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diABZI STING agonist-1 (Tautomerism)

(Synonyms: diABZI STING agonist (Compound 3)) Copy Product Info
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Synonyms: diABZI STING agonist (Compound 3)

Catalog No. T11035 Copy Product Info
Purity: 99.72%
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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.
diABZI STING agonist-1 (Tautomerism)
Cas No. 2138498-18-5
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$148In StockIn Stock
2 mg$218In StockIn Stock
5 mg$372In StockIn Stock
10 mg$533In StockIn Stock
25 mg$786In StockIn Stock
50 mg$1,080In StockIn Stock
100 mg$1,460-In Stock
200 mg$1,980-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.72%
Appearance:Solid
Color:White to Yellow
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Product Introduction

Bioactivity
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]
SynonymsdiABZI STING agonist (Compound 3)
Chemical Properties
Molecular Weight849.94
FormulaC42H51N13O7
Cas No.2138498-18-5
SmilesC(/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 & Solubility Information
StorageStore 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
1mg5mg10mg50mg
1 mM1.1766 mL5.8828 mL11.7655 mL58.8277 mL
5 mM0.2353 mL1.1766 mL2.3531 mL11.7655 mL
10 mM0.1177 mL0.5883 mL1.1766 mL5.8828 mL
20 mM0.0588 mL0.2941 mL0.5883 mL2.9414 mL
50 mM0.0235 mL0.1177 mL0.2353 mL1.1766 mL
100 mM0.0118 mL0.0588 mL0.1177 mL0.5883 mL
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.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
% DMSO
%
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Dose Conversion

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Keywords

Related Tags: diABZI STING agonist-1 (Tautomerism) chemical structure | diABZI STING agonist-1 (Tautomerism) in vivo | diABZI STING agonist-1 (Tautomerism) in vitro | diABZI STING agonist-1 (Tautomerism) formula | diABZI STING agonist-1 (Tautomerism) molecular weight