1. Immunology/Inflammation
  2. STING IFNAR Interleukin Related
  3. UM-242

UM-242 是一种 STING 抑制剂,在表达野生型 STING 的 THP1-Dual 细胞中的 EC50 为 1.70 μM。UM-242 阻断 STING 寡聚化,抑制 diABZI 诱导的 TBK1IRF3 磷酸化,从而抑制 IFNβIL6 的转录,并减少 IFNβ 分泌。UM-242 可用于研究 STING 依赖性的炎症和神经系统疾病。

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UM-242

UM-242 Chemical Structure

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Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

UM-242 is a STING inhibitor, with an EC50 of 1.70 μM in THP1-Dual cells expressing wild-type STING. UM-242 blocks STING oligomerization and inhibits diABZI-induced phosphorylation of TBK1 and IRF3, thereby suppressing the transcription of IFNβ and IL6 and reducing IFNβ secretion. UM-242 can be used for the study of STING-dependent inflammatory and neurological diseases[1].

体外研究
(In Vitro)

UM-242 (0.2-5 μM,预处理 1 小时) 在 iBMDMs 中对 diABZI 诱导的 IFNβ 和 IL6 基因转录表现出强效抑制活性[1]
UM-242 (2.5 μM,预处理 1 小时) 在原代人 CD14+ 单核细胞中显示出阻断 STING 依赖性 IFNβ 分泌的强效活性[1]
UM-242 (5 μM,预处理 1 小时) 对 diABZI 诱导的 TBK1 和 IRF3 磷酸化表现出强效抑制活性,并在 WT BMDMs 中有效抑制 STING 寡聚化,显著阻断 STING 下游信号传导[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: WT BMDMs
Concentration: 5 μM
Incubation Time: Pretreated for 1 h
Result: Showed potent inhibitory activity on diABZI-induced phosphorylation of TBK1 and IRF3.
Exhibited potent activity in inhibiting STING oligomerization in WT BMDMs.
分子量

536.45

Formula

C24H18F2N8O5

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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UM-242
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HY-178047
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