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LTβR-IN-1是一种有作用的、具有选择性的淋巴素β受体(LTβR)抑制剂。LTβR-IN-1 对TNF12A 的的 p52 的核易位抑制作用具有选择性,对 TNF-α 受体介导的 p65 的核易位无明显作用,却抑制受 TWEAK 或 Anti-LTβR 刺激的 p52 核易位,IC50为10 μM。LTβR-IN-1通过配体非依赖性方式实现对 NF-kB 信号通路的调节作用。
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LTβR-IN-1是一种有作用的、具有选择性的淋巴素β受体(LTβR)抑制剂。LTβR-IN-1 对TNF12A 的的 p52 的核易位抑制作用具有选择性,对 TNF-α 受体介导的 p65 的核易位无明显作用,却抑制受 TWEAK 或 Anti-LTβR 刺激的 p52 核易位,IC50为10 μM。LTβR-IN-1通过配体非依赖性方式实现对 NF-kB 信号通路的调节作用。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 297 | In stock | |
5 mg | ¥ 732 | In stock | |
10 mg | ¥ 1,180 | In stock | |
25 mg | ¥ 2,330 | In stock | |
50 mg | ¥ 3,340 | In stock | |
100 mg | ¥ 4,660 | In stock | |
500 mg | ¥ 9,360 | In stock | |
1 mL x 10 mM (in DMSO) | ¥ 798 | In stock |
LTβR-IN-1 相关产品
产品描述 | LTβR-IN-1 is a potent and selective lymphin β receptor (LTβR) inhibitor. LTβR-IN-1 has a selective inhibitory effect on the nuclear translocation of p52 of TNF12A, and has no obvious effect on the nuclear translocation of p65 mediated by TNF-α receptor, but inhibits the nuclear translocation of p52 stimulated by TWEAK or Anti-LTβR. Translocation with IC50 of 10 μM. LTβR-IN-1 regulates the NF-kB signaling pathway through a ligand-independent manner. |
靶点活性 | LTβR (p52 translocation):10 μM , LTβR (p52 translocation):0.169 μM |
分子量 | 320.35 |
分子式 | C18H16N4O2 |
CAS No. | 2189366-77-4 |
Smiles | C[C@@H](N1Cc2ccccc2C1=O)C(=O)Nc1nc2ccccc2[nH]1 |
密度 | 1.424 g/cm3 (Predicted) |
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: 113 mg/mL (350 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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