SLU-PP-332
Pan-ERR (estrogen-related receptor) agonist. Drives mitochondrial biogenesis + fatty-acid oxidation in skeletal muscle — preclinical 'exercise mimetic' candidate. Discovered + characterized at Saint Louis University (Burris lab).
How it clearsHalf cleared in ~6h. Most (~96%) gone by ~1d.
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Billman + Burris lab (Saint Louis University) published 2023 mouse data showing SLU-PP-332 administration produced exercise-mimetic effects: improved running endurance, mitochondrial biogenesis, fat oxidation — without exercise itself. The compound is a research tool — no human safety data, no clinical trials, no GMP supply chain. Grey-market product appearing in 2024-25 in biohacker forums is unverified material with no quality-control body. Frontier-tier speculative.
Frontier-tier speculative compound. Zero human safety data. Long-term ERR-agonism has un-modeled cardiac + metabolic concerns (the receptors are central regulators of cardiac energy metabolism). Identity verification of grey-market product is essentially impossible. Stack catalogs this for awareness + harm-reduction context, not endorsement. DIY use is a self-experiment of one with no off-ramp.
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- DMechanistic / anecdotal
SLU-PP-332 — primary mechanism: pan-err (estrogen-related receptor) agonist. drives mitochondrial biogenesis + fatty-acid oxidation in skeletal muscle — preclinical 'exercise mimetic' candidate. discovered + characterized at saint louis university (burris lab).
2 supporting referencesVerified 13d ago
External links to PubMed searches, ClinicalTrials.gov, and FDA materials. We do not host papers — we point at canonical sources.
Research tool only · no FDA pathway · grey-market product is unverified material
Pre-filled with this compound's published dose range: Unknown in humans (mouse: 10 mg/kg) · experimental — no human protocol
Draw volume exceeds 100 units (1 mL). Either reduce dose or split into multiple injections.
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