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Bindarit (AF2838)是一种芳基烃受体(AHR)拮抗剂,在人胶质母细胞瘤U87细胞系中的IC50值为 39.9 nM。BAY-218 抑制 AhR 在体外刺激促炎单核细胞和 T 细胞反应,并驱动抗肿瘤免疫反应,导致体内肿瘤生长减少。


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Bindarit (AF2838)是一种芳基烃受体(AHR)拮抗剂,在人胶质母细胞瘤U87细胞系中的IC50值为 39.9 nM。BAY-218 抑制 AhR 在体外刺激促炎单核细胞和 T 细胞反应,并驱动抗肿瘤免疫反应,导致体内肿瘤生长减少。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 258 | In stock | |
| 2 mg | ¥ 365 | In stock | |
| 5 mg | ¥ 622 | In stock | |
| 10 mg | ¥ 997 | In stock | |
| 25 mg | ¥ 2,390 | In stock | |
| 50 mg | ¥ 3,620 | In stock | |
| 100 mg | ¥ 5,220 | In stock | |
| 500 mg | ¥ 10,900 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 658 | In stock |
BAY-218 相关产品
| 产品描述 | Bindarit (AF2838)is an aryl hydrocarbon receptor (AHR) antagonist with IC50 of 39.9 nM in the human glioblastoma U87 cell line. BAY-218 inhibition of AhR stimulates pro-inflammatory monocyte and T cell responses in vitro and drives anti-tumor immune responses, leading to reduced tumor growth in vivo. |
| 靶点活性 | AHR (U87 cells):39.9 μM, AhR (human cell lines):39.9 nM, CYP1A1 (U937 cells):70.7 μM |
| 体外活性 | 方法:Bindarit (AF2838)(1 nM、3nM、10nM、30nM、100nM、300nM、1 μΜ 和 3μΜ)处理人单核细胞 U937 细胞并测定 IC50 值。 |
| 体内活性 | 方法:Bindarit (AF2838)(30 mg/kg,口服,每日两次)和aPD-L1(10mg/kg,腹腔注射,每日两次)治疗侧腹皮下注射CT26肿瘤细胞的异种移植小鼠,观察其抗肿瘤能力。 |
| 别名 | AHR antagonist 1 |
| 分子量 | 401.82 |
| 分子式 | C20H17ClFN3O3 |
| CAS No. | 2162982-11-6 |
| Smiles | C[C@@H](CO)NC(=O)c1cc(nn(-c2cccc(F)c2)c1=O)-c1ccc(Cl)cc1 |
| 密度 | 1.37 g/cm3 (Predicted) |
| 存储 | store at low temperature,keep away from moisture | 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: 252 mg/mL (627.15 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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