SLU-PP-332

ID: slupp332

Aliases: SLU-PP332, pan-ERR agonist, SLU-PP-332

Type: compound

Route/form: oral or route depends on studied product

Status: research

Evidence level: preclinical

Best data tier: non-human experimental

Support scope: non-human/mechanistic

Source types: preclinical

Linked sources: 5

Broad outcomes: Fat loss / metabolic health, Longevity / mitochondrial / redox, Muscle growth / performance / recovery

Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.

Targets / mechanism

Optimization domains

Research basis

Limits, risks, and missing evidence

Risk flags

Linked papers, labels, and reviews

  1. Synthetic ERR alpha/beta/gamma agonist induces an acute aerobic exercise response
    preclinical / pubmed_slupp332_2023
    SLU-PP-332 mouse and cell work.
  2. A synthetic ERR agonist alleviates metabolic syndrome
    preclinical / pubmed_slupp332_metabolic_syndrome_2024
    SLU-PP-332 preclinical metabolic-syndrome model; adjacent to exercise-mimetic and fat-oxidation rationale.
  3. Chemical optimization of the exercise mimetic SLU-PP-332
    preclinical / sciencedirect_slupp332_sar_2026
    2026 SAR paper.
  4. An orally active estrogen receptor-related receptor agonist, SLU-PP-915, enhances aerobic exercise capacity
    preclinical / pubmed_slupp915_exercise_2026
    Orally active pan-ERR agonist follow-on to SLU-PP-332; useful class/mechanism context, still non-human efficacy.
  5. Novel pan-ERR agonists ameliorate heart failure through enhancing cardiac fatty acid metabolism and mitochondrial function
    preclinical / pubmed_panerr_agonists_heart_failure_2024
    ERR agonist tissue-metabolism context; supports mitochondrial/fatty-acid oxidation mechanism but not human enhancement use.