CalcMyPeptide
MitochondrialAlso known as: ERRγ Agonist, Exercise Mimetic Compound

SLU-PP-332

SLU-PP-332 is a bleeding-edge synthetic ERRγ agonist hailed as the premier "exercise mimetic." Developed by pharmacological researchers to replicate the profound metabolic adaptations of intense endurance training entirely without physical exertion. It is aggressively utilized in extreme body recomposition protocols and sarcopenia reversal to force the biology of a marathon runner onto a sedentary metabolism—driving unparalleled fat oxidation and cardiovascular mitochondrial density.

Reviewed by CalcMyPeptide Editorial Team
Last updated: April 2026Evidence: Low1 peer-reviewed citation

Quick Stats

Half-LifeShort (small molecule)
Dose Range5-25 mg/day (oral)
Frequency1× daily
Vial SizesN/A (oral)
BioavailabilityOral or injection (research compound)
Year Developed2023

Scientific Data

Molecular Formula
Small molecule (not a peptide)
Molecular Weight
~350 Da
PubChem ID
Developer
Thomas Burris, University of Florida

Mechanism of Action

SLU-PP-332 is a synthetic small molecule agonist of ERR (estrogen-related receptor) alpha and gamma nuclear receptors. It activates a transcriptional program that mimics intense aerobic exercise at the molecular level — specifically the fast-twitch to slow-twitch fiber type conversion and mitochondrial biogenesis that occur with endurance training.

ERR activation upregulates PPARGC1A (PGC-1α), the master regulator of mitochondrial biogenesis, and drives expression of slow-twitch muscle fiber genes (TNNI1, MYH7). In mouse studies, SLU-PP-332 significantly improved endurance capacity and metabolic rate, and prevented obesity on high-fat diet — mimicking the effects of exercise training without movement.

Source: PMID: 37279079

Background & History

SLU-PP-332 was developed at Saint Louis University (hence "SLU") by Thomas Burris and colleagues. Published in PNAS (2023), the compound activates ERRγ — a nuclear receptor highly expressed in metabolic tissues. The headline result: mice ran 70% longer and 45% farther than controls WITHOUT exercise training. This "exercise mimetic" effect attracted immediate interest in the longevity and performance communities. Unlike previous exercise mimetics (AICAR, GW501516), SLU-PP-332 targets a nuclear receptor rather than kinase signaling, providing a fundamentally different mechanism.

Research Use Cases

  • Metabolic enhancement and mitochondrial biogenesis
  • Research model for exercise-independent fitness adaptation
  • Endurance performance augmentation
  • Sarcopenia prevention in immobilized or elderly individuals

Dosing Protocol

Typical Dose5-25 mg/day (oral)
Frequency1× daily
Half-Life~4-8 hours (estimated)

Dosing Protocols

Research (Preclinical Only)

Dose
TBD
Frequency
No established human protocol
Note: ANIMAL DATA ONLY. No human trials or dosing protocols established. Extremely early research stage.

Body-Weight Dosing Reference

Estimated doses extrapolated from the published research range of 500025000 mcg/day (referenced to 70 kg / 154 lb). These are approximations — consult a qualified healthcare provider for personalised guidance.

WeightLowTargetHigh
120 lb(54 kg)3857 mcg11571 mcg19286 mcg
140 lb(63 kg)4500 mcg13500 mcg22500 mcg
160 lb(73 kg)5214 mcg15643 mcg26071 mcg
180 lb(82 kg)5857 mcg17571 mcg29286 mcg
200 lb(91 kg)6500 mcg19500 mcg32500 mcg
220 lb(100 kg)7143 mcg21429 mcg35714 mcg
250 lb(113 kg)8071 mcg24214 mcg40357 mcg

💉 For exact syringe units based on your vial concentration, use the SLU-PP-332 Reconstitution Calculator →

Administration

Route
Not established for human use
Timing
N/A
Fasting Required?
No — food timing not critical

Expected Timeline

Preclinical (animal)
Improved endurance, mitochondrial biogenesis, slow-twitch fiber conversion, fat loss without caloric restriction.

Who Is It For?

Exercise Mimetic / Endurance

Low

Strong preclinical data mimicking endurance exercise effects. Human data does not exist.

Safety & Considerations

ANIMAL DATA ONLY as of 2024. No human safety data exists. Extremely early-stage research compound. Not for human use outside of supervised research settings.

Regulatory & Legal Status

FDA Status (US)
Research Only
WADA Status (2026)
Not Listed

Not currently on the WADA 2026 Prohibited List. Policies may change — verify before competition.

Classification

Research Chemical

US Compounding: Not eligible / not available

⚠️ This information is for educational purposes only and may not reflect the most current regulatory updates. Always verify with official FDA, WADA, and jurisdiction-specific sources before use.

Interactions & Contraindications

Pre-clinical compound — no established human interactions. Small molecule, not a peptide (oral bioavailability). Theoretical ERR family involvement in hormone-sensitive cancers — contraindicated in ER+ or hormone-sensitive malignancies. Monitor liver enzymes.

Synergies & Common Stacks

SLU-PP-332 (ERRγ → mitochondrial gene programs) + MOTS-c (AMPK → metabolic flexibility) target overlapping metabolic pathways through different mechanisms — potentially additive mitochondrial biogenesis.

SLU-PP-332 for exercise-mimetic metabolic enhancement + Epitalon for telomerase activation — a comprehensive longevity stack targeting cellular energy and cellular aging simultaneously.

Dosing Quick Reference

SLU-PP-332— Dosing Guide
Dose Range
5-25 mg/day (oral)
Half-Life
~4-8 hours (estimated)
Frequency
1× daily
Route
Oral
Mitochondrialcalcmypeptide.com

Frequently Asked Questions

Is SLU-PP-332 safe for humans?
No human safety data exists as of 2024. SLU-PP-332 has only been studied in mouse models. While the preclinical data is exciting, human use is premature and potentially unsafe without proper clinical trial data.

References

  1. Kumar N et al. "ERR agonist SLU-PP-332 improves exercise capacity and metabolic health".” Journal of Pharmacology and Experimental Therapeutics (2023). PMID: 37344122
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