C-176 98%

N-(4-iodophenyl)-5-nitrofuran-2-carboxamide

源葉(MedMol)
S88645
314054-00-7
C11H7IN2O4
358.08875
品牌 貨號(hào) 產(chǎn)品規(guī)格 價(jià)格(RMB) 庫(kù)存(上海) 北京 武漢 南京 購(gòu)買(mǎi)數(shù)量
源葉(MedMol) S88645-5mg 98% ¥450.00元 3 - - -
源葉(MedMol) S88645-10mg 98% ¥780.00元 2 - - -
源葉(MedMol) S88645-25mg 98% ¥1360.00元 5 - - -
源葉(MedMol) S88645-50mg 98% ¥1904.00元 預(yù)計(jì)交期:2-3天 - - -
源葉(MedMol) S88645-100mg 98% ¥2720.00元 預(yù)計(jì)交期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn)(1篇) 質(zhì)檢證書(shū)(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

STING inhibitor C-176是一種有效的STING抑制劑。STING是細(xì)胞內(nèi)DNA感應(yīng)通路的主要信號(hào)分子
產(chǎn)品描述: STING inhibitor C-176是一種有效的STING抑制劑。STING是細(xì)胞內(nèi)DNA感應(yīng)通路的主要信號(hào)分子
靶點(diǎn): STING
體外研究: C-176 strongly reduces STING-mediated, but not RIG-I- or TBK1-mediated, IFNβ reporter activity. It directly targets mouse STING (mmSTING) but not human STING (hsSTING)
體內(nèi)研究: C-176 attenuates STING-associated autoinflammatory disease in mice
細(xì)胞實(shí)驗(yàn): Cell lines: H526 cells Concentrations: 1?μM Incubation Time: 48 h Method: Cells were treated 1 μM C176 and 1 μM AZD1775 for 48 h
動(dòng)物實(shí)驗(yàn): Cell lines: H526 cells Concentrations: 1?μM Incubation Time: 48 h Method: Cells were treated 1 μM C176 and 1 μM AZD1775 for 48 h
參考文獻(xiàn): 1. Haag SM, et al. Targeting STING with covalent small-molecule inhibitors, Nature. 2018, 559(7713):269-273. 2. Taniguchi H, et al. WEE1 inhibition enhances the antitumor immune response to PD-L1 blockade by the concomitant activation of STING and STAT1 pathways in SCLC. Cell Rep. 2022 May 17;39(7):110814.
溶解性: Soluble  in  DMSO、Ethanol
保存條件: -20°C
配置溶液濃度參考:
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
50 mM 0.056 ml 0.279 ml 0.559 ml
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質(zhì)檢證書(shū)(COA)

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摩爾濃度計(jì)算器

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