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|---|---|---|---|---|---|---|---|
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{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
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| 描述 | C-178 functions as a powerful and specific covalent inhibitor targeting STING. It forms a bond with Cys91, effectively dampening STING reactions triggered by various authentic activators in mice but not in humans [1]. |
| 体外研究 | C-178 focuses on the less understood N-terminal section of mmSTING, encompassing the transmembrane domains. Furthermore, it disrupts this mechanism by blocking STING's palmitoylation. Importantly, C-178 doesn't significantly impact STING reactions in human cells [1]. C-178 (0-1 μM; 1 hour) alone has minimal impact on the gene expression profile of BMDMs. Furthermore, it blocks the CMA-induced phosphorylation of TBK1 [1]. C-178 (1 μM; 1 hour) reduces the expression of Ifnb1 induced by cdG, dsDNA, CMA, and LPS in mouse bone marrow-derived macrophages [1]. C-178 (1 μM; 0.5-4 hours) suppresses the time-dependent induction of p-TBK1 and STING protein expression triggered by CMA in mouse embryonic fibroblasts [1]. |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
3.10mL 0.62mL 0.31mL |
15.51mL 3.10mL 1.55mL |
31.03mL 6.21mL 3.10mL |
|
| CAS号 | 329198-87-0 |
| 分子式 | C17H10N2O5 |
| 分子量 | 322.27 |
| SMILES Code | O=C(C1=CC=C([N+]([O-])=O)O1)NC2=CC=C3C(OC4=CC=CC=C34)=C2 |
| MDL No. | MFCD01146392 |
| 别名 | STING inhibitor C-178 |
| 运输 | 蓝冰 |
| InChI Key | URUVDCCYSJEGQQ-UHFFFAOYSA-N |
| Pubchem ID | 2866412 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 40 mg/mL(124.12 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
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