
1 / 3Growth Factor & Tissue Signaling Research · Oral Research Compounds
$168.00$84.00Save 50%
SLU-PP-332 is a synthetic small-molecule pan-agonist of the estrogen-related receptors ERRα, ERRβ and ERRγ, a family of orphan nuclear receptors first characterized in academic pharmacology programs. Although it is catalogued alongside research peptides, it is an orally formulated small molecule that appears in published work on ERR-mediated transcription, mitochondrial biogenesis pathways and oxidative metabolism gene programs in cell and animal models.
Real Peptides supplies SLU-PP-332 as capsules in a 100 count bottle, finished in the United States. Every batch is assayed by an independent laboratory, and the certificate of analysis for the current lot is published in the lab results section so it can be reviewed before purchase. Orders ship from Florida and California within 24 hours. Material is sold for laboratory research use only and is not for human or animal consumption.
Quantity
$84.00
SLU-PP-332 Capsules — 100 count · 250mcg (100 Capsules)
$84.00$168.00
For Research Use Only. Not for human or veterinary use. Not for use in diagnostic or therapeutic procedures. Not for food, drug, or cosmetic use.
99% Pure | 100 Capsules | Finished in the USA
SLU-PP-332 is a small-molecule pan-agonist of the estrogen-related receptors (ERRα, ERRβ, ERRγ), a family of orphan nuclear receptors. It appears in published research examining ERR-mediated transcription, mitochondrial biogenesis pathways, and oxidative metabolism gene programs in model systems.
For Research Use Only. Not for human or veterinary use.

SLU-PP-332 is a small-molecule agonist of the estrogen-related receptor family — ERRα, ERRβ, and ERRγ. It was developed at Saint Louis University, from which it takes its name.
ERRs are orphan nuclear receptors: they have no identified endogenous ligand, which historically made them difficult to study pharmacologically. Synthetic agonists such as SLU-PP-332 are therefore valuable research tools. Published work examines ERR-mediated transcription, mitochondrial biogenesis pathways, and oxidative metabolism gene programs in skeletal muscle cell models.


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