Skip to main content
4 views

SLU PP 332

SLU PP 332 molecular structure

Overview

SLU PP 332 is an experimental small molecule exercise mimetic that activates estrogen-related receptor (ERR) signaling pathways, particularly ERRα, ERRβ, and ERRγ, which play crucial roles in mitochondrial biogenesis and oxidative metabolism. ERRs are key regulators of genes involved in energy production and fatty acid oxidation, normally activated by exercise. Research demonstrates SLU PP 332 increases mitochondrial content, enhances oxidative capacity, improves endurance performance, and promotes fat oxidation in animal models without actual exercise. The compound effectively recapitulates some molecular signatures of endurance training. Studies show potential applications for obesity, metabolic syndrome, muscular dystrophies, and conditions where exercise is limited or impossible. SLU PP 332 represents a novel approach to exercise mimicry distinct from AMPK activators like AICAR. The compound is in early research stages with limited published human data. It holds promise for conditions where exercise prescription is challenging, though questions remain about whether pharmacological exercise mimicry can fully replicate the comprehensive benefits of physical activity.

Last reviewed: 2026-08-18

Identity & Aliases

Also known as

SLU-PP-332SLU PP 332ERR pan-agonist

Status: Research compound - Exercise mimetic

CAS303760-60-3
PubChem5338394

Full composition (formula, molecular weight, sequence) in Quick Facts →

Research Areas

Exercise mimetics / enduranceEstrogen-related receptor (ERR) signalingMitochondrial biogenesisMetabolic syndrome (preclinical)

Available Evidence

Animal

In mice, SLU-PP-332 induced an ERRα-dependent acute aerobic exercise response and enhanced exercise capacity (ACS Chem Biol 2023). A separate mouse study found the ERR agonist alleviated metabolic-syndrome features including fatty liver, cholesterol, and weight gain (J Pharmacol Exp Ther 2024).

In Vitro

In cell assays, SLU-PP-332 activates ERRα, ERRβ, and ERRγ and upregulates oxidative-metabolism and mitochondrial genes.

Uncertain

Claims that it 'mimics exercise' in humans are speculative: all functional evidence is from rodents, and poor oral bioavailability has been reported.

Key Studies & Findings

2 studies
Preclinical2023

A synthetic ERRα/β/γ agonist (SLU-PP-332) induced an ERRα-dependent acute aerobic exercise response and enhanced exercise capacity in mice.

Benefits & Effects

6 documented

Enhanced endurance

anecdotal

Fat burning

anecdotal

Metabolic activation

anecdotal

Mitochondrial biogenesis

anecdotal

Energy enhancement

anecdotal

Exercise mimetic effects

anecdotal

Side Effects & Safety

2 reported

Limited safety data available

Unknown

Early-stage research compound

Unknown

Limitations & Open Questions

All evidence is preclinical (rodent); there are no human safety, pharmacokinetic, or efficacy data. Bioavailability and dosing are unresolved, and long-term effects of ERR pathway activation are unknown.

Pharmacology

Pan-agonist of estrogen-related receptors (ERRα/β/γ) that drives expression of mitochondrial and oxidative-metabolism genes; in rodent studies typically administered by injection, with poor oral bioavailability reported.

Reported Research Dosing

Reported values from research literature and community protocols. Educational reference only — not a dosing recommendation or medical advice.

Research protocols under development - dosage not yet established

Half-life: Unknown (early research stage)

Research Protocols

RESEARCH USE ONLY - Standard metabolic protocol

Dose
50 mg/kg (animal dosing)
Frequency
Twice daily
Route
Intraperitoneal injection (IP)

RESEARCH USE ONLY - Acute exercise enhancement

Dose
50 mg/kg (animal dosing)
Frequency
Single dose 1 hour pre-exercise
Route
Intraperitoneal injection (IP)

RESEARCH USE ONLY - Extended treatment

Dose
50 mg/kg (animal dosing)
Frequency
Twice daily for 4-8 weeks
Route
Intraperitoneal injection (IP)

HUMAN DOSING NOT ESTABLISHED

Dose
No approved human dose
Frequency
Awaiting clinical trials
Route
Oral formulation in development

Research protocols are for educational purposes only. Always consult qualified medical professionals.

Frequently Asked Questions

Has SLU-PP-332 been tested in humans?

No. Published studies are limited to mice and cell assays.

Does SLU-PP-332 actually improve endurance?

In mice it increased exercise capacity and metabolic fitness; no human data exist.

Research Citations

1
A Synthetic ERR Agonist Alleviates Metabolic Syndrome.

Billon C, Schoepke E, Avdagic A, Chatterjee A, Butler AA, Elgendy B, Walker JK, Burris TP (2024)

2
Novel Pan-ERR Agonists Ameliorate Heart Failure Through Enhancing Cardiac Fatty Acid Metabolism and Mitochondrial Function.

Xu W, Billon C, Li H, Wilderman A, Qi L, Graves A, Rideb JRDC, Zhao Y, Hayes M, Yu K, Losby M, Hampton CS, Adeyemi CM, Hong SJ, Nasiotis E, Fu C, Oh TG, Fan W, Downes M, Welch RD, Evans RM, Milosavljevic A, Walker JK, Jensen BC, Pei L, Burris T, Zhang L (2024)

3
Synthetic ERRα/β/γ Agonist Induces an ERRα-Dependent Acute Aerobic Exercise Response and Enhances Exercise Capacity.

Billon C, Sitaula S, Banerjee S, Welch R, Elgendy B, Hegazy L, Oh TG, Kazantzis M, Chatterjee A, Chrivia J, Hayes ME, Xu W, Hamilton A, Huss JM, Zhang L, Walker JK, Downes M, Evans RM, Burris TP (2023)

4
Estrogen-Related Receptor Agonism Reverses Mitochondrial Dysfunction and Inflammation in the Aging Kidney.

Wang XX, Myakala K, Libby AE, Krawczyk E, Panov J, Jones BA, Bhasin K, Shults N, Qi Y, Krausz KW, Zerfas PM, Takahashi S, Daneshpajouhnejad P, Titievsky A, Taranenko E, Billon C, Chatterjee A, Elgendy B, Walker JK, Albanese C, Kopp JB, Rosenberg AZ, Gonzalez FJ, Guha U, Brodsky L, Burris TP, Levi M (2023)

5
Targeting ERRs to counteract age-related muscle atrophy associated with physical inactivity: a pilot study.

Bonanni R, Falvino A, Matticari A, Rinaldi AM, D'Arcangelo G, Cifelli P, Iundusi R, Gasbarra E, Tancredi V, Cariati I, Tarantino U (2025)

+ 4 more citations

Related Resources

Quick Facts

Formula

C18H14N2O2

Molecular Weight

500.0

Mechanism

Activates AMPK and ERR pathways to mimic exercise-induced metabolic changes

Safety Information

Early-stage research compound. Safety profile under investigation.

View All Peptides