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SLU-PP-332 is a synthetic small-molecule pan-ERR agonist that engages estrogen-related receptors ERRα, ERRβ, and ERRγ. With nanomolar potency, it enhances mitochondrial function, fatty acid oxidation, and oxidative metabolism. It is currently used in preclinical studies to explore metabolic regulation, mitochondrial health, and exercise-mimicking mechanisms in research models.
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SLU-PP-332 is a potent ERR agonist advancing research into metabolic regulation, exercise-mimetic pathways, mitochondrial health, and cardiovascular function. With demonstrated effects in multiple preclinical models, it provides a versatile platform for exploring the molecular underpinnings of energy metabolism and mitochondrial biology.[1]
In mouse studies, SLU-PP-332 significantly reduced weight gain and fat accumulation in diet-induced obesity models. Treated animals displayed improved glucose tolerance and insulin sensitivity, highlighting its potential as a research tool in energy metabolism and obesity mechanisms.[5]
Administration of SLU-PP-332 increased endurance in sedentary rodents, with studies reporting up to 70% longer running times and improved mitochondrial density.[6] This supports its use in research investigating exercise physiology and pharmacological exercise mimetics.
Studies show SLU-PP-332 reverses mitochondrial dysfunction in aged tissues, reduces oxidative stress, and restores autophagy and mitophagy processes.[7] These findings position it as a valuable compound for research into cellular aging, mitochondrial dynamics, and oxidative metabolism.
Preclinical data suggest SLU-PP-332 improves cardiac contractility, reduces fibrosis, and preserves energetic balance in heart failure models.⁸ These effects underscore its importance in research on cardiac energetics and myocardial resilience.
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