metabolism, or cardiovascular outcomes.
Short mouse experiments reported greater running distance and duration after SLU-PP-915 exposure.
Mouse skeletal muscle showed an exercise-responsive gene signal that was sometimes comparable to treadmill running.
Mouse work found retained activity after oral administration at exposure-adjusted comparisons.
In a pressure-overload mouse model, SLU-PP-915 improved selected heart-function and fibrosis measures.
A 10–20 mg oral range is discussed in research communities, but published SLU-PP-915 dosing comes from animal experiments. No human schedule, cycle length, or route-specific safety profile has been established.
No human combination regimen has been validated. These pairings describe research questions and pathway overlap, not proven synergy.
One mouse study found stronger Ddit4 and mitochondrial gene responses alongside training. Human relevance is unknown.
SLU-PP-915 targets ERR signaling while O-304 activates AMPK. Their distinct metabolic pathways make this a research pairing; the combination has not been studied or shown to be beneficial.
Both appear in metabolic research, but they act through different pathways. Their combination has not been clinically tested.
There is no published human safety profile for SLU-PP-915. Short mouse experiments cannot rule out effects from prolonged ERR activation, different formulations, or higher exposure.
The relevant research is preclinical; no frequency or severity of human side effects can be estimated.
SLU-PP-915 is a useful step for ERR research because it retains oral activity in mice and has direct comparison data against SLU-PP-332. The exercise and cardiac findings make the pathway worth following.
The practical case for people is still unproven. No human trial has established a benefit, dose, or safety window, and a retail capsule cannot be assumed to match the study formulation. We grade the science as promising but the real-world evidence as early.
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