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UM-259 is a STING inhibitor with an EC50 of 1.50 μM in THP1-Dual cells expressing wild-type STING. It 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-259 can be used to study STING-dependent inflammation and neurological disorders.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | UM-259 is a STING inhibitor with an EC50 of 1.50 μM in THP1-Dual cells expressing wild-type STING. It 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-259 can be used to study STING-dependent inflammation and neurological disorders. |
| In vitro | UM-259 (0.2-5 μM, pretreated for 1 hour) effectively inhibits diABZI-induced IFNβ and IL6 gene transcription in iBMDMs. Additionally, UM-259 (2.5 μM, pretreated for 1 hour) demonstrates strong activity in blocking STING-dependent IFNβ secretion in primary human CD14+ monocytes. Moreover, UM-259 (5 μM, pretreated for 1 hour) significantly inhibits diABZI-induced TBK1 and IRF3 phosphorylation, efficiently suppressing STING oligomerization and downstream signaling in WT BMDMs. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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