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Synonyms: diABZI STING agonist (Compound 3)

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $148 | In Stock | In Stock | |
| 2 mg | $218 | In Stock | In Stock | |
| 5 mg | $372 | In Stock | In Stock | |
| 10 mg | $533 | In Stock | In Stock | |
| 25 mg | $786 | In Stock | In Stock | |
| 50 mg | $1,080 | In Stock | In Stock | |
| 100 mg | $1,460 | - | In Stock | |
| 200 mg | $1,980 | - | In Stock |
| Description | diABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) is a selective agonist of the interferon gene-stimulated receptor (STING), with EC50 values of 130 nM in humans and 186 nM in mice. diABZI STING agonist-1 tautomerism is a tautomer of diABZI STING agonist-1. diABZI STING agonist-1 tautomerism can be used in research on tumor immunity, antiviral activity, and autoimmune diseases. |
| Targets & IC50 | STNG (human, PBMC cells):130 nM (EC50), H69AR cells:0.035 μM (EC50), STNG (mouse):186 nM (EC50), H69AR cells:0.055 μM (EC50) |
| In vitro | Methods: Add 0–10 μM diABZI STING agonist-1 (Tautomerism) to THP-1 cells, treat for 2–4 h, and detect pSTING and pIRF3 expression by Western blot. Results: Treatment with diABZI STING agonist-1 (Tautomerism) upregulates pSTING and pIRF3 expression. [1] |
| In vivo | Methods: To investigate the anticancer effects of diABZI STING agonist-1 (Tautomerism), a BALB/c mouse CT-26 colon cancer model was established. Following successful inoculation, diABZI STING agonist-1 (Tautomerism) was administered intravenously at 30 μg/mouse on days 0, 3, and 6. Results: Treatment with diABZI STING agonist-1 (Tautomerism) resulted in significant tumor suppression, with complete regression observed in some mice, persisting more than for 60 days. [1] |
| Synonyms | diABZI STING agonist (Compound 3) |
| Molecular Weight | 849.94 |
| Formula | C42H51N13O7 |
| Cas No. | 2138498-18-5 |
| Smiles | C(/C=C/CN1C=2C(N=C1NC(=O)C=3N(CC)N=C(C)C3)=CC(C(N)=O)=CC2OC)N4C=5C(N=C4NC(=O)C=6N(CC)N=C(C)C6)=CC(C(N)=O)=CC5OCCCN7CCOCC7 |
| Relative Density. | 1.44 g/cm3 (Predicted) |
| Storage | Store at low temperature,Keep away from direct sunlight,The compound is unstable in solution. Please use soon Powder: -20°C for 3 years Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 100 mg/mL (117.66 mM), Sonication is recommended. (The compound is unstable in solution, please use soon.) | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | ||||||||||||||||||||||||||||||||||||
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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