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TNF-α-IN-18是一种肿瘤坏死因子-α (TNF-α) 的抑制剂,其 IC50 为 1.8µM。TNF-α-IN-18有效阻断核因子 κB (NF-κB) 的核转位,从而抑制下游 TNF 信号通路。在小鼠成纤维 LM 细胞中表现出最小细胞毒性 (CC50 大于 50 µM)。研究证实 TNF-α-IN-18 能缓解小鼠模型中 TNF 或脂多糖诱导的脓毒症,并对类风湿关节炎的发展提供显著保护作用。
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TNF-α-IN-18是一种肿瘤坏死因子-α (TNF-α) 的抑制剂,其 IC50 为 1.8µM。TNF-α-IN-18有效阻断核因子 κB (NF-κB) 的核转位,从而抑制下游 TNF 信号通路。在小鼠成纤维 LM 细胞中表现出最小细胞毒性 (CC50 大于 50 µM)。研究证实 TNF-α-IN-18 能缓解小鼠模型中 TNF 或脂多糖诱导的脓毒症,并对类风湿关节炎的发展提供显著保护作用。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 158 | In stock | |
5 mg | ¥ 343 | In stock | |
10 mg | ¥ 548 | In stock | |
25 mg | ¥ 879 | In stock | |
50 mg | ¥ 1,380 | In stock | |
100 mg | ¥ 2,250 | In stock | |
200 mg | ¥ 3,360 | In stock |
TNF-α-IN-18 相关产品
产品描述 | TNF-α-IN-18 (Compound 61) is a small molecule inhibitor of tumor necrosis factor-alpha (TNF-α) that operates with a IC50 of 1.8µM. TNF-α-IN-18 effectively blocks the nuclear translocation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), thereby suppressing the downstream TNF signaling pathway; TNF-α-IN-18 exhibits minimal cytotoxicity in mouse fibroblast LM cells with a CC50 greater than 50 µM. TNF-α-IN-18has been shown to alleviate sepsis induced by TNF or lipopolysaccharide in mouse models, and provides significant protection against the development and progression of rheumatoid arthritis in murine models. |
分子量 | 336.67 |
分子式 | C16H7ClF2O4 |
CAS No. | 1272322-42-5 |
Smiles | O=C(O)C=1C(=O)C2=CC=C(Cl)C=C2OC1C=3C=C(F)C=CC3F |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 80 mg/mL (237.62 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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