$80

Peptides
SLU-PP-332
ERRα/β/γ Pan-Agonist (St. Louis University). Supplied as a lyophilised powder in 5mg vials.
Supplied as lyophilised powder in a 5mg specification. Storage: -20°C · Protect from light · Keep dry. Dispatched from Sydney, Australia-wide.
Product information
About SLU-PP-332
ERRα/β/γ Pan-Agonist (St. Louis University)
Research background as published in the scientific literature. Supplied for in-vitro laboratory research only; nothing here is a claim about use in humans or animals.
SLU-PP-332 is a synthetic compound developed by researchers at Saint Louis University as a pan-agonist of the Estrogen Related Receptor family (ERRα, ERRβ, ERRγ). ERRs are orphan nuclear receptors that regulate networks of genes involved in mitochondrial biogenesis, fatty acid oxidation, and oxidative phosphorylation.
Preclinical research has investigated SLU-PP-332 as a potential exercise mimetic, with rodent studies reporting activation of molecular pathways associated with endurance adaptations. The compound represents a research tool for studying ERR biology and mitochondrial metabolic regulation.
- Type
- Synthetic small molecule / ERR pan-agonist
- Research Areas
- Mitochondrial biogenesis, oxidative metabolism, exercise mimetics
- Molecular Formula
- C23H22N2O3
- Molecular Weight
- 378.4 g/mol
- Developer
- Saint Louis University research group
- Key Pathways
- ERRα/γ · PGC-1α · Mitochondrial biogenesis
- Primary Research
- Oxidative metabolism, exercise mimetics
- Research Models
- Rodent metabolic and endurance models
- 01ERRα / ERRγ Pan-AgonismSLU-PP-332 was developed as a pan-agonist of the Estrogen Related Receptors α, β, and γ. Research examines its binding affinity and transcriptional activation across ERR subtypes, which regulate mitochondrial biogenesis and oxidative metabolism gene networks.
- 02Mitochondrial BiogenesisLaboratory studies have investigated SLU-PP-332's effects on PGC-1α co-activation and downstream mitochondrial gene expression. Animal studies report increases in mitochondrial density and oxidative capacity in skeletal and cardiac muscle tissue models.
- 03Exercise Mimetic PathwaysResearch has examined whether SLU-PP-332 can activate metabolic adaptations typically associated with endurance exercise at the molecular level. Studies in rodent models have reported improvements in running performance and metabolic markers without training.
References
- 1Zuercher WJ et al. Discovery of ERR pan-agonists. J Med Chem. 2005;48(9):3107-9.
- 2Brown EL et al. SLU-PP-332 exercise mimetic study. J Pharmacol Exp Ther. 2023.
- 3PubMed: pubmed.ncbi.nlm.nih.gov/?term=SLU-PP-332
- 4Giguere V. Transcriptional control of energy homeostasis by ERRs. Endocr Rev. 2008.
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