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首页-小分子抑制剂&激动剂-Nuclear Receptor/Transcription Factor-PPAR-DS-6930
DS-6930

Chemical Structure : DS-6930

CAS No.: 1242328-82-0

DS-6930 (DS 6930;DS6930)

货号: PC-35674Not For Human Use, Lab Use Only.

DS-6930 (DS 6930, DS6930) is a novel potent, selective PPARγ agonist with EC50 of 41 nM, Emax-68%.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

    生物&药学活性

    DS-6930 (DS 6930, DS6930) is a novel potent, selective PPARγ agonist with EC50 of 41 nM, Emax-68%.
    DS-6930 significantly recruits several cofactors, such as RIP140 and PGC1, in cofactor recruitment assays.
    DS-6930 demonstrates high PPARγ agonist potency with robust plasma glucose reduction, maintains diminished PPARγ-related adverse effects upon toxicological evaluation in vivo, and demonstrated no hepatotoxicity.

    物理化学性质&存储条件

    分子量 403.438
    分子式 C23H21N3O4
    外观性状 Solid
    CAS No.
    储存条件
    固体粉末
    -20 °C 12 个月; 4°C 6 个月
    配置液
    -80 °C 6 个月; -20°C 6 个月
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    3-((6-((3,5-dimethylpyridin-2-yl)oxy)-1-methyl-1H-benzo[d]imidazol-2-yl)methoxy)benzoic acid calcium salt

    参考文献

    1. Shinozuka T, et al. Bioorg Med Chem. 2018 Oct 1;26(18):5099-5117.

    2. Shinozuka T, et al. Bioorg Med Chem. 2018 Oct 1;26(18):5079-5098.

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