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AF-399 42016530

Chemical Structure : AF-399 42016530

CAS No.: 618864-56-5

AF-399 42016530 (AF-399/42016530)

Catalog No.: PC-61466Not For Human Use, Lab Use Only.

AF-399/42016530 is a potent CCR4 antagonist that blocked CCL22- and CCL17-mediated migration of human peripheral blood CD4+CD25+ Treg and Th2 cells ex-vivo and murine Tregs in-vivo.

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

    Biological Activity

    AF-399/42016530 is a potent CCR4 antagonist that blocked CCL22- and CCL17-mediated migration of human peripheral blood CD4+CD25+ Treg and Th2 cells ex-vivo and murine Tregs in-vivo.
    AF-399/42016530 enhances DC-mediated human CD4(+) T cell proliferation in an in vitro immune response model and amplifies cellular and humoral immune responses in vivo in experimental models.
    AF-399/42016530 induces antigen-specific CD8+ T cells and tumor immunity against self antigens in combination with vaccines.

    Physicochemical Properties

    M.Wt 531.619
    Formula C26H17N3O4S3
    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

    4-(1-benzofuran-2-ylcarbonyl)-1-[5-(benzylsulfanyl)-1,3,4-thiadiazol-2-yl]-3-hydroxy-5-(2-thienyl)-1,5-dihydro-2H-pyrrol-2-one.

    References

    1. Klein A, et al. Oncotarget. 2017 May 9;8(19):31079-31091.

    2. Bayry J, et al. Proc Natl Acad Sci U S A. 2008 Jul 22;105(29):10221-6.

    3. Pere H, et al. Blood. 2011 Nov 3;118(18):4853-62.

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