中文名称: | C-178 | ||||
---|---|---|---|---|---|
英文名称: | C-178 | ||||
别名: | C178;N-(Dibenzo[b,d]furan-3-yl)-5-nitrofuran-2-carboxamide; N-Dibenzofuran-3-yl-5-nitrofuran-2-carboxamide; N-3-Dibenzofuranyl-5-nitro-2-furancarboxamide;2-Furancarboxamide,N-3-dibenzofuranyl-5-nitro-;STING inhibitor C-178 | ||||
CAS No: | 329198-87-0 | 分子式: | C17H10N2O5 | 分子量: | 322.27 |
CAS No: | 329198-87-0 | ||||
分子式: | C17H10N2O5 | ||||
分子量: | 322.27 |
包装规格:
2mg 5mg 10mg 25mg 50mg 100mg in glass bottle
产品简介:
C-178 是 STING 的有效和选择性共价抑制剂。C-178 与 Cys91 结合,并抑制小鼠中而非人中由不同的激活剂引起的 STING 反应。
溶解性:
溶于DMSO (41.67 mg/mL)
储备液保存:
-80°C, 2 years
-20°C, 1 year
-20°C, 1 year
靶点:
STING
体外研究:
C-178 targets the poorly characterized N-terminal portion of mmSTING that includes the transmembrane domains. Moreover, C-178 interferes with this process by inhibiting the palmitoylation of STING. C-178 does not appreciably affect STING responses in human cells.
C-178 (0-1 μM; 1 hour) alone does not appreciably affect the gene expression profile of BMDMs. In addition, it inhibits the CMA-induced phosphorylation of TBK1.
C-178 (1 μM; 1 hour) decreases cdG, dsDNA, CMA and LPS-induced Ifnb1 expression in mouse bone marrow-derived macrophages.
C-178 (1 μM; 0.5-4 hours) inhibits the CMA-induced p-TBK1 and sting protein expression as a time-dependent manner in mouse embryonic fibroblasts.
C-178 (0-1 μM; 1 hour) alone does not appreciably affect the gene expression profile of BMDMs. In addition, it inhibits the CMA-induced phosphorylation of TBK1.
C-178 (1 μM; 1 hour) decreases cdG, dsDNA, CMA and LPS-induced Ifnb1 expression in mouse bone marrow-derived macrophages.
C-178 (1 μM; 0.5-4 hours) inhibits the CMA-induced p-TBK1 and sting protein expression as a time-dependent manner in mouse embryonic fibroblasts.
保存条件:
-20°C
注意事项:
1、为了您的安全和健康,请穿实验服并戴一次性手套操作。
2、以上信息仅做参考交流之用。
2、以上信息仅做参考交流之用。
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