Skip to content

Study · Not a test of the peptide alone · 2026

3 results

In Vitro Metabolism and Analytical Characterization of SLU-PP-332 and SLU-PP-915: Novel Pan-ERR Agonists With Doping Potential.

Möller T, Krug O, Thevis M

Rapid communications in mass spectrometry : RCM1 Apr 2026Cited by 2 (Europe PMC)

Summary

RationaleEstrogen-related receptor (ERR) agonists such as the drug candidates SLU-PP-332 and SLU-PP-915 are currently being investigated as exercise mimetics, given their ability to trigger human physiological processes similar to those initiated by actual physical activity. This capability prompted the consideration of these compounds as drugs potentially relevant for sports drug testing programs.MethodsThe two pan-ERR agonists SLU-PP-332 and SLU-PP-915 were characterized using liquid chromatography-high resolution (tandem) mass spectrometry (LC-HRMS/MS). Furthermore, the in vitro metabolic transformation products of both compounds prepared by means of human liver S9 fraction (S9 fraction) and human liver microsomes (HLMs) were analyzed. In addition, selected metabolites of SLU-PP-915 were synthesized and their structures were analyzed by nuclear magnetic resonance (NMR) spectroscopy.ResultsA total of nine metabolites were identified for SLU-PP-332, consisting of six Phase-I metabolites and three Phase-II conjugates. Conversely, the analysis of SLU-PP-915 yielded only Phase-I transformation products, with a total of seven metabolites identified. In both cases, an in-depth structural elucidation was conducted to obtain a comprehensive overview of the detected metabolites. Furthermore, three metabolites of SLU-PP-915 were confirmed through chemical synthesis and NMR.ConclusionThe results obtained in this study gave an in-depth view into the analysis and in vitro metabolism of the newly developed pan-ERR agonists SLU-PP-332 and SLU-PP-915. This may help to uncover the illicit use of these novel compounds as potential performance-enhancing substances.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study3

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone3

In this study, SLU-PP-332 was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking SLU-PP-332.

  1. 01LabNot a test of SLU-PP-332 aloneIn vitro (cell-free)Pharmacokinetics

    In human liver preparations, SLU‑PP‑332 yielded nine metabolites.

    In plain wordsIn lab tests, SLU‑PP‑332 yielded nine metabolites in human liver preparations.

    Peptide
    SLU-PP-332
    Outcome
    Not applicableIn vitro metabolite count
    Study

    humann: not reported in source

    Human liver S9 fraction and microsomes
    Outcome group
    Pharmacokinetics · Pharmacology

    Source sentences

    Summary
    A total of nine metabolites were identified for SLU-PP-332, consisting of six Phase-I metabolites and three Phase-II conjugates.
    1 context sentence
    Summary · context
    Furthermore, the in vitro metabolic transformation products of both compounds prepared by means of human liver S9 fraction (S9 fraction) and human liver microsomes (HLMs) were analyzed.

    In this study, SLU-PP-332 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking SLU-PP-332.

  2. 02LabNot a test of SLU-PP-332 aloneIn vitro (cell-free)Pharmacokinetics

    In human liver preparations, SLU‑PP‑332 yielded six Phase-I metabolites.

    In plain wordsIn lab tests, SLU‑PP‑332 yielded six Phase-I metabolites.

    Peptide
    SLU-PP-332
    Outcome
    Not applicablePhase-I metabolite count
    Study

    humann: not reported in source

    Human liver S9 fraction and microsomes
    Outcome group
    Pharmacokinetics · Pharmacology

    Source sentences

    Summary
    A total of nine metabolites were identified for SLU-PP-332, consisting of six Phase-I metabolites and three Phase-II conjugates.
    1 context sentence
    Summary · context
    Furthermore, the in vitro metabolic transformation products of both compounds prepared by means of human liver S9 fraction (S9 fraction) and human liver microsomes (HLMs) were analyzed.

    In this study, SLU-PP-332 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking SLU-PP-332.

  3. 03LabNot a test of SLU-PP-332 aloneIn vitro (cell-free)Pharmacokinetics

    In human liver preparations, SLU‑PP‑332 yielded three Phase-II conjugates.

    In plain wordsIn lab tests, SLU‑PP‑332 yielded three Phase-II conjugates.

    Peptide
    SLU-PP-332
    Outcome
    Not applicablePhase-II conjugate count
    Study

    humann: not reported in source

    Human liver S9 fraction and microsomes
    Outcome group
    Pharmacokinetics · Pharmacology

    Source sentences

    Summary
    A total of nine metabolites were identified for SLU-PP-332, consisting of six Phase-I metabolites and three Phase-II conjugates.
    1 context sentence
    Summary · context
    Furthermore, the in vitro metabolic transformation products of both compounds prepared by means of human liver S9 fraction (S9 fraction) and human liver microsomes (HLMs) were analyzed.

    In this study, SLU-PP-332 was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking SLU-PP-332.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    14 Oct 2026, 05:02 UTC

    Study results updated

  2. Version 1

    14 Oct 2026, 01:46 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.