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SR-717

Cat. No. M9923

All AbMole products are for research use only, cannot be used for human consumption.

SR-717 Structure
Synonym:

SR-717 lithium

Size Price Availability Quantity
1mg USD 70 In stock
5mg USD 150 In stock
10mg USD 220 In stock
25mg USD 400 In stock
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Quality Control & Documentation
Biological Activity

SR-717 is a non-nucleotide STING agonist with EC50s of 2.1 μM and 2.2 μM in ISG-THP1 (WT) and ISG-THP1 cGAS KO (cGAS KO) cell lines, respectively. SR-717 promoted the activation of CD8+ T, natural killer, and dendritic cells in relevant tissues. SR-717 also induced the expression of clinically relevant targets, including programmed cell death 1 ligand 1 (PD-L1), in a STING-dependent manner.

Product Citations
Protocol (for reference only)
Cell Experiment
Cell lines Bone marrow cells
Preparation method Following 8 days of differentiation, the cells were treated with free SR-717, HAC NPs, or HACS NPs (SR-717 concentration of 50 mg/L) at 37 °C for 24 h. After treatment, the cells were harvested, washed with PBS, and stained with antibodies CD11c, CD86, CD80, CD40, MHC-I, and MHC-II.
Concentrations 50 mg/L
Incubation time 24 h
Animal Experiment
Animal models C57BL/6 mice
Formulation 50% PEG300 and 50% saline
Dosages 30 mg/kg
Administration Injected intraperitoneally
Chemical Information
Molecular Weight 351.19
Formula C15H8F2LiN5O3
CAS Number 2375421-09-1
Solubility (25°C) DMSO 35 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Emily N Chin, et al. Science. Antitumor activity of a systemic STING-activating non-nucleotide cGAMP mimetic

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Keywords: SR-717, SR-717 lithium supplier, STING, inhibitors, activators

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