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TMP778

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  • ¥2045 - 8000
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-102075A
  • 2025年07月05日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • 规格

      10 mM * 1 mL/1 mg/5 mg/10 mg

    规格:10 mM * 1 mL产品价格:¥4900.0
    规格:1 mg产品价格:¥2045.0
    规格:5 mg产品价格:¥4500.0
    规格:10 mg产品价格:¥8000.0

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    TMP778

    CAS No. : 1422053-04-0

    MCE 国际站:TMP778

    产品活性:TMP778 是一种有效的、RORγt 的选择性逆向激动剂,其 FRET 检测出的 IC50 值为 7 nM。

    研究领域:Metabolic Enzyme/Protease  |  Vitamin D Related/Nuclear Receptor

    作用靶点:ROR

    In Vitro: It is found that TMP778 at >2.5 μM starts to show toxic effects on cell growth, which however is not RORγt-dependent, since the proliferation of RORγt-deficient T cells cultured under Th17 cell-polarizing conditions is also decreased. Otherwise, these inhibitors do not show inhibitory effects on cell proliferation or RORγt expression or its nuclear translocation, but efficiently inhibited IL-17 production. TMP778 has a much broader dose range and efficiently decreased IL-17 production, consistent with its higher binding affinity for RORγt. These data indicate that TMP778 is the RORγt inhibitor that most potently reduced IL-17 production.

    In Vivo: All three compounds (e.g., TMP778) delay the onset of disease and substantially reduce the severity of disease progression compared to control-treated mice. Consistent with in vitro results, TMP778 treatment causes the most pronounced effect on the disease phenotype. This treatment not only decreases the number of mononuclear cells infiltrating the central nervous system (CNS), but also most strongly reduces the percentage of IL-17+ T cells in the CNS (including IL-17+ IFNγ+). There is no significant change in the percentage IFNγ+ IL-17-T cells in the CNS among all groups, indicating that none of the inhibitors affects Th1 responses. TMP778 strongly inhibits Th17 cell generation, reduces IL-17 production from differentiated Th17 cells, and also dramatically ameliorates the progression of EAE.

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