中文名 | C-176 |
英文名 | N-(4-iodophenyl)-5-nitrofuran-2-carboxamide |
别名 | 化合物C-176 N-(4-碘苯基)-5-硝基-2-呋喃甲酰胺 N-(4-碘苯基)-5-硝基呋喃-2-甲酰胺 |
英文别名 | C-176 STING inhibitor 1 C-176 STING inhibitor N-(4-iodophenyl)-5-nitro-2-furamide N-(4-iodophenyl)-5-nitrofuran-2-carboxamide 2-Furancarboxamide, N-(4-iodophenyl)-5-nitro- |
CAS | 314054-00-7 |
化学式 | C11H7IN2O4 |
分子量 | 358.09 |
密度 | 1.935±0.06 g/cm3(Predicted) |
沸点 | 361.2±37.0 °C(Predicted) |
溶解度 | 溶于DMSO (高达25 mg/ml) |
酸度系数 | 11.14±0.70(Predicted) |
存储条件 | 2-8°C(protect from light) |
稳定性 | 从提供的购买之日起稳定1年。DMSO中的溶液可以在-20 °C下储存长达3个月。 |
外观 | 固体 |
颜色 | Brown or yellow |
体外研究 | C-176 strongly reduces STING-mediated, but not RIG-I- or TBK1-mediated, IFNβ reporter activity. Pretreatment with C-176 markedly reduce the CMA-mediated induction of serum levels of type I IFNs and IL-6. |
体内研究 | C-176 (750/375 nmol C-176 per mouse in 200 μL corn oil) significantly reduces the CMA-mediated induction of serum levels of type I IFNs and IL-6., without significant toxicity. C-176 results in a significant reduction in serum levels of type I IFNs and in a strong suppression of inflammatory parameters in the heart, with no evident signs of overt toxicity Trex1 −/− mice. C-176 demonstrates marked amelioration of various signs of systemic inflammation in Trex1 −/− mice. Animal Model: WT type mice. Dosage: 750/375 nmol C-176 per mouse in 200 μL corn oil (~1.34/0.67 mg/mL). Administration: Intraperitoneally, once. Result: Significantly reduced Serum levels of type I IFNs and IL-6. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.793 ml | 13.963 ml | 27.926 ml |
5 mM | 0.559 ml | 2.793 ml | 5.585 ml |
10 mM | 0.279 ml | 1.396 ml | 2.793 ml |
5 mM | 0.056 ml | 0.279 ml | 0.559 ml |
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