Chemical Structure : INI3069
货号: PC-27088Not For Human Use, Lab Use Only.
INI3069 is a human-selective STING agonist, inhibits trafficking of STING to the Golgi and blocks STING-mediated TFEB dephosphorylation and autophagy, enhances both humoral responses to co-administered antigen and anti-tumor responses.
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INI3069 is a human-selective STING agonist, inhibits trafficking of STING to the Golgi and blocks STING-mediated TFEB dephosphorylation and autophagy, enhances both humoral responses to co-administered antigen and anti-tumor responses.
INI3069 induce STING- and IRF3-dependent but ATG5-independent antiviral activity.
INI3069 suppressed CHIKV in THF-MAVS/TRIF−/− (IC50=0.6758 μM) and THF-ATG5−/− cells (IC50 = 0.5171 μM).
INI3069 elicits phosphorylation of TBK1 that was enhanced in STING+/+ and measurable in STING−/− cells.
INI3069 does not bind to the STING cytosolic domain and requires an intact TMD oligomerization domain for activation.
INI3069 blocks agonist-mediated Golgi trafficking and STING-mediated autophagy.
INI3069 blocks STING-mediated TFEB dephosphorylation and autophagy.
INI3069 enhances both humoral responses to co-administered antigen and anti-tumor responses.
INI3069 induces different molecular and immune effects compared to conventional STING agonists.
| 分子量 | 476.45 | |
| 分子式 | C23H16F4N2O3S | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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1. Mizuno N, et al. Cell Rep. 2026 Jun 1;45(6):117475.
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