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diABZI STING agonist-1 (Tautomerism)

diABZI STING agonist-1 (Tautomerism)
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Purity:99.72%
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diABZI STING agonist-1 (Tautomerism)

Catalog No. T11035Cas No. 2138498-18-5
diABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.
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Pack SizePriceAvailabilityQuantity
1 mg$168In Stock
2 mg$265In Stock
5 mg$502In Stock
10 mg$678In Stock
25 mg$1,425In Stock
50 mg$2,350In Stock
100 mg$3,560In Stock
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Product Introduction

Bioactivity
Description
diABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.
In vitro
diABZI STING agonist-1 (Tautomerism) is a selective stimulator of interferon gene (STING) receptor agonists, with EC50 of 130 and 186 nM for humans and mice, respectively. diABZI STING agonist-1 (Tautomerism) at a concentration of 1 μM showed high selectivity for more than 350 kinases tested[1].
In vivo
diABZI STING agonist-1 (Tautomerism)(subcutaneous injection; 2.5 mg/kg) induces STING-dependent activation of type I interferon and proinflammatory cytokines in vivo. diABZI STING agonist-1 (Tautomerism) (intravenous; 3 mg/kg) exhibited systemic exposure with a half-life of 1.4 hours and reached a systemic concentration greater than half the maximum effective concentration of STING in mice (EC50) 200 ng/kg) ml). diABZI STING agonist-1 (Tautomerism) (intravenous; 1.5 mg / kg; 43 days) can significantly inhibit tumor growth and significantly improve survival rate (P <0.001). Eight out of 10 mice are tumor-free[1].
AliasdiABZI STING agonist (Compound 3)
Chemical Properties
Molecular Weight849.94
FormulaC42H51N13O7
Cas No.2138498-18-5
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years
Solubility Information
DMSO: < 1 mg/mL (insoluble), Sonication is recommended.

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