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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
STING agonist-22 (CF501) is a potent non-nucleotide STING agonist. STING agonist-22 is a adjuvant by activating STING to induce the type I interferon (IFN-I) response and proinflammatory cytokine production. STING agonist-22 can be used as an adjuvant to boost the original protein vaccine, producing potent, broad, and long-term immune protection. STING agonist-22 can be used for SARS-CoV-2 variants and sarbecovirus diseases research.
In Vitro
STING agonist-22 (CF501) leads to rapid and robust activation of innate immune responses in THP-1 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
STING agonist-22 (CF501) robustly, but transiently, activates innate immunity with acceptable safety profile in mice . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Balb/c mice (female, six weeks old) Dosage: 20, 75 μg Administration: Intramuscular injection Result: Although innate immunity was activated only transiently by CF501, it should be sufficient to stimulate the required humoral and cellular immune responses. The half-life of CF501 was 0.5 h and there was no detectable CF501 in the plasma after 2 h of the injection.
Form:Solid
| Sonrisas canónicas | NC(C1=CC2=C(N=C1)N(C/C=C/CN3C(NC(C4=CC(C)=NN4CC)=O)=NC5=C3C(OCCCN6CCOCC6)=CC(C(N)=O)=C5)C(NC(C7=CC(C)=NN7CC)=O)=N2)=O |
|---|---|
| Peso molecular | 820.90 |
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