REGULATORYRFK Jr.: 14 peptides returning to Category 1 — FDA advisory committee July 2026TRENDINGHexarelin: ↑↑ Surging ��� Trends score 100 as of May 2026UPDATESemaglutide and tirzepatide compounding ended — shortage resolved Feb/May 2025REGULATORYBPC-157, TB-500, thymosin alpha-1, CJC-1295, ipamorelin: expected Category 1 reclassification pendingEVENTpep-talk con ��� First US Peptide Convention · August 2026 · Anaheim CAFDAFDA advisory committee meetings scheduled: late July 2026REGULATORYRFK Jr.: 14 peptides returning to Category 1 — FDA advisory committee July 2026TRENDINGHexarelin: ↑↑ Surging ��� Trends score 100 as of May 2026UPDATESemaglutide and tirzepatide compounding ended — shortage resolved Feb/May 2025REGULATORYBPC-157, TB-500, thymosin alpha-1, CJC-1295, ipamorelin: expected Category 1 reclassification pendingEVENTpep-talk con ��� First US Peptide Convention · August 2026 · Anaheim CAFDAFDA advisory committee meetings scheduled: late July 2026

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Peptide Library

SLU-PP-332

ERR alpha agonist

Weight Loss & Metabolic

SLU-PP-332 is a small molecule agonist of the estrogen-related receptors (ERRs), particularly ERR-alpha and ERR-gamma, developed at Saint Louis University as an exercise mimetic that enhances muscle endurance and fatigue resistance without physical training. It is not technically a peptide but a synthetic small molecule that activates transcription factors controlling mitochondrial biogenesis, oxidative metabolism, and muscle fiber type composition. Published in 2023, it represents one of the newest entries in the exercise mimetic compound class and remains in very early preclinical development.

Mechanism of Action

ERRa agonist that mimics the transcriptional effects of exercise. Activates mitochondrial biogenesis and oxidative metabolism pathways.

Research Protocols

For research purposes only. Not medical advice.

Research protocols limited to animal studies. Mouse models used 25-50mg/kg. No established human dosing.

Research Notes

Clinical Research Status

SLU-PP-332 was first published in the Journal of Pharmacology and Experimental Therapeutics in 2023 by researchers at Saint Louis University, representing extremely early-stage preclinical research with only animal data available. No clinical trials have been registered or planned for human testing, and the compound remains purely a research tool for understanding ERR biology and exercise physiology. Its emergence has generated media attention as a potential "exercise in a pill" compound, though such applications remain speculative and distant from clinical reality.

Key Published Findings

Mouse studies demonstrate that SLU-PP-332 administration increased running endurance by approximately 50% on treadmill exhaustion tests and enhanced fatigue-resistant oxidative (Type I and IIa) muscle fiber proportions without exercise training. The compound activates ERR-alpha and ERR-gamma transcription factors, which are master regulators of mitochondrial biogenesis, fatty acid oxidation, and oxidative phosphorylation gene programs in skeletal muscle. Treated animals showed increased muscle mitochondrial density, enhanced oxidative capacity, and gene expression profiles resembling those of trained athletes.

Safety Profile

Formal toxicology studies have not been published, and the safety profile of SLU-PP-332 in any species is largely unknown beyond the limited animal experiments reported. ERR receptors are expressed in multiple tissues including heart, kidney, and brain, raising theoretical concerns about off-target effects from systemic ERR activation. The structural novelty of the compound means there is no existing clinical safety data from related molecules to extrapolate from, unlike older exercise mimetics with more established safety profiles.

Comparison to Related Compounds

SLU-PP-332 targets a different pathway than AICAR (AMPK activation) or GW501516 (PPAR-delta activation), representing a third distinct molecular approach to exercise mimicry through the ERR transcription factor family. While GW501516 demonstrated concerning carcinogenicity in long-term animal studies, whether ERR agonism carries similar risks is unknown due to the early stage of research. Unlike both AICAR and GW501516 which have years of research history and some human data, SLU-PP-332 has only a single primary publication and minimal characterization.

Community Observations

Interest in SLU-PP-332 has been driven primarily by mainstream media coverage framing it as an "exercise pill," generating excitement in fitness and longevity communities. The compound is not commercially available from any legitimate source as of current reports, and anyone claiming to sell it likely cannot verify identity or purity. Experienced researchers in the performance enhancement space advise patience, noting that the journey from initial publication to any form of human-ready compound typically spans 10-15 years of development.

Half-Life

~4-6 hours

Reconstitution

DMSO or appropriate vehicle

Storage

Lyophilized

Store at -20C. Protect from light and moisture.

Reconstituted

Store at -20C in solution.

US Legal Status

Research chemical (not FDA-approved)

Also Known As

ERR alpha agonist

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