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STING agonist-45

STING agonist-45 is a selective STING agonist (EC50 = 0.28 μM) . STING agonist-45 activates the innate immune response through the cGAS-STING pathway, upregulating key markers such as p-TBK1 and IRF3. STING agonist-45 exhibits robust STING activation in human peripheral blood mononuclear cells (PBMCs), inducing the production of type I interferons (such as IFN-β) and downstream cytokines (such as TNF-α and IL-6) . STING agonist-45 enhances anti-tumor immunity, inhibits tumor growth, and increases CD8+ T cell infiltration in mouse models. STING agonist-45 is promising for the study of STING-related diseases[1][2].

Product Specifications

CAS Number

[2361424-97-5]

UNSPSC

12352005

Target

Cyclic GMP-AMP Synthase; IFNAR; Interleukin Related; STING; TNF Receptor

Related Pathways

Apoptosis; Immunology/Inflammation

Field of Research

Cancer; Inflammation/Immunology

Smiles

O=C(C1=CC2=C(C(OC3COC3)=C1)N(CCC)C(NC(C4=CC(C)=NN4CC)=O)=N2)N

Molecular Formula

C21H26N6O4

Molecular Weight

426.47

References & Citations

[1]Shan B, et al. Design, Synthesis, and Biological Evaluation of Bipyridazine Derivatives as Stimulator of Interferon Genes (STING) Receptor Agonists. J Med Chem. 2023 Mar 9;66 (5) :3327-3347.|[2]Jin Li, et al. Immunomodulator, WO2019134707A1.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Curated Selection

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