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PCCR-1

Chemical Structure : PCCR-1

CAS No.: 1820667-82-0

PCCR-1 (RORγ inhibitor PCCR-1)

Catalog No.: PC-38747Not For Human Use, Lab Use Only.

PCCR-1 is a potent, specific RORγ inhibitor with binding IC50 of 34.45 nM and 778.1 nM for human and mouse RORγ, respectively, > 300-fold selectivity over other isoforms of ROR.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    PCCR-1 is a potent, specific RORγ inhibitor with binding IC50 of 34.45 nM and 778.1 nM for human and mouse RORγ, respectively, > 300-fold selectivity over other isoforms of ROR.
    PCCR-1 demonstrates promising potency for IL-17A inhibition in human and canine PBMCs and mouse splenocytes with no significant impact on Th1 and Th2 cytokines.
    PCCR-1 exhibits significant efficacy in the acute CS model with dose-dependent inhibition of the PD biomarkers, effectively inhibited IL-17A release in whole blood and BALf samples from COPD patients.

    Physicochemical Properties

    M.Wt 541.614
    Formula C28H29F2N3O4S
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20°C 12 Months; 4°C 6 Months
    In Solvent
    -80°C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    N-(2-(2-(2,4-difluorophenoxy)propan-2-yl)-1-ethyl-1H-benzo[d]imidazol-5-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide

    References

    1. Desai H, et al. Sci Rep. 2022 May 24;12(1):8744.

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