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STING agonist-3

Cat. No. M14124

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STING agonist-3 Structure
Size Price Availability Quantity
1mg USD 165 In stock
5mg USD 360 In stock
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Quality Control & Documentation
Biological Activity

STING agonist-3 is a selective and non-nucleotide small-molecule STING agonist with a pEC50 and pIC50 of 7.5 and 9.5, respectively. STING agonist-3 has durable anti-tumor effect and tremendous potential to improve treatment of cancer.

Chemical Information
Molecular Weight 750.81
CAS Number 2138299-29-1
Solubility (25°C) DMSO 40 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Ru-Yan Zhang, et al. A protein vaccine with Alum/c-GAMP/poly(I:C) rapidly boosts robust immunity against SARS-CoV-2 and variants of concern

[2] Markta Pimkov Polidarov, et al. Synthesis and Biological Evaluation of Phosphoester and Phosphorothioate Prodrugs of STING Agonist 3',3'-c-Di(2'F,2'dAMP)

[3] Michael A Collier, et al. Acetalated Dextran Microparticles for Codelivery of STING and TLR7/8 Agonists

[4] Chih-Hang Anthony Tang, et al. Agonist-Mediated Activation of STING Induces Apoptosis in Malignant B Cells

Related STING Products
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Vadimezan (DMXAA; ASA-404) acts as a tumor vascular disrupting agent (tumor-VDA), is also a murine agonist of the stimulator of interferon genes (STING) and also a potent inducer of type I IFNs and other cytokines.

G10

G10 is a activator of STING-dependent signaling.

3′3′-cGAMP

3',3'-cGAMP is an endogenous second messenger in metazoans and triggers interferon production in response to cytosolic DNA. 3',3'-cGAMP activates stimulator of interferon genes (STING), which activates a signaling cascade leading to the production of type I interferons and other immune mediators.

diABZI (tautomerism)

diABZI (STING agonist 1; Tautomerism) is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.

C-176

C-176 is a potent, selective and blood-brain barrier permeable inhibitor of STING. C-176 covalently targets transmembrane cysteine residue 91 and thereby blocking activation-induced palmitoylation of STING.

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Keywords: STING agonist-3 supplier, STING, inhibitors, activators

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