SLU-PP-332 - SLU-PP-332 is an estrogen-related receptor (ERR) pan-agonist

SLU-PP-332

SLU-PP-332 is an estrogen-related receptor (ERR) pan-agonist studied as an exercise mimetic that boosts mitochondrial activity and fat oxidation.

Fat LossEnergy
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100 capsules × 250 mcg · 25000 mcg total

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Total Price

฿2900

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For research & laboratory use only. Not for human consumption.

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Half-Life

~1-3 hours

Administration Route

Subcutaneous injection

Exercise Mimetic

Activates ERR alpha to mimic endurance-exercise metabolism

Fat Oxidation

Up-regulates fatty-acid oxidation and energy expenditure

Endurance

Improves mitochondrial function and running endurance in models

Effect Timeline

Start - Week 2

Increased energy expenditure and fat utilisation

Week 4

Improved endurance and metabolic markers

Week 8

Sustained mitochondrial and body-composition effects

Mechanism of Action

SLU-PP-332 is a synthetic small-molecule agonist of the estrogen-related receptors ERR alpha, ERR beta and ERR gamma, orphan nuclear receptors that act as master regulators of oxidative metabolism. Activating these receptors upregulates the PGC-1 alpha transcriptional program, driving mitochondrial biogenesis and a shift toward fatty-acid oxidation in skeletal muscle. The result mimics several adaptations of endurance exercise: higher oxidative-fibre activity, increased running capacity in preclinical models, and elevated whole-body energy expenditure without raising food intake. Because it works upstream through nuclear-receptor transcription rather than appetite suppression, SLU-PP-332 is studied as an exercise-mimetic approach to fat metabolism and metabolic endurance distinct from incretin agonists.

Why Researchers Choose SLU-PP-332

SLU-PP-332 is an estrogen-related receptor (ERR) pan-agonist studied as an exercise mimetic, a compound that reproduces metabolic adaptations of endurance training without physical activity. By activating ERR alpha, beta and gamma, it amplifies the PGC-1 alpha program that governs how muscle and other oxidative tissues generate energy. Research interest centres on:

  • Mitochondrial biogenesis and oxidative-metabolism upregulation
  • Exercise-mimetic modelling: increased running capacity and endurance in preclinical work
  • Fat oxidation and energy-expenditure protocols that do not rely on appetite suppression
  • Skeletal-muscle fibre-type and metabolic-flexibility research
  • Comparison against incretin agonists for fat-mass reduction with preserved food intake

Because SLU-PP-332 acts upstream through nuclear-receptor transcription, it offers a mechanistically distinct route to fat metabolism and metabolic endurance compared with GLP-1 or GLP-1/GIP peptides.

ERR Signalling and Energy Expenditure

ERR receptors are orphan nuclear receptors that coordinate the transcription of genes for oxidative phosphorylation, mitochondrial assembly and fatty-acid catabolism. When SLU-PP-332 engages them:

  1. The PGC-1 alpha coactivator program is amplified, the same pathway endurance exercise recruits
  2. Mitochondrial biogenesis increases the cell’s oxidative capacity
  3. Metabolism shifts toward fatty-acid oxidation, favouring fat as fuel
  4. Whole-body energy expenditure rises while food intake stays unchanged in preclinical models

The net effect studied is a fat-mass reduction driven by burning more energy rather than eating less.

Reconstitution and Storage

Reconstitution: reconstitute the vial with bacteriostatic water (1 to 2ml); swirl gently until dissolved, do not shake. Keep capsules in a cool, dry place away from light. After reconstitution: hold refrigerated and use within 28 days.

For research purposes only. Not for human consumption.

Vial & calculation

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