CAS NO: | 329198-87-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | C-178 is a potent and selective covalent inhibitor ofSTING. C-178 binds to Cys91 and suppresses theSTINGresponses elicited by distinct bona fide activators in mouse but not human[1]. | ||||||||||||||||
IC50& Target | STING[1] | ||||||||||||||||
体外研究 (In Vitro) | 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[1].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[1].C-178 (1 μM; 1 hour) decreases cdG, dsDNA, CMA and LPS-inducedIfnb1expression in mouse bone marrow-derived macrophages[1].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[1]. Western Blot Analysis[1]
RT-PCR[1]
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分子量 | 322.27 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H10N2O5 | ||||||||||||||||
CAS 号 | 329198-87-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 41.67 mg/mL(129.30 mM;Need ultrasonic) 配制储备液
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