hSTING activator-1 (Compound 68) is a STING agonist. hSTING activator-1 can effectively activate multiple human STING variants (R232, H232, HAQ) with EC50 values of 56 nM, 89 nM and 51 nM, respectively. hSTING activator-1 activates the type I interferon pathway by directly binding to STING protein and stabilizing its conformation, promoting downstream IRF3 phosphorylation and cytokine release. hSTING activator-1 inhibits fibrosarcoma tumor growth and has potential in cancer research[1].
Molekulargewicht:
470.52
Formel:
C26H19FN4O2S
Target-Kategorie:
IFNAR,Interleukin Related,STING
Anwendungsbeschreibung:
MCE Product type: Reference compound1
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