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SLU-PP-915 CAS 2285432-92-8 ERR Agonist Metabolic Research

Product Name:SLU-PP-915

CAS:    2285432-92-8

MF:    C17H13BFNO3S

MW:    341.16

EINECS:    1592732-453-0

Appearance: Powder

Purity: ≥98%

Packaging: 1kg / 5kg / 10kg / 50kg / 100kg (custom packaging available)

Origin: China

    Brief Introduction

    Novel mitochondrial metabolism modulator
    Designed for advanced obesity & metabolic disorder research
    Potential thermogenic pathway activator
    High purity ≥98% (HPLC)
    Stable powder form, scalable synthesis
    Suitable for in vitro & preclinical studies
    Reliable bulk supply from China manufacturer
    Custom synthesis & COA available

    SLU-PP-915 (development code: 915) is a pan-estrogen-related receptor (pan-ERR) agonist developed by Saint Louis University and other institutions through a structure-based drug design approach . It is a next-generation compound structurally optimized from the well-studied SLU-PP-332, with the key improvement being the introduction of a boronic acid moiety that confers the critical advantage of oral bioavailability . SLU-PP-915 simultaneously activates all three ERR isoforms (α, β, and γ), regulating core metabolic processes such as mitochondrial biogenesis, fatty acid oxidation, and oxidative phosphorylation, and is regarded as a promising "exercise mimetic" .

    Key Scientific Value & Findings

    Oral Bioavailability - A Key Breakthrough: The first-generation compound SLU-PP-332, while effective, lacked oral bioavailability, limiting its application in chronic dosing studies . SLU-PP-915, through structural optimization (incorporating a boronic acid group), exhibits significantly improved metabolic stability, making it the first orally active, potent pan-ERR agonist .

    Enhanced Aerobic Exercise Capacity: Studies show that when administered intraperitoneally, SLU-PP-915 enhances aerobic exercise performance (distance and duration) in mice to an extent similar to SLU-PP-332. Importantly, this efficacy is maintained when administered orally after adjusting for systemic exposure, demonstrating excellent oral activity . This highlights its significant potential as an oral "exercise mimetic."

    Improved Cardiac Function in Heart Failure: In a mouse model of pressure overload-induced heart failure, treatment with SLU-PP-915 (and SLU-PP-332) significantly improved ejection fraction, ameliorated fibrosis, and increased survival without affecting cardiac hypertrophy . The mechanism involves transcriptional activation of metabolic gene networks involved in fatty acid metabolism and mitochondrial function, leading to substantial normalization of metabolic profiles for fatty acids/lipids and TCA/oxidative phosphorylation metabolites in the heart .

    Activation of ERR Target Genes: SLU-PP-915 potently upregulates the expression of ERR target genes such as DNA damage-inducible transcript 4 (Ddit4) , PGC-1α, lactate dehydrogenase A (LDHA), and pyruvate dehydrogenase kinase 4 (PDK4), which play central roles in energy metabolism of skeletal muscle and heart .

    Synergy with Exercise Training: Notably, SLU-PP-915 synergizes with actual exercise training to further enhance the expression of Ddit4 and mitochondrial genes . This provides a basis for studying the potential applications of combining pharmacological intervention with exercise.

    ERRγ as the Primary Mediator: In vitro and in vivo genetic dependency experiments have demonstrated that ERRγ is the primary mediator of ERR agonist-induced transcriptional regulation and cardioprotection .



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    Stable Supply, Consistent Quality: Leveraging robust Chinese manufacturing resources, we ensure stable delivery of bulk orders with consistent quality across all batches.

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      We provide COA (Certificate of Analysis) for each batch. Third-party testing is welcome

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